Prostate Cancer Research and Treatment

For Karl Loren

Link to LIST of Dark Times Digests and Related Items

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Karl Note: You can simply read straight down, or pick from the various segments listed below to jump back and forth between the segment and this top of the page.

Personal

1.1 Personal Vital Statistics: Daily Weight, BP and other

1.2 Karl's first indication that he might have prostate cancer

1.3 Karl's further Considerations after a few days of thought

1.4 Karl's final, and changing, total advice about his own treatment

1.5 Karl's Photo Slide Show -- Never Before Published

1.55 Or 1.12 OR SUCH Will be used to add items in the sequence and allow the existing number sequence to be relatively stable

1.6 eMail Exchanges With Karl and Subscribers about prostate health

1.7 LRH Quotes

 

 

Drugs

2.1 Data about Avodart

2.2 Data about Uroxatral®

2.3 Solage liquid for skin conditions including skin cancer

2.x Additional Drug Information

 

 

Treatments:

3.1 PSA Test Official Government Data

3.2 "Official" FDA Description of this Prostate Health Problem

3.3 Prostate Cancer Treatment Choices

3.31 Prostate Draining and "Milking"

3.4 My About-Face on the PSA Test Why every man should have this prostate test done today!

3.5 FAKE Source of Data About Prostate Cancer

3.6 Suggestion From Karl's Close Friend Dr. MSR Ayyangar, Mumbai, India

3.8 Vitamin D3 as a previously under appreciated prevention of cancer.

3.81 Vitamin D -- More details on it as a cancer preventative

3.9 Q&A About PSA Scores -- Doctor's Answers

 

 

3.XX For additional items

 

Suggested Protocol

4.1 Karl Loren's Treatment Protocol

 

1.2

 

The start, with the tentative diagnosis and immediate Plan for Karl Loren

Sent as an eMail to several people on 17 July 2009

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I, Karl Loren, had a routine physical examination on July 3, 2009, with the schedule for receiving the results on July 17, 2009, the very day I start writing this page.

While the results were "normal" and "not unusual" in all respects but one, that one gives me the motivation to write and publish this page.

That result was a PSA reading of 15.

Later that day I wrote the following message on Friday, July 17, 2009, to close friends, including Debbie, to give them some of the plan I expected to follow:

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Dear Debbie,

Thanks.

I'll give you a result from today's visit to our new family MD, Dr. Prance.

Blood and all looked good and normal, except

PSA reading of 15

He recommends two urologists -- one to test the reading, a general urologist, and if cancer is confirmed, then another at USC who is famous for his willingness to lay out all the various treatment possibilities, rather than, as most, have a fixed opinion about the ONLY treatment to be used.

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In the mean time I will start publishing a web page, as I did about Bonnie, including the research and results I find about Prostate Cancer.

and, I'll start taking

Germanium - same as Bonnie expects to take daily the rest of her life -- about 2/3 grams per day.

Taheebo - about the same as Bonnie took during her cancer and still takes every day.

I've also started 200 micrograms of Selenium daily

I will be looking into getting an alkaline water machine -- Owen Charles has one to suggest, I used to own one, and will also be revisiting my research and knowledge of such machines. Cancer cannot survive in an alkaline environment.

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I will be looking for the best source of Pycnogenol and or grape seed extract most probably to research a best source and a bulk supplier, then investigate what might be added to some of these ingredients to make a new product for VL.

It may well be that something of my creation, in part, with advice and suggestion from Dr. MSR Ayyangar, India, will be a good seller for VL and be useful for me.

Click here for final Protocol Advised by Dr. MSR Ayyangar and with Karl's further research.

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In the mean time I am greatly enjoying my research and writing about the economic mess and looking forward to making a difference on the planet.

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As I've been writing, and publishing so far, "All it takes is a massive dose of honesty among our politicians (and our public) and even the mad dreams of Obama could be implemented into the Golden Age."

I know the method by which that can be done, but the method of persuading people that this is a bigger and better game than the economic mess we are playing now?? That will be my skill as a researcher and writer -- looking forward to that.

Karl Loren

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On Fri, Jul 17, 2009 at 10:14 AM, Debbie wrote:

I understand and thank goodness you do. Too many people want small games. I was listening to a lecture Wed. night, where Ron says, if you don't learn anything learn Logic 6 and then the one after that which he emphasized was gradients. So we'll call it a gradient to get people more and more involved.

Keep up the good work.

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----- Original Message -----
From: Karl Loren
Sent: Wednesday, July 15, 2009 7:58 PM
Subject: Re: health care

Dear Debbie

The problem is MUCH bigger than any petition can solve.

I am still in progress in research and writing my newsletter about the new FDA Commissioner who will greatly increase legitimacy of psych drugs while making vitamins subject to regulation -- a gloomy picture.

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Take a look at:

http://www.vibrantlifellc.com/2/21.htm

Karl Loren

1.3

Two Days After: Considerations and Thoughts

Sunday, July 19, 2009

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My first thought at hearing the "PSA 15" was that I recognized what the significance was -- that about 3 or 4 was OK, 5 was of concern and over 12 was serious.

So, I first thought of this news as "serious," but in the same breath the doctor said "Prostate cancer hardly ever kills anyone -- they die of something else first, and it is also slow growing thing -- 10 years at least before it is ..."

I don't know what he said, but my thought at this point was, "Well, that's enough time to do all the things that I have planned to do."

Then I heard him say something like, "It gets very painful if not handled in time."

That made me want to get further data on that.

I looked.

I found, instead, what I consider deceptive web mastering where some person figures he can sell advertising on a particular "phrase" such as "end stage prostate cancer."

Indeed that is almost all I found. I finally accepted one of them, their text is HERE.

Their "home page," indeed, featured many links to doctors who must have paid to have their link there, and also many links where Google had placed ads of theirs (paid for by clients).

The entire web seems to be nothing more than a few articles, and ZERO information about the owners. The disclaimer at the bottom keeps them out of medical trouble, and can, itself, be a screen for the "doctors" who don't want their name associated with the text, but DO want the referrals from the page -- clever/nasty.

In this way Google is, itself, diluting the value of their web search, and enabling others to do the same -- all with the view of capturing the "eye ball" of the web searchers. Almost enough to make a person look for a different search engine.

The above, about search engines, was NOT what I expected to write here, but it is worth remark.

When you click on the link from that page, you will NOT find any reference to alternative remedies --- presumably someone could pay to have his "vitamin web site" shown on that page, but without any mention of alternatives, it would not be a useful place to spend ad money.

 

Back to my thoughts and considerations.

I conclude that "end stage prostate cancer" means the cancer has metastasized into the bones. I can understand how that might be painful, but the "watchful waiting" treatment I've already found HERE, suggests that regular PSA tests can indicate quickly enough, with a slow-growing cancer, if some treatment reduces the PSA test result -- thus indicating that the treatment, whatever it is, seems to be working.

It seems now that I am in for understanding the PSA tests much better, how to get them and which of any treatments reduces those scores.

After reading the government-sourced data about PSA tests, I conclude that the data is oriented very much, almost ONLY, toward using the PSA test for detecting CANCER, NOT for measuring the other possibility -- enlarged prostate gland.

One small piece of good news in the government data was this:

Currently, Medicare provides coverage for an annual PSA test for all men age 50 and older.

As of now I am further confirmed in my initial choice of using "watchful waiting" while "treating" the PSA reading as indicating "cancer," but "treating whatever it is with nothing more than non-drug and non-surgery and non-radiation types of treatments.

Another reference I found useful from the government data was this:

Because PSA levels tend to increase with age, the use of age-specific PSA reference ranges has been suggested as a way of increasing the accuracy of PSA tests. However, age-specific reference ranges have not been generally favored because their use may lead to missing or delaying the detection of prostate cancer in as many as 20 percent of men in their 60s and 60 percent of men in their 70s. Another complicating factor is that studies to establish the normal range of PSA values have been conducted primarily in white men. Although expert opinions vary, there is no clear consensus on the optimal PSA threshold for recommending a prostate biopsy for men of any racial or ethnic group. (source: Part of answer #4, here.)

Another encouraging comment follows:

These results suggest that many men were diagnosed with, and treated for, cancers that would not have been detected in their lifetime without screening and, as a consequence, were exposed to the potential harms of unnecessary treatments, such as surgery and radiation therapy. Nevertheless, it remains possible that a small benefit from the earlier detection of these “excess” cancers could emerge with longer follow-up. Follow-up of the PLCO participants will continue, therefore, until all participants have been followed for at least 13 years. (Source: Part of Answer to Question #9 here

 

The initial protocol is just as I have laid out in my first-day report to friends about what I expected to use -0- HERE.

 

1.4

Karl's Final Summary and his Plan of Treatment -- Changing regularly

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August 2, 2009

Re:  prostate test and other matters

 

Dr. D. W. Plance
2520 Honolulu Avenue
Suite 170
Montrose, CA 91020

Phone 818.249.4134
FAX 818.249.9523

Dear Dr Plance,

I have good news to report, both about the prostate and my blood pressure.

First, the BP:

 

Loren C. Troescher
Date Time SYS DIA Pulse Date Time SYS DIA Pulse
(mmHg) (mmHg) (Pulses/min) (mmHg) (mmHg) (Pulses/min)
08/02/2009 10:19:07 AM 156 81 65
08/02/2009 10:21:40 AM 147 77 62
08/02/2009 02:05:48 PM 181 92 81
08/02/2009 02:06:35 PM 171 85 78
08/02/2009 02:08:57 PM 160 82 72
08/02/2009 02:09:59 PM 154 85 74
08/02/2009 02:11:07 PM 162 82 71
08/02/2009 07:16:37 PM 143 78 86
08/02/2009 07:17:14 PM 125 70 82
08/02/2009 07:17:54 PM 134 69 84
08/02/2009 07:18:34 PM 138 74 86

I’ve pasted in above some of the readings done today.  They show, for each day, more so after the sample I sent to you by mail, SOME readings every day that were below 150/100, including one today, shown in bold type.

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I use the BP machine generally always with the same procedure:  I measure while sitting at my desk, often cold because of the AC.  Once I get a low reading, I typically repeat the test several times during the next few minutes.

It appears that I can always get a reading at or below 150/100 by relaxing more or getting warm, or sitting “better” at the desk. It also seems that certain times of the day are more likely to produce lower scores.

It seems to me that the new BP med is doing the job.
Thanks for that sample.  I need the new prescription so I can get more pills – I am soon out.

On the prostate, another good report.

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After my first visit with Dr. Reynolds I gave blood and urine samples and understood from him that the blood test would measure the “free PSA” percentage and that 30% or higher would typically indicate no cancer while 11% or less would be indication of probable cancer. The blood test lab assured me that your name on the test request meant you would receive a copy.

From Dr. Reynold’s rectal exam he described the prostate as very large but all soft with no hard parts. I do not seem to have any difficulty with urination. Night time frequency is not an issue when I sleep with my CPAK.  I forgot to mention to him, or you, that I had a very painful removal of a catheter after a failed stent placement required me to stay in the hospital overnight about a year ago.  The need for the catheter had not been anticipated, it had to be inserted and withdrawn with no sedation – very painful and it caused painful urination for some weeks.

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 That symptom is now gone.

My wife and I saw Dr. Reynolds last Friday to learn these test results.
You should have also received a copy from the lab for the blood test.
Dr. Reynolds was upbeat. He did not give me his final opinion until he had given me all the details.

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First, he said that I had come in with a blood test of PSA 15, and just exactly one week later, a second blood test showed that reading at 12 (I think that was the number).

He said that there is a known phenomenon of a PSA score that rises and falls in a pattern, so that further PSA tests would probably reveal the high and low points of a continuing pattern.  I didn’t get the exact significance of this “pattern,” but did get the idea that the fact that the score was significantly lower than a week earlier meant that there was considerably less to worry about with that reading, not so much that it was low (not so) but because it fluctuated.
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He next told us that the Free PSA  was (I think he said) 15.  That is not as high as the 30% score that indicates no cancer, but not as low as the 11% score that indicates a strong possibility of cancer.
He then said that looking at those test results, plus his own rectal exam which showed a greatly enlarged prostate, but no hard spots, and no reported difficulty with urination led him to his final opinion.
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He said that he felt the chances of cancer were a small amount less than 50%, and he used the term, “watchful” and suggested I do nothing.  No biopsy, and come back in several months for another Free PSA test – and to see if the prostate was larger or smaller.  That is now scheduled for early December, with a copy of the test result for you.

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I was pleased with that opinion, told him so, and told him that I fully expected to pursue non-drug remedies.

I described them to him == although I think he was simply polite and did not know about them, nor want to give any opinion.
He did say that he didn’t recommend any drug, and the only thing he could suggest would be a standard “heart-healthy” diet.

I told him my opinion about the dangers of a biopsy, causing a spread of cancer if there were any there.
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He (politely) disagreed, saying that there was no such danger relative to prostate – might be for other types of cancer, but not prostate – he then “threw in” that prostate was slow growing.  I suspect that any lack of evidence of biopsy-caused spreading is missed simply because prostate cancer is so slow.  I still would pursue other “serious” remedies” rather than move ahead with a biopsy or surgery or drugs.

He also told me that he knew of a Prostate test of selenium, but that it turned out to not be as useful as people had hoped.  I listen, but am taking 400 mcg of Selenium daily anyway.

I am taking about 1-2 grams of pure germanium daily, and the equivalent of about 40 of the Taheebo capsules every day.

I also take pycnogenol, grape seed extract, a Whole Foods prostate health formula.  I have also studied about, and probably will use,  “milking” the prostate to drain excess fluid and am willing to learn about other remedies you might suggest.

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The skin cancer usage of Solage seems to reduce the area of redness. 

One day I went some hours before application and it appeared to have “grown” to its earlier size.  It seems to respond to the twice-daily application.  I would be ready to get another bottle if this apparent improvement continues.

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I’ll call soon to find out if you think another visit to your office is called for.

 

 

Regards,
 
 
 
Loren C. Troescher

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1.5

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Karl Loren Slide Show -- Mostly unpublished photos

 

Click Here for Slide Show

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1.6

The LINK for the eMail messages with Karl is HERE.

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1.7

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LRH Quotes

 

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"When you can be your own best audience and when your applause is the best applause you know of, you're in good shape. And when you can play a real good role — when you can go down here and be the mule or be the general with equal verve, in the total spirit of play, and do it with terrific sincerity — you're living!"


— L. Ron Hubbard


Excerpted from the lecture Ability to Accept Direction, delivered on 21 December 1953.
This lecture can be found in the 2nd American Advanced Clinical Course lectures, otherwise known as the Rehabilitation of the Human Spirit.

 

"The next time you think you're having an awful lot of trouble somewhere, well, just wonder whether or not you can't communicate with it. And if you communicated with it gently enough, it won't backfire hard. If you communicate and—miscalculate a little bit and communicate too much or too fast or with too much velocity, it's liable to come back and knock your head off. But that's all right, put your head back on and communicate again. That's always what you must do. The reason you stopped communicating in the first place is you lost a few heads, but what are heads? Expendable."
— L. Ron Hubbard

 


Excerpted from the lecture Power of Choice and Self-Determinism, delivered on 29 October 1955.

2.1

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AVODART

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Source: Official Mfg

Karl Note Inserted: It appears from the adverse side effects listed below that this drug company may be withholding adverse information, and could be sued. I found them on the web at a bit less than $3.00 per pill..

Over time, AVODART can shrink the prostate. If left untreated, the prostate may continue to grow, and in some men lead to worsening urinary symptoms.

The benefits of AVODART can include:

  • Shrinking of the size of the prostate
  • Improving bothersome urinary symptoms
  • Long-term symptom improvement
  • Reducing the risk of developing acute urinary retention (AUR), the sudden inability to urinate
  • Reducing the risk of needing surgery for an enlarged prostate

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If you have Enlarging Prostate, talk to your doctor about shrinking it and ask if AVODART is right for you.

Adverse Side Effects:

Indication and Important Safety Information About AVODART® (dutasteride):
AVODART alone and in combination with the alpha blocker tamsulosin treats urinary symptoms of Enlarging Prostate. AVODART alone also reduces the risk of acute urinary retention (AUR) and prostate surgery. AUR is a condition, possibly requiring surgery, where the prostate is so enlarged that it completely blocks urine coming from the bladder.

Only your health care provider can tell if your symptoms are from Enlarging Prostate and not a more serious condition, such as prostate cancer.

See your doctor for regular exams.

Women and children should not take AVODART.

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Women who are or could become pregnant should not handle AVODART due to the potential risk of a specific birth defect.

Do not donate blood until at least 6 months after stopping AVODART.

Tell your doctor if you have liver disease.

AVODART may not be right for you.

Possible side effects, including sexual side effects and swelling or tenderness of the breast, occur infrequently. Dizziness and an increase in drug-related ejaculation disorders also occurred with combination therapy (AVODART and tamsulosin).

While some men have fewer problems and symptoms after 3 months of treatment with AVODART, a treatment period of at least 6 months is usually necessary to see if AVODART will work for you.

------------------------------ADVERSE REACTIONS-----------------------
The most common adverse reactions, reported in ≥1% of patients treated with AVODART and more commonly than in patients treated with placebo, are impotence, decreased libido, ejaculation disorders, and breast disorders. (6.1)
To report SUSPECTED ADVERSE REACTIONS, contact GlaxoSmithKline at 1-888-825-5249 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

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Monotherapy:
• The most common adverse reactions reported in subjects receiving AVODART were impotence, decreased libido, breast disorders (including breast enlargement and tenderness), and ejaculation disorders.
• Study withdrawal due to adverse reactions occurred in 4% of subjects receiving AVODART and 3% of subjects receiving placebo. The most common adverse reaction leading to study withdrawal was impotence (1%).

 

Non-Official Claims of Adverse Affects

Teratogenic effect

Wikipedia Source

(Affect on pregnant women of male children who even touch these)

The teratogenic effect from Dutasteride is a very large risk for male children. The effect would be similar to 5-alpha-reductase deficiency, where a developing male child naturally is deficient in 5-alpha reductase type 2, and thus unable to synthesize DHT Type 2. As Dutasteride blocks the same process (although type 1 and 2 DHT) a developing male would have this deficiency as a result of medication, rather than simply naturally.

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Women who are pregnant or in their childbearing years, and children, should be prevented from handling the capsules as inadvertent consumption may cause major birth defects.

Another Source for Adverse Effects

 

Adverse Events

Source

Twenty-five percent (102/416) of subjects experienced a total of 169 adverse events that were classified by the investigator as having a reasonable possibility of being drug-related (7). Those drug-related adverse events having and incidence > 5% within any treatment group are presented in Tale 2.

The most common drug-related adverse event were decreased lilbido experienced by 13% of subjects receiving Avodart 2.5 mg/day followed by headaches, experienced by 8% of the Avodart 0.1mg/day group and 6% by both the Avodart 0.5mg/day and 2.5 mg/day group. There were no serious adverse events that were considered drug-related.

Partner Pregnancies

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Five partner pregnancies were reported during the study. One female partner spontaneously aborted (study subject was on placebo) and one had a partial placenta previa with subsequent delivery of a normal male infant (study subject was on Avodart 0.5 mg). The other three pregnancies were normal and resulted in the births of two males (two subjects on "Avodart 0.5mg and one on Avodart 2.5mg) and one female (subject on Avodart 2.5mg). None of the infants had genital or other abnormalities at birth (7).

Precaution

Avodart Soft Gelatin Capsules should not be handled by a woman who is pregnant or who may become pregnant because of the potential for absorption of dutasteride and the subsequent potential risk to a developing male fetus. Avodart is contraindicated for use in women. Avodart has not been studied in women because preclinical data suggest that the suppression of circulation levles of dihydrotestosterone may inhibit the development of the external genital organs in a male fetus carried by a woman exposed to dutasteride (6) REV 0704

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Google Search Result (but the web demands your personal data before they will give the results claimed.)

Drug interactions analysis of Avodart, Uroxatral for males aged 60 ...

93 related reports are studied for females and males at all ages when co-using Avodart, Uroxatral: Comparison with the patient's adverse outcomes: ...

 

 

2.2

 

Uroxatral®

 

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Karl Note: I would certainly avoid using this drug -- first it is a "drug" when natural remedies, even "watchful waiting" seems better to me and second because of all the "side effects" which the drug maker does NOT include in his official warning. Mostly I find that even a person who wants to find the information I have on this page cannot find it without learning the tricks of the drug companies. They deliberately "own" OR "CREATE" dozens of web sites, different addresses, but hire expensive web designers, get high Google Search Engine Rankings and therefore these dominate the first 50 or so search results.

I had to wade through dozens of these deceptive web sites, many of them simply selling the pill and repeating the company's lies.

I, Karl Loren, not only research the drug itself, but the very method you might use to find out about it.

Beware! The web is changing in favor of the drug industry, and Google goes along with it while the FDA promotes it. See my expose of the new FDA Commissioner whose job it is and will be to make it easier for drugs to hit the market and to hit you.

Source: Official Site

Indication Uroxatral® (alfuzosin HCl 10 mg extended-release tablets) is an alpha1-blocker for the treatment of the signs and symptoms of BPH.

Important Safety Information

Do not take UROXATRAL if you have liver problems or if you are taking antifungal drugs like ketoconazole or itraconazole, or HIV drugs like ritonavir.

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UROXATRAL can cause a sudden drop in blood pressure, especially when starting treatment. This may lead to fainting, dizziness, and lightheadedness. Do not drive, operate machinery, or do any dangerous activity until you know how UROXATRAL will affect you. This is especially important if you already have a problem with low blood pressure or take medicines to treat high blood pressure. There may be an increased risk of low blood pressure and fainting when taking UROXATRAL in combination with blood pressure medication or nitrates.

Before taking UROXATRAL, tell your doctor if you have kidney problems.

Also, tell your doctor if you or any family member(s) have or take medications for a rare heart condition known as congenital prolongation of the QT interval.

BPH and prostate cancer can cause the same symptoms. However, UROXATRAL is not a treatment for prostate cancer.

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The most common side effects with UROXATRAL are dizziness, upper respiratory tract infection, headache, and tiredness.

Official Instructions:

INDICATIONS AND USAGE

UROXATRAL an alpha1-adrenoreceptor-antagonist, is indicated for the treatment of signs and symptoms of benign prostatic hyperplasia. UROXATRAL is not indicated for the treatment of hypertension.


DOSAGE AND ADMINISTRATION

10 mg once daily taken immediately after the same meal each day.

Tablets should not be chewed or crushed

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Official ADVERSE REACTIONS

Most common adverse reactions in clinical studies (incidence ≥2%): dizziness, upper respiratory infection, headache, fatigue. (6.1)

Adverse reactions reported during post-marketing experience include: angina pectoris in patients with pre-existing coronary artery disease, hepatocellular and cholestatic liver injury, priapism, angioedema (6.2)

Other adverse reactions have also been reported (6)

 

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FDA Warning --Women should not use:

alfuzosin hydrochloride or any component of UROXATRAL tablets.
WARNINGS
Postural hypotension with or without symptoms (e.g., dizziness) may develop within a few hours
following administration of UROXATRAL (alfuzosin HCl extended-release tablets). As with
other alpha-blockers, there is a potential for syncope. Patients should be warned of the possible
occurrence of such events and should avoid situations where injury could result should syncope
occur. There may be an increased risk of hypotension/postural hypotension and syncope when
taking UROXATRAL concomitantly with anti-hypertensive medication or nitrates. Care should
be taken when UROXATRAL is administered to patients with symptomatic hypotension or
patients who have had a hypotensive response to other medications.

 

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PRECAUTIONS

 

General

 

Prostatic Carcinoma: Carcinoma of the prostate and BPH cause many of the same symptoms.

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These two diseases frequently coexist. Therefore, patients thought to have BPH should be

examined prior to starting therapy with UROXATRAL (alfuzosin HCl extended-release tablets)
to rule out the presence of carcinoma of the prostate.
Intraoperative Floppy Iris Syndrome (IFIS): IFIS has been observed during cataract surgery
in some patients on or previously treated with alpha-1 blockers. This variant of small pupil
syndrome is characterized by the combination of a flaccid iris that billows in response to
intraoperative irrigation currents, progressive intraoperative miosis despite preoperative dilation
with standard mydriatic drugs, and potential prolapse of the iris toward the phacoemulsification
incisions. The patient’s ophthalmologist should be prepared for possible modifications to their
surgical technique, such as the utilization of iris hooks, iris dilator rings, or viscoelastic
substances.
There does not appear to be a benefit of stopping alpha-1 blocker therapy prior to cataract
surgery.

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Drug-Drug Interactions: The pharmacokinetic and pharmacodynamic interactions between

UROXATRAL and other alpha-blockers have not been determined. However, interactions may
be expected, and UROXATRAL should NOT be used in combination with other alpha-blockers.
Coronary Insufficiency: If symptoms of angina pectoris should newly appear or worsen,
UROXATRAL should be discontinued.
Hepatic Insufficiency: UROXATRAL should not be given to patients with moderate or severe
hepatic insufficiency. (See CONTRAINDICATIONS). The pharmacokinetics of
UROXATRAL have not been studied in patients with mild hepatic insufficiency (See
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Renal Insufficiency: Systemic exposure was increased by approximately 50% in

pharmacokinetic studies of patients with mild, moderate, and severe renal insufficiency (See
CLINICAL PHARMACOLOGY, Special Populations). In phase 3 studies, the safety profile of
patients with mild (n=172) or moderate (n=56) renal impairment was similar to the patients with
normal renal function in those studies. Safety data are available in only a limited number of
patients (n=6) with creatinine clearance below 30 mL/min; therefore, caution should be exercised
when UROXATRAL is administered in patients with severe renal insufficiency.

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Patients with Congenital or Acquired QT Prolongation: In a study of QT effect in 45

healthy males (See CLINICAL PHARMACOLOGY, Electrophysiology), the QT effect
appeared less with alfuzosin 10 mg than with 40 mg, and the effect of alfuzosin 40 mg did not
appear as large as that of the active control moxifloxacin at its therapeutic dose. A post-
marketing study evaluating the effect of combining UROXATRAL with another drug of
comparable QT effect showed an increased effect when compared to either drug alone (see

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CLINICAL PHARMACOLOGY, Electrophysiology). Although this study was not designed to

make direct statistical comparisons between drugs, the QT increase with both drugs was no more
than additive and was lower than that of the active control moxifloxacin. These observations
should be considered in clinical decisions when prescribing UROXATRAL for patients with a
known history of QT prolongation or patients who are taking medications which prolong the QT
interval. There has been no signal of Torsades de Pointe in the extensive post-marketing
experience with alfuzosin. There are no known PK/PD studies of the effects of other alpha-
blockers on cardiac repolarization.

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Information for Patients

Patients should be told about the possible occurrence of symptoms related to postural
hypotension, such as dizziness, when beginning UROXATRAL, and they should be cautioned
about driving, operating machinery, or performing hazardous tasks during this period.
UROXATRAL should be taken with food and with the same meal each day.
Patients should be advised not to crush or chew UROXATRAL tablets.
Laboratory Tests
No laboratory test interactions with UROXATRAL tablets are known.
Pediatric Use
UROXATRAL is not indicated for use in children.

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Geriatric Use

Of the total number of subjects in clinical studies of UROXATRAL, 48% were 65 years of age
and over, whereas 11% were 75 and over. No overall differences in safety or effectiveness were
observed between these subjects and younger subjects. (See CLINICAL PHARMACOLOGY,
Carcinogenesis, Mutagenesis, and Impairment of Fertility
There was no evidence of a drug-related increase in the incidence of tumors in mice following
dietary administration of 100 mg/kg/day alfuzosin for 98 weeks (13 and 15 times the level of
exposure to humans based on AUC of unbound drug) in females and males, respectively. The

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11

highest dose tested in female mice may not have constituted a maximally tolerated dose.
Likewise, there was no evidence of a drug-related increase in the incidence of tumors in rats
following dietary administration of 100 mg/kg/day alfuzosin for 104 weeks (53 and 37 times the
level of exposure to humans based on AUC of unbound drug) in females and males, respectively.
Alfuzosin showed no evidence of mutagenic effect in the Ames and mouse lymphoma assays,
and was free of any clastogenic effects in the Chinese hamster ovary cell and in vivo mouse
micronucleus assays. Alfuzosin treatment did not induce DNA repair in a human cell line.
There was no evidence of reproductive organ toxicity when male rats were given alfuzosin at
daily oral (gavage) doses of up to 250 mg/kg/day for 26 weeks, which corresponds to levels of
exposure several hundred times that in humans. No impairment of fertility was observed
following oral (gavage) administration to male rats at doses of up to 125 mg/kg/day for 70 days.
Estrous cycling was inhibited in rats and dogs at doses of 25 mg/kg and 20 mg/kg, respectively,
corresponding to levels of systemic exposure (based on AUC of unbound drug) 12- and 18-fold
higher, respectively, than in humans, although this did not result in impaired fertility in rats.

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Pregnancy

Teratogenic Effects, Pregnancy and Lactation Category B. UROXATRAL is not indicated
for use in women.
There was no evidence of teratogenicity or embryotoxicity in rats at maternal (oral gavage) doses
up to 250 mg/kg/day, corresponding to systemic exposure levels 1,200-fold higher than in
humans. In rabbits, up to the dose of 100 mg/kg/day (approximately 3 times the clinical dose by
body surface area) given orally (via gavage), no evidence of fetal toxicity or teratogenicity was
seen.
Gestation was slightly prolonged in rats with a maternal dose >5 mg/kg/day (oral gavage), which
corresponds to systemic exposure levels (based on AUC of unbound drug) 12 times higher than
human exposure levels, but there were no difficulties with parturition.
Nursing Mothers
UROXATRAL is not indicated for use in women.
ADVERSE REACTIONS
The incidence of treatment-emergent adverse events has been ascertained from 3 placebo-
controlled clinical trials involving 1,608 men in which daily doses of 10 and 15 mg alfuzosin
were evaluated. In these 3 trials, 473 men received UROXATRAL (alfuzosin HCl 10 mg
extended-release tablets). In these studies, 4% of patients taking UROXATRAL (alfuzosin HCl
extended-release tablets) 10 mg tablets withdrew from the study due to adverse events, compared
with 3% in the placebo group.
Table 4 summarizes the treatment-emergent adverse events that occurred in ≥2% of patients
receiving UROXATRAL, and at an incidence numerically higher than that of the placebo group.
In general, the adverse events seen in long-term use were similar in type and frequency to the
events described below for the 3-month trials.
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Table 4 — Treatment-Emergent Adverse Events Occurring in 2% of UROXATRAL-

Treated Patients and More Frequently than with Placebo in 3-Month Placebo-Controlled
Clinical Studies
Adverse Event
Placebo
UROXATRAL
(n=678)
(n=473)
Dizziness
19 (2.8%)
27 (5.7%)
Upper respiratory tract infection
4 (0.6%)
14 (3.0%)
Headache
12 (1.8%)
14 (3.0%)
Fatigue
12 (1.8%)
13 (2.7%)
The following adverse events, reported by between 1% and 2% of patients receiving
UROXATRAL and occurring more frequently than with placebo, are listed alphabetically by
body system and by decreasing frequency within body system:
Body as a whole: pain
Gastrointestinal system: abdominal pain, dyspepsia, constipation, nausea
Reproductive system: impotence
Respiratory system: bronchitis, sinusitis, pharyngitis
Signs and Symptoms of Orthostasis in Clinical Studies: The adverse events related to
orthostasis that occurred in the double-blind phase 3 studies with alfuzosin 10 mg are
summarized in Table 5. Approximately 20% to 30% of patients in these studies were taking
antihypertensive medication.

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Table 5 — Number (%) of Patients with Symptoms Possibly Associated with Orthostasis in

3-Month Placebo-Controlled Clinical Studies
Symptoms
Placebo
UROXATRAL
(n=678)
(n=473)
Dizziness
19 (2.8%)
27 (5.7%)
Hypotension or postural hypotension
0
2 (0.4%)
Syncope
0
1 (0.2%)
Multiple testing for blood pressure changes or orthostatic hypotension was conducted in the three
controlled studies at each scheduled clinic visit (Days 14, 28, 56, and 84). Patients with a
decrease in systolic blood pressure of >20 mm Hg after 2 minutes standing following being
supine were excluded from the three trials. These tests were considered positive for blood
pressure decrease if (1) supine systolic blood pressure was ≤90 mm Hg, with a decrease ≥20 mm
Hg versus baseline, and/or (2) supine diastolic blood pressure was ≤50 mm Hg, with a decrease
≥15 mm Hg versus baseline. The tests were considered positive for orthostatic hypotension if
there was a decrease in systolic blood pressure of ≥20 mm Hg upon standing from the supine
position during the orthostatic tests. According to these definitions, decreased systolic blood
pressure was observed in none of the 674 placebo patients and 1 (0.2%) of the 469
UROXATRAL patients. Decreased diastolic blood pressure was observed in 3 (0.4%) of the
13
placebo patients and in 4 (0.9%) of the UROXATRAL patients. A positive orthostatic test was
seen in 52 (7.7%) of placebo patients and in 31 (6.6%) of the UROXATRAL patients.
No vital sign measurements were obtained following first dose administration in the phase 3
studies, except for a subset of patients in study 1 who had blood pressure measurements 12 to 16
hours after the first dose to assess the potential to produce orthostatic hypotension. None of
these 35 UROXATRAL treated patients showed a positive test for systolic, diastolic or
orthostatic blood pressure change.
Post-Marketing Adverse Event Reports:

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The following adverse reactions have been identified during post approval use of

UROXATRAL. Because these reactions are reported voluntarily from a population of uncertain
size, it is not always possible to reliably estimate their frequency.
General disorders: edema
Cardiac disorders: tachycardia, chest pain, angina pectoris in patients with pre-existing coronary
artery disease
Gastrointestinal disorders: diarrhea
Hepatobiliary disorders: hepatocellular and cholestatic liver injury (including cases with
jaundice leading to drug discontinuation)
Respiratory system disorders: rhinitis
Reproductive system disorders: priapism
Skin and subcutaneous tissue disorders: rash, pruritis, urticaria, angioedema
Vascular disorders: flushing
During cataract surgery, a variant of small pupil syndrome known as Intraoperative Floppy Iris
Syndrome (IFIS) has been reported in some patients on or previously treated with alpha-1
blockers (see PRECAUTIONS).

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OVERDOSAGE

Should overdose of UROXATRAL (alfuzosin HCl extended-release tablets) lead to hypotension,
support of the cardiovascular system is of first importance. Restoration of blood pressure and
normalization of heart rate may be accomplished by keeping the patient in the supine position. If
this measure is inadequate, then the administration of intravenous fluids should be considered. If
necessary, vasopressors should then be used, and the renal function should be monitored and
supported as needed. Alfuzosin is 82% to 90% proteinbound; therefore, dialysis may not be of
benefit.
DOSAGE AND ADMINISTRATION
The recommended dosage is one 10 mg UROXATRAL (alfuzosin HCl extended-release tablets)
tablet daily to be taken immediately after the same meal each day. The tablets should not be
chewed or crushed.
HOW SUPPLIED
UROXATRAL (alfuzosin HCl extended-release tablets) 10 mg is available as a round, three-
layer tablet: one white layer between two yellow layers, debossed with X10. UROXATRAL is
supplied as follows:
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Package

NDC Number
Bottles of 30
0024-4200-30
Bottles of 100
0024-4200-10
Hospital Unit Dose (blister packs containing 10 cards of 10 tablets each)
0024-4200-20
Rx only.
Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled
Room Temperature].
Protect from light and moisture.
Keep UROXATRAL out of reach of children.
sanofi-aventis U.S. LLC
Bridgewater, NJ 08807
UROXATRAL
®
is a registered trademark of sanofi-aventis U.S. LLC.
Revised August 2008
15

Patient Information

 

UROXATRAL®

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(Alfuzosin hydrochloride
extended-release tablets)
Read the Patient Information that comes with UROXATRAL before you start using it and each
time you get a refill. There may be new information. This leaflet does not take the place of
talking with your doctor about your condition or your treatment. You and your doctor should
talk about all your medicines, including UROXATRAL, now and at your regular checkups.
What is the most important information I should know about UROXATRAL?

 

UROXATRAL can cause:

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a sudden drop in blood pressure, especially when you start treatment. This may lead to
fainting, dizziness, or lightheadedness. Do not drive, operate machinery, or do any
dangerous activities until you know how UROXATRAL affects you. This is especially
important if you already have a problem with low blood pressure or take medicines to
treat high blood pressure. If you begin to feel dizzy or lightheaded, lie down with your
legs and feet up, and if your symptoms do not improve call your doctor.
What is UROXATRAL?
UROXATRAL is a prescription medicine that is called an “alpha-blocker”. UROXATRAL is
used in adult men to treat the symptoms of benign prostatic hyperplasia (BPH). UROXATRAL
may help to relax the muscles in the prostate and the bladder which may lessen the symptoms of
BPH and improve urine flow.

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Before prescribing UROXATRAL, your doctor may examine your prostate gland and do a blood

test called a prostate specific antigen (PSA) test to check for prostate cancer. Prostate cancer and
BPH can cause the same symptoms. Prostate cancer needs a different treatment.

 

UROXATRAL is not for use in women or children.

Some medicines called “alpha-blockers” are used to treat high blood pressure. UROXATRAL
has not been studied for the treatment of high blood pressure.
Who should not take UROXATRAL?

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Do not take UROXATRAL if you:

• have liver problems
• are taking antifungal drugs like ketoconazole or HIV drugs called protease inhibitors
• are already taking an alpha-blocker for either high blood pressure or prostate problems
16
• are a woman
• are a child under the age of 18
• are allergic to UROXATRAL. The active ingredient is alfuzosin hydrochloride. See the
end of this leaflet for a complete list of ingredients in UROXATRAL.

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Before taking UROXATRAL, tell your doctor:

• if you have liver problems
• if you have kidney problems
• if you or any family members have a rare heart condition known as congenital prolongation
of the QT interval.
• about all the medicines you take, including prescription and non-prescription medicines,
vitamins and herbal supplements. Some of your other medicines may affect the way you
respond or react to UROXATRAL.
• if you have had low blood pressure, especially after taking another medicine. Signs of low
blood pressure are fainting, dizziness, and lightheadedness.
• if you have a heart problem called angina (pain in your chest, jaw, or arm).
What you need to know while taking UROXATRAL (alfuzosin HCl) tablets
• If you have an eye surgery for cataract (clouding of the eye) planned, tell your
ophthalmologist that you are using UROXATRAL or have previously been treated with an
alpha-blocker.
How do I take UROXATRAL?
• Take UROXATRAL exactly as your doctor prescribes it.
• Take one UROXATRAL tablet after the same meal each day. UROXATRAL should be
taken just after eating food. Do not take it on an empty stomach.
• Swallow the UROXATRAL tablet whole. Do not crush, split, or chew UROXATRAL
tablets.
• If you take too much UROXATRAL call your local poison control center or emergency
room right away.
17
What are the possible side effects of UROXATRAL?
The most common side effects with UROXATRAL are:
• dizziness
• headache
• tiredness
Call your doctor if you get any side effect that bothers you.
These are not all the side effects of UROXATRAL. For more information ask your doctor or
pharmacist.

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How do I store UROXATRAL?

Store UROXATRAL between 59°F and 86°F (15°C and 30°C).
Protect from light and moisture.
Keep UROXATRAL and all medicines out of the reach of children.
General information about UROXATRAL:
Medicines are sometimes prescribed for conditions that are not mentioned in patient information
leaflets. Do not use UROXATRAL for a condition for which it was not prescribed. Do not give
UROXATRAL to other people, even if they have the same symptoms you have. It may harm
them.
This leaflet summarizes the most important information about UROXATRAL. If you would like
more information, talk with your doctor. You can ask your doctor or pharmacist for information
about UROXATRAL that is written for health professionals.
You may also visit our website at www.UROXATRAL.com or call 1-800-446-6267.

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What are the ingredients of UROXATRAL?

Active Ingredient: alfuzosin hydrochloride
Inactive Ingredients: colloidal silicon dioxide (NF), ethylcellulose (NF), hydrogenated castor
oil (NF), hydroxypropyl methylcellulose (USP), magnesium stearate (NF), mannitol (USP),
microcrystalline cellulose (NF), povidone (USP), and yellow ferric oxide (NF).
Rev. August 2008
18
Rx Only
UROXATRAL
®
is a registered trademark of sanofi-aventis U.S. LLC.
sanofi-aventis U.S. LLC
Bridgewater, NJ 08807

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19

 

 

 

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2.3

Barrier Therapeutics Receives FDA Approval for Solage(R) Topical Solution Labeling Expansion

Posted on: Thursday, 3 May 2007, 12:00 CDT

Source

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Barrier Therapeutics, Inc. (NASDAQ: BTRX), a pharmaceutical company that develops and markets dermatology products, today announced that the U.S. Food and Drug Administration (FDA) approved the company's application to add clinical data to the prescribing information for Solage(R) (mequinol 2%, tretinoin 0.01%) Topical Solution. The newly added information shows that Solage treatment for solar lentigines (age spots) is safe and effective in patients with darker skin types.

The new prescribing information includes data from a Phase 4 post-approval study that demonstrated favorable results on the efficacy, safety and tolerability of Solage for the treatment of solar lentigines in patients with darker skin types. Study findings on the safety and tolerability of Solage in darker phototypes demonstrated a favorable benefit-to-risk ratio in the treatment of solar lentigines in African American, Asian and Latin/Hispanic patients. Over 80% of treated patients in this study achieved a significant response to therapy for facial and arm lesions. Additionally, the majority of subjects maintained clinical benefit during a 4-week post treatment period. These results are consistent with efficacy findings previously reported for Caucasian individuals.

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Ingredients and technical source:

Pharmacology and use:


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Tretinoin, also known as all-trans-retinoic acid (ATRA), is a naturally occurring derivative of vitamin A (retinol). Retinoids such as tretinoin are important regulators of cell reproduction, proliferation, and differentiation and are used to treat acne and photodamaged skin and to manage keratinization disorders such as ichthyosis and keratosis follicularis.

Tretinoin also represents the class of anticancer drugs called differentiating agents and is used in the treatment of acute promyelocytic leukemia (APL).

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For the the induction of remission in patients with acute promyelocytic leukemia (APL), French-American-British (FAB) classification M3 (including the M3 variant); For the topical treatment of acne vulgaris, flat warts and other skin conditions (psoriasis, ichthyosis congenita, icthyosis vulgaris, lamellar icthyosis, keratosis palmaris et plantaris, epidermolytic hyperkeratosis, senile comedones, senile keratosis, keratosis follicularis (Darier's disease),

and basal cell carcinomas.);

For palliative therapy to improve fine wrinkling, mottled hyperpigmentation, roughness associated with photodamage.

Mechanism Of Action:

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Tretinoin binds to alpha, beta, and gamma retinoic acid receptors (RARs). RAR-alpha and RAR-beta have been associated with the development of acute promyelocytic leukemia and squamous cell cancers, respectively. RAR-gamma is associated with retinoid effects on mucocutaneous tissues and bone.

Although the exact mechanism of action of tretinoin is unknown, current evidence suggests that the effectiveness of tretinoin in acne is due primarily to its ability to modify abnormal follicular keratinization. Comedones form in follicles with an excess of keratinized epithelial cells.

Tretinoin promotes detachment of cornified cells and the enhanced shedding of corneocytes from the follicle. By increasing the mitotic activity of follicular epithelia, tretinoin also increases the turnover rate of thin, loosely-adherent corneocytes. Through these actions, the comedo contents are extruded and the formation of the microcomedo, the precursor lesion of acne vulgaris, is reduced. Tretinoin is not a cytolytic agent but instead induces cytodifferentiation and decreased proliferation of APL cells in culture and in vivo. When Tretinoin is given systemically to APL patients, tretinoin treatment produces an initial maturation of the primitive promyelocytes derived from the leukemic clone, followed by a repopulation of the bone marrow and peripheral blood by normal, polyclonal hematopoietic cells in patients achieving complete remission (CR). The exact mechanism of action of tretinoin in APL is unknown.

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Manufacturer:
No Manufacturer Listed

Description

Source of This Canadian Data:
Solagé Solution is the first combination topical product approved for the treatment of solar lentigines (age/sun spots) in conjunction with a comprehensive skin care and sun avoidance program.

Solagé Solution is quick drying and has a unique contoured felt tip delivery system that allows for targeted application. It is a quick-drying solution for easy twice-daily use.

Directions
Solagé Solution is to be used twice daily, at least eight hours apart, or as directed by your doctor. It is a drug for topical use only and is not a cosmetic preparation. Do not use Solagé Solution around your eyes, lips, creases of the nose or mucous membranes. Solagé Solution may cause severe redness, itching, burning, stinging, and peeling if applied to these areas. If the product gets in your eyes, rinse thoroughly with water and contact your doctor.

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Apply Solagé Solution to the age spots using the applicator provided with the medication. Avoid application of Solagé Solution to the surrounding, normally colored skin. Only enough Solagé Solution should be applied to make the lesion appear moist – running or dripping of the medication should be avoided. Applications of larger amounts of Solagé Solution, or more frequent applications than recommended, will not lead to more rapid or better results, and marked redness, peeling, irritation or hypopigmentation may occur. You should not shower or bathe the treatment areas for at least 6 hours after application of Solagé Solution.

Stop treating any age spots that become the same color or lighter than your normally colored skin. If the skin surrounding an age spot becomes lighter than your normally colored skin, stop treating that age spot and contact your doctor regarding continued use of Solagé Solution to that age spot.

If you forget or miss a dose of Solagé Solution, do not try to "make it up." Return to your normal application schedule as soon as you can.

If sensitivity or increased irritation occurs, stop use of Solagé Solution and contact your doctor.

If the age spots become darker with treatment, stop use of Solagé Solution and contact your doctor.

Do not use Solagé Solution for any condition other than for which it was prescribed by your doctor. Do not give it to other persons or allow other persons to use it.

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You may use cosmetics after applying Solagé Solution but you should wait 30 minutes before applying.

Cautions

Solagé Solution may cause redness, stinging, burning or irritation on areas of the skin where it is applied. It may also cause peeling and itching of the areas where applied. Excessive or prolonged application of Solagé Solution may cause the treated age spots or surrounding skin to become temporarily lighter than your normally colored skin. Discontinue application of Solagé Solution to any such affected areas. What should I avoid while using Solagé Solution? Solagé Solution increases your sensitivity to sunlight. Sun exposure (natural or artificial) to areas of the skin treated with Solagé Solution should be avoided. Wear protective clothing if exposure to the sun cannot be avoided. Patients using Solagé Solution should practice a comprehensive sun protection program. Following discontinuation of Solagé Solution, patients should continue to practice a comprehensive sun protection program. Solagé Solution should be used with caution if you are also using other topical products with a strong drying effect on the skin, products with high concentrations of alcohol, astringents, spices or lime, medicated soaps, or shampoos, permanent wave solutions, electrolysis, hair removal products or waxes, or other preparations or processes that may dry or irritate your skin. If you are using any of these types of products, tell your doctor before using Solagé Solution.

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3.2

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PSA Test Official Government Data

Prostate-Specific Antigen (PSA) Test

Top Of This Segment - PSA

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Source

Karl Note: The original text includes a great many links which do not work on this page. I have left those links here, for your possible use. If you want to use all the links, simply go to the source page, link above. If you click on the links, other than the links to THE QUESTION LINKS, you will get non-useful results.

The links to the question are working here. I've made them larger than the original and they are in purple color.

Return To Top Of Segment

Key Points
  • Prostate-specific antigen (PSA) is a protein produced by cells of the prostate gland. The PSA test measures the level of PSA in the blood (see Question 1).
  • The U.S. Food and Drug Administration (FDA) has approved the use of the PSA test along with a digital rectal exam to help detect prostate cancer in men age 50 and older. The FDA has also approved the PSA test to monitor patients with a history of prostate cancer to see if the cancer has recurred (come back) (see Question 2).

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  • Doctors’ recommendations for PSA screening vary (see Question 3).
  • The higher a man’s PSA level, the more likely it is that cancer is present, but there are other possible reasons for an elevated PSA level (see Questions 4 and 5).
  • Doctors take several factors into account for men who have a rising PSA level after treatment for prostate cancer (see Questions 2 and 6).
  • The PSA test for screening has limitations and is still controversial (see Questions 7 and 8).
  • Researchers are studying ways to validate and improve the PSA test and to find other ways of detecting prostate cancer early (see Questions 9 and 10).
  1. What is the prostate-specific antigen (PSA) test?

    Return To Top Of Segment

    Prostate-specific antigen (PSA) is a protein produced by cells of the prostate gland. The PSA test measures the level of PSA in the blood. The doctor takes a blood sample, and the amount of PSA is measured in a laboratory. Because PSA is produced by the body and can be used to detect disease, it is sometimes called a biological marker or a tumor marker.

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

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    It is normal for men to have a low level of PSA in their blood; however, prostate cancer or benign (not cancerous) conditions can increase a man’s PSA level. As men age, both benign prostate conditions and prostate cancer become more common. The most frequent benign prostate conditions are prostatitis (inflammation of the prostate) and benign prostatic hyperplasia (BPH) (enlargement of the prostate). There is no evidence that prostatitis or BPH causes cancer, but it is possible for a man to have one or both of these conditions and to develop prostate cancer as well.

    A man’s PSA level alone does not give doctors enough information to distinguish between benign prostate conditions and cancer. However, the doctor will take the result of the PSA test into account when deciding whether to check further for signs of prostate cancer.

  2. Why is the PSA test performed?

    Return To Top Of Segment

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    The U.S. Food and Drug Administration (FDA) has approved the use of the PSA test along with a digital rectal exam (DRE) to help detect prostate cancer in men 50 years of age or older. During a DRE, a doctor inserts a gloved finger into the rectum and feels the prostate gland through the rectal wall to check for bumps or abnormal areas. Doctors often use the PSA test and DRE as prostate cancer screening tests; together, these tests can help doctors detect prostate cancer in men who have no symptoms of the disease.

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    The FDA has also approved the use of the PSA test to monitor patients who have a history of prostate cancer to see if the cancer has recurred (come back). If a man’s PSA level begins to rise, it may be the first sign of recurrence. Such a “biochemical relapse” typically precedes clinical signs and symptoms of a relapse by months or years. However, a single elevated PSA measurement in a patient with a history of prostate cancer does not always mean the cancer has come back. A man who has been treated for prostate cancer should discuss an elevated PSA level with his doctor. The doctor may recommend repeating the PSA test or performing other tests to check for evidence of a recurrence. The doctor may look for a trend of rising PSA measurements over time rather than a single elevated PSA level.

    It is important to note that a man who is receiving hormone therapy for prostate cancer may have a low PSA level during, or immediately after, treatment. The low level may not be a true measure of the man’s PSA level. Men receiving hormone therapy should talk with their doctor, who may advise them to wait a few months after hormone treatment before having a PSA test.

  3. For whom might a PSA screening test be recommended?

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    Return To Top Of Segment

    Doctors’ recommendations for screening vary. Some encourage yearly screening for men over age 50, and some advise men who are at a higher risk for prostate cancer to begin screening at age 40 or 45. Others caution against routine screening. Although specific recommendations regarding PSA screening vary, there is general agreement that men should be informed about the potential risks and benefits of PSA screening before being tested. Currently, Medicare provides coverage for an annual PSA test for all men age 50 and older.

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    Several risk factors increase a man’s chances of developing prostate cancer. These factors may be taken into consideration when a doctor recommends screening. Age is the most common risk factor, with nearly 63 percent of prostate cancer cases occurring in men age 65 and older (1). Other risk factors for prostate cancer include family history, race, and possibly diet. Men who have a father or brother with prostate cancer have a greater chance of developing prostate cancer. African American men have the highest rate of prostate cancer, while Asian and Native American men have the lowest rates. In addition, there is some evidence that a diet higher in fat, especially animal fat, may increase the risk of prostate cancer.
  4. How are PSA test results reported?

    Return To Top Of Segment

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    PSA test results show the level of PSA detected in the blood. These results are usually reported as nanograms of PSA per milliliter (ng/mL) of blood. In the past, most doctors considered a PSA level below 4.0 ng/mL as normal. In one large study, however, prostate cancer was diagnosed in 15.2 percent of men with a PSA level at or below 4.0 ng/mL (2). Fifteen percent of these men, or approximately 2.3 percent overall, had high-grade cancers (2). In another study, 25 to 35 percent of men who had a PSA level between 4.1 and 9.9 ng/mL and who underwent a prostate biopsy were found to have prostate cancer, meaning that 65 to 75 percent of the remaining men did not have prostate cancer (3).

    Thus, there is no specific normal or abnormal PSA level. In addition, various factors, such as inflammation (e.g., prostatitis), can cause a man’s PSA level to fluctuate. It is also common for PSA values to vary somewhat from laboratory to laboratory. Consequently, one abnormal PSA test result does not necessarily indicate the need for a prostate biopsy. In general, however, the higher a man’s PSA level, the more likely it is that cancer is present. Furthermore, if a man’s PSA level continues to rise over time, other tests may be needed.

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    Because PSA levels tend to increase with age, the use of age-specific PSA reference ranges has been suggested as a way of increasing the accuracy of PSA tests. However, age-specific reference ranges have not been generally favored because their use may lead to missing or delaying the detection of prostate cancer in as many as 20 percent of men in their 60s and 60 percent of men in their 70s. Another complicating factor is that studies to establish the normal range of PSA values have been conducted primarily in white men. Although expert opinions vary, there is no clear consensus on the optimal PSA threshold for recommending a prostate biopsy for men of any racial or ethnic group.

  5. What if the screening test results show an elevated PSA level?

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    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    A man should discuss an elevated PSA test result with his doctor. There can be different reasons for an elevated PSA level, including prostate cancer, benign prostate enlargement, inflammation, infection, age, and race.

    If no symptoms to suggest cancer are present, the doctor may recommend repeating DRE and PSA tests regularly to watch for any changes. If a man’s PSA level has been increasing or if a suspicious lump is detected during a DRE, the doctor may recommend other tests to determine if there is cancer or another problem in the prostate. A urine test may be used to detect a urinary tract infection or blood in the urine. The doctor may recommend imaging tests, such as a transrectal ultrasound (a test in which high-frequency sound waves are used to obtain images of the rectum and nearby structures, including the prostate), x-rays, or cystoscopy (a procedure in which a doctor looks into the urethra and the bladder through a thin, lighted tube that is inserted through the end of the penis; this can help determine whether urinary blockage is caused by an enlarged prostate). Medicine or surgery may be recommended if the problem is BPH or an infection.

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    If cancer is suspected, a biopsy is needed to determine whether cancer is present in the prostate. During a biopsy, samples of prostate tissue are removed, usually with a needle, and viewed under a microscope. The doctor may use ultrasound to view the prostate during the biopsy, but ultrasound cannot be used alone to tell if cancer is present.

  6. What if the test results show a rising PSA level after treatment for prostate cancer?

    Return To Top Of Segment

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    A man should discuss rising PSA test results with his doctor. Doctors consider a number of factors before recommending further treatment. Additional treatment based on a single PSA test result is often not recommended. Rather, a rising trend in PSA test results over a period of time combined with other findings, such as an abnormal DRE, positive prostate biopsy results, or abnormal CT (computed tomography) scan results, may lead to a recommendation for further treatment.

    According to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines in Oncology for Prostate Cancer (4), additional treatment may be indicated based on the following PSA test results:

    • For men who have been in the watchful waiting phase—their PSA level has doubled in fewer than 3 years or they have a PSA velocity (change in PSA level over time) of greater than 0.75 ng/mL per year, or they have a prostate biopsy showing evidence of worsening cancer (4).
    • For men who have had a radical prostatectomy (removal of the prostate gland)—their PSA level does not fall below the limits of detection after surgery or they have a detectable PSA level (> 0.3 ng/mL) that increases on two or more subsequent measurements after having no detectable PSA (4).
    • For men who have had other initial therapy, such as radiation therapy with or without hormonal therapy—their PSA level has risen by 2 ng/mL or more after having no detectable PSA or a very low PSA level (4).

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    Please note that these are general guidelines. Prostate cancer is a complex disease and many variables need to be considered by each patient and his doctor.

  7. What are some of the limitations of the PSA test?

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      Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

      Detecting tumors does not always mean saving lives: When used in screening, the PSA test can detect small tumors. However, finding a small tumor does not necessarily reduce a man's chances of dying from prostate cancer. PSA testing may identify very slow-growing tumors that are unlikely to threaten a man's life. Also, PSA testing may not help a man with a fast-growing or aggressive cancer that has already spread to other parts of his body before being detected.
    • False-positive tests: False-positive test results (also called false positives) occur when the PSA level is elevated but no cancer is actually present. False positives may lead to additional medical procedures that have potential risks and significant financial costs and can create anxiety for the patient and his family. Most men with an elevated PSA test result turn out not to have cancer; only 25 to 35 percent of men who have a biopsy due to an elevated PSA level actually have prostate cancer (3).
    • False-negative tests: False-negative test results (also called false negatives) occur when the PSA level is in the normal range even though prostate cancer is actually present. Most prostate cancers are slow-growing and may exist for decades before they are large enough to cause symptoms. Subsequent PSA tests may indicate a problem before the disease progresses significantly.

  8. Why is the PSA test controversial in screening?

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    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    Using the PSA test to screen men for prostate cancer is controversial because it is not yet known for certain whether this test actually saves lives. Moreover, it is not clear that the benefits of PSA screening outweigh the risks of follow-up diagnostic tests and cancer treatments. For example, the PSA test may detect small cancers that would never become life threatening. This situation, called overdiagnosis, puts men at risk of complications from unnecessary treatment.

  9. The procedure used to diagnose prostate cancer (prostate biopsy) may cause harmful side effects, including bleeding and infection. Prostate cancer treatments, such as surgery and radiation therapy, may cause incontinence (inability to control urine flow), erectile dysfunction (erections inadequate for intercourse), and other complications. For these reasons, it is important that the benefits and risks of diagnostic procedures and treatment be taken into account when considering whether to undertake prostate cancer screening.

  10. Question #9 - What research is being done to validate and improve the PSA test?

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    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    The benefits of screening for prostate cancer are still being studied. The National Cancer Institute (NCI), a component of the National Institutes of Health, is currently conducting the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial, or PLCO trial, to determine whether certain screening tests can help reduce the number of deaths from these cancers. The PSA test and DRE are being evaluated to determine whether yearly screening to detect prostate cancer will decrease a man’s chances of dying from this disease.

    Initial results from the trial showed that annual PSA testing for 6 years and annual DRE testing for 4 years (performed in the same years as the first four PSA tests) did not reduce the number of deaths from prostate cancer through a median follow-up period of 11.5 years (range 7.2 to 14.8 years) (5). At 7 years of follow-up, a point in time when follow-up of the participants was essentially complete, 23 percent more cancers had been diagnosed in the screening group than in the control group. In the control group, men were randomly assigned to “usual care.”

    These results suggest that many men were diagnosed with, and treated for, cancers that would not have been detected in their lifetime without screening and, as a consequence, were exposed to the potential harms of unnecessary treatments, such as surgery and radiation therapy. Nevertheless, it remains possible that a small benefit from the earlier detection of these “excess” cancers could emerge with longer follow-up. Follow-up of the PLCO participants will continue, therefore, until all participants have been followed for at least 13 years.

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  11. Not a Question here. Return To Top Of Segment

    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    In contrast, initial results from another large randomized, controlled trial of prostate cancer screening, called the European Randomized Study of Screening for Prostate Cancer (ERSPC), found a 20 percent reduction in prostate cancer deaths associated with PSA testing every 4 years (6). At the time the results were reported, the participants had been followed for a median of 9 years. The average number of PSA tests per participant in ERSPC was 2.1. Most participating centers in this study used a lower PSA cutoff value as an indicator of abnormality than was used in the PLCO trial (3.0 ng/mL versus 4.0 ng/mL). As in the PLCO trial, many more cancers were diagnosed in the screening group than in the control group. The ERSPC researchers estimated that 1,410 men would have to be screened and 48 additional cancers would have to be detected to prevent one death from prostate cancer (6).

  12. Scientists are also researching ways to improve the PSA test, hopefully to allow cancerous and benign conditions, as well as slow-growing cancers and fast-growing, potentially lethal cancers, to be distinguished from one another. Some of the methods being studied include the following:

    • PSA velocity: PSA velocity is the change in PSA level over time. A sharp rise in the PSA level raises the suspicion of cancer and may indicate a fast-growing cancer. A 2006 study found that men who had a PSA velocity above 0.35 ng/mL per year had a higher relative risk of dying from prostate cancer than men who had a PSA velocity less than 0.35 ng/mL per year (7). More studies are needed to determine if a high PSA velocity more accurately detects prostate cancer early.
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    • PSA density: PSA density considers the relationship between the level of PSA and the size of the prostate. In other words, an elevated PSA level might not arouse suspicion if a man has a very enlarged prostate. The use of PSA density to interpret PSA results is controversial because cancer might be overlooked in a man with an enlarged prostate.
    • Free versus attached PSA: PSA circulates in the blood in two forms: Free or attached to a protein molecule. The free PSA test is more often used for men who have higher PSA values. Free PSA may help tell what kind of prostate problem a man has. With benign prostate conditions (such as BPH), there is more free PSA, while cancer produces more of the attached form. If a man’s attached PSA level is high but his free PSA level is not, the presence of cancer is more likely. In this case, more testing, such as a prostate biopsy, may be done. Researchers are exploring additional ways of measuring PSA and comparing these measurements to determine whether cancer is present.
    • Alteration of PSA cutoff level: Some researchers have suggested lowering the cutoff levels used to determine whether a PSA measurement is normal or elevated. For example, a number of studies have used cutoff levels of 2.5 or 3.0 ng/mL (rather than 4.0 ng/mL). In such studies, PSA measurements above 2.5 or 3.0 ng/mL are considered elevated. Researchers hope that using these lower cutoff levels will increase the chance of detecting prostate cancer; however, this method may also increase overdiagnosis and false-positive test results and lead to unnecessary medical procedures. (See ERSPC trial results above.)

  13. Question #10

    What other methods are being studied to detect prostate cancer?


    Karl Note: Note that the PSA MAY be only a marker for an enlarged prostate gland, with no existing cancer. This is a modern finding, not much reflected in this government resource.

    Return To Top Of Segment

    Researchers are investigating several other ways to detect prostate cancer that could be used alone or together with the PSA test and DRE. Some of these include the following:

    • MicroRNA patterns: MicroRNAs are small, single-strand molecules of ribonucleic acid (RNA) that regulate important cellular functions. Researchers have found that the pattern of microRNAs in a cell can differ depending on the type of cell and between healthy cells and abnormal cells, such as cancer cells. Some research also suggests that the microRNA patterns in early-stage prostate cancer and late-stage prostate cancer may be different.
    • Non-mutation gene alterations: The activity of a gene can be altered in ways that do not involve a change (mutation) to its DNA code. This can occur by modifying the gene’s DNA through a process known as methylation or by modifying the proteins that bind to the gene and help control how it is configured in the chromosome on which it is located. These types of gene alterations are called epigenetic alterations. Research has already shown that certain genes become hypermethylated and inactivated during the development and progression of prostate cancer. Scientists hope to identify DNA methylation changes and protein modifications that will be able to identify prostate cancer early and help predict tumor behavior.
    • Gene fusions: Sometimes genes on different chromosomes can come together inappropriately and fuse to form hybrid genes. These hybrid genes have been found in several types of cancer, including prostate cancer, and may play a role in cancer development. The gene fusions found in prostate cancer involve members of the ETS family of oncogenes, which are genes that cause cancer when mutated or expressed at higher than normal levels. Researchers are investigating whether diagnostic or prognostic tests based on gene fusions can be developed.
    • PCA3: PCA3, also known as DD3, is a prostate-specific RNA that is reported to be expressed at high levels in prostate tumor cells. It does not appear to contain the genetic code for a protein. A urine test for this RNA, to be used in addition to current prostate cancer screening tests, has the potential to be useful and is under study.
    • Differential detection of metabolites: Molecules produced by the body’s metabolic processes, or metabolites, may be able to help distinguish between benign prostate tissue, localized prostate cancer, and metastatic prostate cancer. One such molecule, known as sarcosine, has been identified and may be associated with prostate cancer’s invasiveness and aggressiveness. Ongoing research is investigating whether a test based on sarcosine can be developed.
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    • Proteo-imaging: Proteo-imaging is the ability to localize and follow changes at the molecular level, through imaging, of the protein distributions in specific tissues. Being able to see different patterns of protein expression in healthy prostate tissue versus abnormal prostate tissue may help classify early prostate changes that may one day lead to cancer.
    • Protein patterns in the blood: Researchers are also studying patterns of proteins in the blood to see if they can identify one or more unique patterns that indicate the presence of prostate cancer and allow more aggressive cancers to be distinguished from less aggressive ones.

Selected References

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  1. Ries LAG, Melbert D, Krapcho M, et al. SEER Cancer Statistics Review, 1975–2005. Bethesda, MD: National Cancer Institute, 2008. Available online at http://seer.cancer.gov/csr/1975_2005/index.html on the Internet. Last accessed March 18, 2009.
  2. Thompson IM, Pauler DK, Goodman PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level < or = 4.0 ng per milliliter. New England Journal of Medicine 2004; 350(22):2239–2246.
  3. Smith DS, Humphrey PA, Catalona WJ. The early detection of prostate carcinoma with prostate specific antigen: The Washington University experience. Cancer 1997; 80(9):1853–1856.
  4. National Comprehensive Cancer Network (2009). NCCN Clinical Practice Guidelines in Oncology™: Prostate Cancer v.2.2009. Retrieved March 18, 2009, from http://www.nccn.org/professionals/physician_gls/PDF/prostate.pdf.
  5. Andriole G, Crawford E, Grubb R, et al. Seven year mortality results and related findings from the prostate component of the PLCO randomized cancer screening trial. New England Journal of Medicine. Published online ahead of print March 18, 2009.
  6. Schröder FH, Hugosson J, Roobol MJ, et al. Screening and prostate-cancer mortality in a randomized European study. New England Journal of Medicine 2009; 360(13):1320–1328.
  7. Carter HB, Ferrucci L, Kettermann A, et al. Detection of life-threatening prostate cancer with prostate-specific antigen velocity during a window of curability. Journal of the National Cancer Institute 2006; 98(21):1521–1527.
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3.2

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Official FDA Description of this Prostate Health Problem

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Source quoted from FDA Source

About Enlarged Prostate

Enlarged prostate is a prevalent and progressive disease that affects 50 percent of men over 50 years of age and over 90 percent of men older than age 80.1 An enlarged prostate causes changes in urinary habits because of its location around the urethra. Over time, the prostate can continue to grow and urinary symptoms may worsen as the bladder loses the ability to empty itself. Left untreated, in severe cases, an enlarged prostate can lead to serious long-term problems including acute urinary retention (AUR) and the need for prostate-related surgery, and in rare cases even kidney or bladder damage.

3.3

Prostate Cancer Treatment Choices

Source

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Congress has not been willing to change the basic economics of health care nor is it interested in changing how medicine is practiced in the United States. No matter how wrong, expensive, ineffective and dangerous Congress refuses to go to the roots of the crisis and make necessary changes. Fixing the fundamental problem with our medical system (soaring costs and mediocre results) requires that we look much deeper at the problem. If we don’t, the medical system will remain deeply troubled and will continue to hurt more people than it helps.

Prostate cancer is a case in point. The official story about prostate cancer is that men can choose from at least five different courses of treatment. The simplest is known as

watchful waiting,

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which means doing nothing unless later tests show the cancer is worsening. More aggressive options include removing the prostate gland or receiving one of several forms of radiation. The latest treatment called proton radiation therapy involves a proton accelerator that can be as big as a football field with the treatments costing 100,000. Unfortunately for the developers and investors very few people will be able to afford that option with a cataclysmic economic collapse in the making.

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Prostate cancer kills an estimated 35,000 men in the United States each year and attacks another 165,000. Most cases of prostate cancer do not occur until after men turn 50, but in recent years there has been a steady rise in the percentage of men in their 30s and 40s with both prostate problems and prostate cancer, primarily as a result of poor diet and increasing environmental pollution. One man in six will get prostate cancer during his lifetime

The New York Times reported that, “Some doctors swear by one treatment, others by another. But no one really knows which is best. Rigorous research has been scant. Above all, no serious study has found that the high-technology treatments do better at keeping men healthy and alive. Most die of something else before prostate cancer becomes a problem.” “No therapy has been shown superior to another,” an analysis by the RAND Corporation found. Dr. Michael Rawlins, the chairman of a British medical research institute, said  “We’re not sure how good any of these treatments are.” When asked, Dr. Daniella Perlroth of Stanford University, who has studied the data, what she would recommend to a family member, she paused. Then she said, “Watchful waiting.”

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1) Watchful waiting costs a few thousand dollars in doctor visits and tests. Actually watching and waiting means doing nothing when there are plenty of wonderful and natural things one can do to improve PSA scores. (Note below that PSA scores do not offer the best guidance.)
2) Surgery to remove the prostate gland costs about $23,000; possible complications include impotence and urinary incontinence.
3) A targeted form of radiation, known as I.M.R.T., runs $50,000. I.M.R.T. involves a large time commitment, requiring patients to visit a radiation center 45 times over the course of nine weeks. A concern that the multiple-beam radiation of I.M.R.T. may raise the risk of secondary cancers since science already knows that radiation exposure causes cancer.

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4) Proton radiation therapy often exceeds $100,000.

Use of I.M.R.T. rose tenfold from 2002 to 2006, according to RAND data. A new proton treatment center will open in July of 2009 in Oklahoma City, and others are being planned in Chicago, South Florida and elsewhere. The NY Times is very clear about the high costs of this procedure saying, “You may never see this bill, but you’re paying it. It has raised your health insurance premiums and left your employer with less money to give you a decent raise. The cost of prostate cancer care is one small reason that some companies have stopped offering health insurance. It is also one reason that medical costs are on a pace to make the federal government insolvent.

The cause of prostate cancer is unknown medical officials say
 but that is really not true. There are many known causes and
 profiles that help guide our treatment and necessary changes of life.

A report published in the June, 2009 issue of A Cancer Journal for Clinicians shows that routine PSA blood tests often result in over diagnosis of prostate cancer, resulting in unnecessary treatments and psychosocial harm. Drs. Boyle and Brawley, of the International Prevention Research Institute, Lyon, France said, "The real impact and tragedy of prostate cancer screening is the doubling of the lifetime risk of a diagnosis of prostate cancer with little if any decrease in the risk of dying from this disease." 1

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The PSA era is over in the United States," says Dr. Thomas Stamey, professor of urology and lead author of a study published in the Journal of Urology. "Our study raises a very serious question of whether a man should even use the PSA test for prostate cancer screening any more.2 From the time it first became standard to remove prostates in response to high PSA levels to the present - reveals that as a screen, the test now indicates nothing more than the size of the prostate gland.”3

According to the American Cancer Society, “There can be different reasons for an elevated PSA level, including prostate cancer, benign prostate enlargement, inflammation, infection, age, and race,” all factors that make PSA test results confusing, leading to potential for unnecessary treatment and suffering when tests are elevated.

Complications of ill advised prostate cancer treatments include
urinary incontinence and erectile dysfunction, both difficult
 to reverse and both significantly decreasing the quality of life.

The Times did not mention the option of doing what makes sense while one watches and waits and it is hard to understand why. There is a list of natural nutritional agents that are helpful in treating prostate cancer including getting lots of sun exposure to drive up Vitamin D levels, which costs virtually nothing to do.  One might need to purchase full spectrum sun lamps if one lives at extreme latitudes or if the sun is not shining enough but even that option is not costly. Iodine is also a key component because reduced iodine levels in the breasts, ovaries, thyroid and prostate glands predispose one to higher cancer risk.

The great advantage of knowing the prime cause of a disease is
 that it can then be attacked logically and over a broad front.
                                                                                    Dr. Otto Warburg

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Prostate cancer is cancer that grows in prostate gland.
The prostate is a small, walnut-sized structure that makes
 up part of a man's reproductive system. It wraps around
the urethra, the tube that carries urine out of the body.

Iodine as Chemo Agent

Dr. David Derry said, “Lugol's solution is an iodine-in-water solution used by the medical profession for 200 years. One drop (6.5 mg per drop) of Lugol's daily in water, orange juice or milk will gradually eliminate the first phase of the cancer development namely fibrocystic disease of the breast so no new cancers can start. It also will kill abnormal cells floating around in the body at remote sites from the original cancer. Of course this approach appears to work for prostate cancer as prostate cancer is similar to breast cancer in many respects. Indeed, it likely will help with most cancers.”

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There are over 1 million prostate cancer tissue biopsy procedures performed annually in the U.S. Approximately 25% of these tissue biopsies are reported “positive”, indicating the presence of prostate cancer. The other 75% of prostate cancer tissue biopsies are reported as “negative”.

Though it cost a bit more, Nascent Iodine is more palatable (less caustic) for oral usage and this is what I recommend for children. Lugol’s I reserve for transdermal application. At very high dosages we are talking about treatment costs of approximately 70 dollars a month at maximum doses. Meaning you can do iodine for more than a thousand months before you would spend what you would for having protons warped into your gland. This is the treatment to go for as is sodium bicarbonate, which we will talk about in depth below; we will see in the end which is the best way to go at any price or cost.

A study conducted at University of Illinois has found an interesting
relation between prostate cancer and daily consumption of broccoli and
tomato. Both these vegetables have been known to contain compounds that
can fight cancer. These compounds seem to work better in combination.4

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Selenium also is highly indicated as a more than valuable supplement.   A 1996 study by Dr. Larry Clark of the University of Arizona showed just how effective selenium can be in protecting against cancer. In the study of 1,300 older people, the occurrence of cancer among those who took 200 micrograms of selenium daily for about seven years was reduced by 42 percent compared to those given a placebo. Cancer deaths for those taking the selenium were cut almost in half, according to the study that was published in the Journal of the American Medical Association on December 25, 1996. In addition, the men who had taken selenium had 63 percent fewer prostate cancers, 58 percent fewer colorectal cancers, 46 percent fewer lung cancers and overall 37% fewer cancers. Selenium was found to reduce the risk of lung cancer to a greater degree than stopping smoking.5

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There are now seven population studies in the past six years
 that examined the possible connection between selenium and
prostate cancer. All but one of them has found selenium protective.
                                                                                         Karen Collins, R.D.

Also it makes more than perfect medical sense to increase intensely magnesium cellular (not serum) levels. Why because, “There is reasonable evidence to suggest that calcium may play an important role in the development of prostate cancer,” says Dr. Carmen Rodriguez, senior epidemiologist in the epidemiology and surveillance research department of the American Cancer Society (ACS). Rodriguez says that a 1998 Harvard School of Public Health study of 47,781 men found those consuming between 1,500 and 1,999 mg of calcium per day had about double the risk of being diagnosed with metastatic (cancer that has spread to other parts of the body) prostate cancer as those getting 500 mg per day or less. And those taking in 2,000 mg or more had over four times the risk of developing metastatic prostate cancer as those taking in less than 500 mg. Magnesium chloride or what is known as magnesium oil is the first item of importance on all my protocols. Please see Magnesium for Life site for more information.

Calcium and magnesium are opposites in their effects
on our body structure. As a general rule, the more
 rigid and inflexible our body structure is, the
 less calcium and the more magnesium we need.

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It is no surprise to find another Harvard study in October 2001, which looked at dairy product intake among 20,885 men and found men consuming the most dairy products had about 32% higher risk of developing prostate cancer than those consuming the least High magnesium intake reverses calcification damages and inflammation when used intensely.

High calcium levels interfere with Vitamin D and
subsequently inhibit the vitamin’s cancer protective
 effect unless extra amounts of Vitamin D are supplemented.6

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In this second half of this chapter we are going to focus on two other treatments that come at the exact other end of the spectrum from expensive proton therapy. First is sodium bicarbonate therapy, which is like a kind of natural chemotherapy that can be done easily and safely by anyone for less than five dollars and the other is prostate massage, which can be self administered for free or done by medical doctors. The two together with a full spectrum natural chemo protocol behind them would not only be highly cost effective for individuals and society but by all indications they would be effective and safe to do.

Even if one wants to spend a fortune on more dangerous treatments both sodium bicarbonate and prostate massage should be required adjunct therapies since they can only improve results and reduce and buffer the toxicity and harm of aggressive chemical and radiation treatments. Actually both of these treatments and all the concentrated nutritional medicinals above offer us a nothing to lose and everything to gain treatment for prostate cancer.

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Hormone deprivation therapy causes tumours to shrink;
 however, it’s not a cure. The tumours eventually regrow
 into a stronger form, becoming resistant to treatment.7

With the latest advancements in our understanding of concentrated nutritional medicines we can now confidently present a protocol that makes doing nothing and waiting into an idiot’s option. We really don’t have to wait for innovative, improved and advanced treatment options for they exist already and the medical science is plentiful to backstop the use of the substances presented here.

Sodium Bicarbonate Cancer Treatment

Studies have shown how manipulation of tumour
pH with sodium bicarbonate enhances chemotherapy.8

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Coloured scanning electron micrograph of two prostate cancer cells in the final stage of cell division. Photograph: VVG/Science photo library

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A healthy pancreas secretes sodium bicarbonate to neutralize stomach acid and create an optimal pH environment for pancreatic enzymes. Some of these enzymes circulate in the blood to destroy cancers that occur. Too much iron interferes with the ability of the pancreas to generate sodium bicarbonate and can lead to insulin resistance. Diabetes and cancer are linked because an unhealthy pancreas advances both diseases.

pH of the blood is the most important factor to
determine the state of the microorganisms in the blood.

What is not generally understood is how basic to health pH and bicarbonate levels are and how easily we become acidic, which is an open invitation to have cancer visit ones life. These cancer cells look like yeast and fungi and you know what, many of them are and even mainstream oncology admits quite a bit of that. But whatever our definition and concept of cancer, it does not change the fact that cancer does not like what bicarbonate brings to the body. Most oncologists have no idea about how bicarbonate and CO2 are related and that bicarbonate deficiency leads to CO2 deficiencies in the blood. When our CO2 levels drop so do the levels of O2 and we do see cancer develop under low O2 and high acid conditions.

Our body pH is very important because pH controls the speed of our
 body's biochemical reactions. It does this by controlling the speed of enzyme activity as well as the speed that electricity moves through our body.

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In my book Sodium Bicarbonate, Rich Man’s Poor Man’s Cancer Treatment I write: Most of us are going to be surprised to find out that there is an oncologist in Rome Italy, Dr. Tullio Simoncini, destroying cancer tumours with sodium bicarbonate. Sodium bicarbonate is safe, extremely inexpensive and unstoppably effective when it comes to cancer tissues. It’s an irresistible chemical, cyanide to cancer cells for it hits the cancer cells with a shock wave of alkalinity, which allows much more oxygen into the cancer cells than they can tolerate. Cancer cells cannot survive in the presence of high levels of oxygen. Sodium bicarbonate is, for all intent and purposes, a killer of tumours. At a pH slightly above 7.4 cancer cells become dormant and at pH 8.5 cancer cells will die while healthy cells will live.

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Sodium bicarbonate possesses the property of absorbing heavy
metals, dioxins and furans. Comparison of cancer tissue with
healthy tissue from the same person shows that the cancer tissue
has a much higher concentration of toxic chemicals, pesticides, etc.

This has given rise to a variety of treatments based on increasing the alkalinity of the tissues such as vegetarian diet, the drinking of fresh fruit and vegetable juices, and dietary supplementation with alkaline minerals such as calcium, potassium, magnesium, cesium and rubidium. But nothing can compare to the instant alkalinizing and oxygenating power of sodium bicarbonate for safe and effective treatment of cancer.

Cancer is actually a four-letter word — ACID,
especially lactic acid as a waste product due to the
 low oxygen level and waste products of yeast and fungus.

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There are a multitude of methods to apply sodium bicarbonate and some of the best ways have hardly been tried by anyone. For prostate cancer Dr. Simoncini recommends that, “If there has been no surgical operation, it is possible to attempt firstly to treat the neoplasia through urethral catheters which allow the spreading of the saline solutions inside the prostatic lobes through the ducts. To this it is possible to associate periglandular infiltrations implementable transrectally by utilising very long needles of the type used for amniocentesis.”

In my book, which is the first complete medical review of sodium bicarbonate in existence, I turn my back on Dr. Simoncini’s methods of bicarbonate application but do recognize him as a medical hero and genius. In the book was a testimony from a man whose prostate cancer had spread to his bones and after two weeks of high oral use he tested negative. Dr. Simoncini himself recognizes that for bone cancers his IV treatments are not effective and here we have a prostate patient resolving his bone cancer through oral means, which is safer and certainly hugely less expensive and widely more available.

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Though I believe in Simoncini’s work there are few doctors using his methods because of serious complications that would visit such practitioners by their local medical boards. But no matter, it is good news for humanity to have a universal way to treat cancer, which bicarbonate becomes if used orally and transdermally. Doctors all too often neglect to factor cost as we clearly see in orthodox oncology’s approach to prostate cancer. How can we compare spending $2.61 for a pound of sodium bicarbonate that we can eat and make into a liquid and apply all over our body with spending thousands of dollars for the same thing just so it can be administered through a needle?

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Most practitioners are new to natural transdermal medicine and how its power and safety can be brought to bear on glands like the prostate. Transdermal sodium bicarbonate treatments are even newer than Transdermal Magnesium Therapy, which is the title of my first book in print. Transdermal iodine therapy’s fame though goes all the way back to the American Civil War when iodine was used as a universal medicine.

Prostate cancer demands we systemically take the pH up over eight  and through oral means we can do this and have that pH register in all the tissues of the body.  But we can also put a high concentration of bicarbonate in an enema and combat not only intestinal cancer and strong yeast overgrowth that way but we can have this treatment touch on the tissues intimate to the prostate area. Iodine can also be applied directly to the prostate tissue areas transdermally using a long swab or applying it liberally to genital areas and the perennial area though again oral administration is a must.  Tullio Simoncini uses bicarbonate targeted  more directly to the prostate thru the artery providing its blood supply.

image
A clump of prostate cancer cells. The bluey-green cells are actively growing, whereas
 the pink ones are in the process of dying by programmed cell death (apoptosis)    

 

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Tumors are not distinguishable from the infections that inhabit them. Dr. Marijah McCain identified the primary cause of death in  cancer patients to be not the cancer itself, but fungal overgrowth.

Dr. Simoncini says, “At the moment, against fungi there is no useful remedy other than, in my opinion, sodium bicarbonate.” Bicarbonate is a chemo agent and in fact is used in oncology with its horrid list of chemo agents but it is used to buffer the effects of the dangerous chemo chemicals. Traditional chemo is just much too dangerous to do without sodium bicarbonate meaning the side effects would escalate beyond acceptable limits if not used. In fact, so dangerous and toxic are most chemo chemicals that many people would die on the spot without softening the blow with bicarbonate.

We do not have to fear bicarbonate intake. And in fact, people who live in areas of the world with high amounts of bicarbonate in their drinking waters have a striking decreased mortality rate and a decreased prevalence of disease. Sodium bicarbonate, though often used as a medicine, is unlike pharmaceutical compounds. It is a natural non-toxic substance that does not require clinical trials for an assessment of toxicity. Spring waters contain bicarbonate ions which are coupled mainly with sodium, potassium, calcium or magnesium ions. A deficiency of bicarbonate ions in the body contributes to a range of diseases and medical conditions.

The Prostrate and Sex

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When it comes to men, numerous researchers have shown that a high ejaculation frequency and sexual activity are linked to a lower risk of prostate cancer later in life. An epidemiological study of 30,000 men showed that men who ejaculated 13 to 20 times monthly presented a 14% lower risk of prostate cancer than men who ejaculated on average, between 4 and 7 times monthly during most of their adult life. Those ejaculating over 21 times a month presented a 33% decreased risk of developing prostate cancer than those on the baseline.

Orgasm acts as a powerful pain-relief agent, and studies
 suggest it bolsters immune functioning. The typical orgasm
 will boost the body’s T3 and T4 lymphocyte cells—the
cells that fight off foreign invaders—by up to 20 percent.

Michael Leitzman, a cancer researcher at the National Cancer Institute in Bethesda, Maryland and author of the above mentioned study, explains that there has been a suggested link with greater sexual activity and increased incidents of prostate cancer in previous scientific data because of the link with the male hormone testosterone and its effect on promoting cancer cell growth. But he says this theory has its shortcomings because testosterone levels alone do not predict prostate cancer risk and they do not appear to correlate with sexual desire as much as previously thought. Instead, researchers say ejaculation may protect the prostate through a variety of biological mechanisms that merit further research, such as:

•Flushing out cancer-causing substances. Frequent ejaculation may help flush out retained chemical carcinogens in the prostate glands.

• Reducing tension. The release of psychological tension that accompanies ejaculation may lower nervous activity associated with stress and slow the growth of potentially cancerous cells in the prostate.

• Promoting rapid turnover of fluids. Frequent ejaculation may help prevent the development of mini-crystals that can block ducts within the prostate gland, reducing cancer risk.

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Prostate Massage

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image

When men get older an enlarged prostate is a common problem. Fat and proteins can accumulate and enlarge the prostate gland to a degree where pain happens and urinating becomes a problem. A prostate massage is a good way to drain the prostate. Even if you do not have any problems with your prostate yet, it is recommended that you do a massage once a month to prevent problems. If you already have problems a daily massage may be needed to reduce pain and swelling but of course you should be taking medicinals like magnesium chloride. which will reduce the inflammation and clear out excess calcium from the area; iodine to deal with any infection and sodium bicarbonate which will flood the area with O2 and alkalinity. Although thought in terms of pleasure, prostate milking, another word or level of prostate massage, is performed for medical reasons.

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Inserted Note: (not in original): prostate massage can be accomplished as described here, generally a "manual massage" but there are numerous "devices" that allow this to be done with more privacy and probably more effectiveness.

Here is an enlarged image of the manual method, showing the area inside the body where the massage takes place.

 

Massage of The Prostate -- Cancer Treatment

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One source of the "device" that can be used is here:

The majority of men have not even heard of prostate stimulation or have any concept of what it is. However, for those who have and had the pleasure to experience prostate stimulation, you are not likely to forget it!

More and more men are looking to learn about and experience prostate stimulation for two main reasons. For most men, the most important reason is for pleasure beneifts. Men who experience a prostate orgasm from male prostate stimulation say it is much stronger and lasts much longer than a typical male orgasm.

As well, men ejaculate substantially more fluid from prostate stimulation. This is part of the reason why prostate stimulation can be great for prostate health is the release of large amounts of prostate fluid. This can help relieve painful prostate problems made worse by a build up of extra prostatic fluid.

You can stimulate your prostate by several ways. You can use the manual method that involves using your finger, or purchase a prostate massager. Both ways can be effective but you need to know the proper techniques for male prostate stimulation to be easy,safe and effective.

Prostate massage is the most common way to stimulate the prostate. A prostate stimulation video can be helpful in learning the proper ways to perform a prostate massage. (SOURCE)

Here is another source:

 

prostate massage animation

 

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The source with this image also has this text:

Prostate massage has long been used as a means of maintaining prostate health and to promote increased sexual health. In the Orient, prostate massage has been included in traditional medicine for centuries. In recent years, many medical articles have been published which advocate prostatic massage as a treatment for chronic prostatitis, infertility, and benign prostate hypertrophy (BPH).

Historically, prostate massage has been used for centuries as a part of Oriental & Ayurvedic holistic health practice. Prostate massage is once again becoming more widely recommended as researchers discover that prostate massage complements and increases the effectiveness of antibiotics, antimicrobials or herbal remedies by facilitating circulation to the prostate gland. In addition, many find that prostate massage itself is successful where other remedies have failed. (source)

 

Electric Muscle Stimulator Of ProstageAnother source of useful data is here:

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  • Significance

  • The male G-spot, once located and properly stimulated, provides men with an orgasm more powerful than they have experienced with regular intercourse. Prostate milking enables the male to experience multiple orgasms, orgasms that are longer in duration and the ability to ejaculate without being sexually aroused beforehand. It has been claimed that the power of the orgasm can be increased by as much as 400 percent and that the duration of the orgasm can last up to 5 minutes.

    Function

  • The male G-spot can be used to heighten sexual intercourse or as a form of masturbation. The male G-spot is actually a man's prostate, the gland responsible for producing semen. It is located below the bladder and in front of the rectum; it is a bump about the size of a chestnut. It is also referred to as "the feel good gland" because once stimulated, it provides what is known as a full body orgasm.

    Identification

  • To locate the male G-spot, it is best to be lying down with your feet up and legs spread. If you are attempting to locate it yourself, it may be helpful to place something under your bottom, making it easier to reach the perineum. If it is your first time attempting this, go slow and use lubrication. Be sure that the sphincter (the muscle controlling the release of feces), is relaxed. Gently insert your finger into your anus and probe slowly. You will know you've reached the prostate gland when you come across the chestnut-size bump that is roughly 2 inches inward.

    Considerations

  • Before you or your mate begin prostate milking, it is best to get as relaxed as possible. Sometimes taking a hot shower beforehand will help with this. Using a finger is the best way to locate and provide stimulation to the G-spot if you are a novice, but there are sexual devices that can enhance your experience as well. There are also different techniques that can be used. Having your mate perform oral sex while stimulating your G-spot is one option.

    Misconceptions

  • There has been so much speculation about it being strange and perverse for men to locate their own G-spot that many men have not talked about or attempted it. The fact of the matter is that prostate milking is as normal as regular intercourse, it is not perverse, is not only for gay men, and it does not make one strange for enjoying the pleasure associated with it. It is a very powerful sexual gland that can lead to intense orgasms, and it is perfectly normal to experiment with it.

    Warning

  • There are some risks associated with prostate milking if it is not performed correctly. Applying too much pressure on the prostate gland could lead to serious health conditions such as Fournier's gangrene, hemorrhoidal problems, blood poisoning and transferring prostate cancer to various parts of the body. The amount of recommended pressure on the G-spot is comparable to the amount of pressure you would use to rub your eyes with. (source)
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“Part of the role of the prostate gland is to produce a clear fluid which makes up about thirty percent of male seminal fluid and, in cases of chronic prostatitis or benign prostatic hyperplasia, prostate milking can be used to reduce pressure in the prostate gland by removing excess fluid. Although it is possible to perform prostate milking externally by stimulating the prostate through the perineum this method is not always successful and it is more usual for prostate milking to be performed internally using a finger, prostate massager or a medical massager,” writes Donald Saunders, who gives clear instructions for how to do it oneself.9 (See reference for complete instructions.)

image

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Doing prostate massages on oneself or having it done as a medical procedure or perhaps by a colonic specialist is not a joke. Prostate massage is part of the digital rectal examination (DRE) routinely given to men by urologists in order to look for nodules of prostate cancer and to obtain expressed prostatic secretions (EPS) for examination under microscope. Many instruct men to do this in order to keep the prostrate healthy. The massage does not only increase your health but can also improve your sex life and this is very important to men and their emotional health.

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During that initial visit, Dr. Zeitlin had to massage my gland twice to get the fluid out, and I think this accelerated my improvement. I felt much improved (say, 60% better) one week after the massage. I went back for a second massage one week later. It was painful, but he did drain more fluid...and today, one week later, I feel about 85% improved. After four months of agony, this is nothing short of miraculous to me. My bladder symptoms are all but gone. My perineal pain is all but gone.10

If you have an enlarged prostate then a prostate massage can clearly help. Massaging the prostate gland brings fresh blood and oxygen to the normally congested and suffocating prostate gland. Viruses, bacteria and fungus are just waiting for the right conditions in which to begin rapid multiplication. Rot is an underlying biological mechanism and infection is a natural process of biological decay, which congestion and blood stagnation encourages.

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Fresh healthy blood is healing to tissues and milking the prostate gland also all keeps all the sexual fluids (semen) fresh, clean, and moving out of the body. When fluids stagnate or blood and oxygen flows diminish disease thrives. In cases of chronic prostatitis (an inflammation of the prostate gland) or an enlarged prostate (benign prostatic hyperplasia, or BPH) prostate milking can be helpful in reducing pressure in the prostate gland by removing excess fluid.

The prostate gland in many men suffers from blood congestion and stagnation when they are underactive sexually. When semen stagnates, it starts to decompose and becomes a breeding ground for bacteria and virus. The prostate needs a plentiful supply of fresh blood to nourish it with food and oxygen. And equally important, the prostate needs plenty of blood flow and regular semen release to keep clean, healthy and pain free. A man's prostate gland needs to be stimulated to discharge its load. If this is not done often enough, there would be a build-up of fluid secretions and this gland or sac that holds the fluid will be inflamed and infected. This stagnation of seminal fluid is one of the many causes of prostate cancer.

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One should do a massage at least once a month for about 10 to 20 minutes if one is concerned about the health of their prostate. It certainly would be a good thing for doctors to recommend to their male patients. There are things called prostate massagers, which you place on a chair, sit on it and use your own body weight to perform the massage and others that you simply insert.

One-third of the men with initial prostate cancer tissue
 biopsies that are reported as “negative” for prostate cancer
 actually do have prostate cancer that was missed by the biopsy.

If you are suffering from as yet undiagnosed prostate cancer then cancerous cells could be broken up and distributed not only spreading cancer within the prostate gland but also causing it to metastasize and thus spread to other areas of the body. If one is diagnosed the prostate massage becomes an important part of ones treatment but it is essential to target the cancer with bicarbonate, iodine, magnesium chloride and selenium before one starts on ones massage routine. The idea is to completely change the condition not only inside and around the prostate gland but systemically as well so further cancer growth is not encouraged or allowed.

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Emotional Profiles are Important

Some researchers have found that the average victim of breast or prostate cancer was unable to express such basic drives as anger, aggressiveness, or sexual impulses, suffered from an inner turmoil "covered over by a façade of pleasantness." In Psychosomatic Medicine, California's Dr. Eugene M. Blumberg and his colleagues report on patients with a wide variety of cancers: "We were impressed by the polite, apologetic, almost painful acquiescence of the patients with rapidly progressing disease, as contrasted with the more expressive and sometimes bizarre personalities of those who responded brilliantly to therapy with long remissions and long survival."

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Cancer is a message to us – it’s a loud scream from our
 bodies.  It is communicating to us that something is not quite
 right within us emotionally, physically, mentally and even spiritually.

Dr. Bernie Siegel said, “I have collected 57 extremely well documented so-called cancer miracles. A cancer miracle is when a person didn't die when they absolutely, positively were supposed to. At a certain particular moment in time they decided that the anger and the depression were probably not the best way to go, since they had such a little bit of time left, and so they went from that to being loving, caring, no longer angry, no longer depressed, and able to talk to the people they loved. These 57 people had the same pattern. They gave up, totally, their anger, and they gave up, totally, their depression, by specifically a decision to do so. And at that point the tumors started to shrink.”

Conclusions

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One in three breast cancer patients today may be treated unnecessarily and thus incorrectly according to a 2009 study.11 We can infer, without such a study for prostate patients, that the story would be uniformly the same for them. Cancer sufferers en mass are being forced to pay with their lives for the incredible arrogance of oncologists and medical officials who refuse to open their eyes to see the medically sound solutions that are already out there. Why should our loved ones suffer for their ignorance?

There are many ways to treat cancer and new ideas are constantly being presented and then ignored. A study published in the European medical journal Anticancer Research demonstrates a substance used as a cough suppressant for over fifty years may be useful in treating advanced prostate cancer. Researchers from the Prostate Cancer Research and Educational Foundation, the MedInsight Research Institute, and the University of California in San Diego found that noscapine, a non-addictive derivative of opium, reduced tumor growth in mice by 60%. What's more, it halted the spread of tumors by 65% and caused no harmful side effects. Medical marijuana, especially when taken in the form of oil, is also known to arrest cancer while it simultaneous deals with the mental emotional makeup of the cancer sufferer as it reduces pain and emotional upset.

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Part of any successful cancer treatment includes
chelation and detoxification of heavy metals and a host of
 toxic chemicals, which are all invading our bodies’ everyday.

Spices add flavor to food but also may have cancer-fighting properties. India has one of the lowest cancer rates in the world, and the people there typically eat a diet containing a wide variety of spices. There is some limited evidence that capsaicin, the component of chile peppers that makes them hot, has some anti-cancerous properties. Both curry and cumin contain turmeric, which has been found to have anti-carcinogenic properties in cell cultures.12 In studies involving mice, curcumin has demonstrated anti-carcinogenic activity in a variety of cancers.13 A compound in aged garlic significantly inhibited the growth of human prostate cancer cells in vitro.14 There is so much we can do for ourselves but there the medical system insists that we either do nothing or surrender to the scalpel or dangerous radiation machines.

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One should seriously consider changing one’s diet and pay close attention to the quality of ones water and how much water one drinks. Using super foods like spirulina or wheat grass juice are wonderful therapies as are colonics or natural enemas, getting lots of body work and even acupuncture has clearly demonstrated its usefulness for prostate patients. Literally there is no end to the things one can do to help oneself including taking hot therapeutic baths loaded with magnesium, bicarbonate and even sodium thiosulfate.

It is shocking how many people die from cancer even after governments have thrown the kitchen sink at it. After hundreds of billions spent on research people are still dropping dead at close to the same rates as years past but no one thinks that the medical establishment is at fault. It literally cost me nothing to put this information and essay together yet medical officials and organizations don’t want the public to have easy access to these kinds of treatments.

Sodium bicarbonate is a nothing-to-lose-
everything-to-gain-cancer-treatment.

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Every man should have all this information in his hands and every woman who has a man she loves should have it as well. But the vast majority will not receive it because the channels of mass communication are blocked and controlled by the elite who really do mean us harm. They want to hurt us and our loved ones but they will never admit that. They enjoy having us in their hands because they profit from it. The profit motive does not belong in the field of medicine and certainly not in oncology were it’s a matter of life and a promised miserable death. Capitalism certainly has shown its ugliest face in the vast field of medicine, which sucks up a huge percentage of GNP, and even so does a miserable job.

With the guidance of an enlightened healthcare practitioner
or doctor, and with the right protocol and multidimensional
 approach there is really no reason why a man has to die of
prostate cancer or subject himself to harmful radiation or
surgery. The same goes for woman and their breast cancers.

 

Mark Sircus Ac., OMD
Director International Medical Veritas Association

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_________________________________________________________

3 through the years, Stamey has come to believe that the PSA test is actually not a useful predictor of the amount or severity of prostate cancer. He said elevated levels of that protein, prostate specific antigen, a protein normally produced by the prostate gland. actually reflect a condition called benign prostatic hyperplasia, a harmless increase in prostate size.

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4 Dr. Q.Y. Lu and colleagues from the University of California at Los Angeles found that, "These avocados were found to contain the highest content of lutein among commonly eaten fruits as well as measurable amounts of related carotenoids (zeaxanthin, alpha-carotene, and beta-carotene). Lutein accounted for 70% of the measured carotenoids, and the avocado also contained significant quantities of vitamin E. An acetone extract of avocado containing these carotenoids and tocopherols was shown to inhibit the growth of both androgen-dependent (LNCaP) and androgen-independent (PC-3) prostate cancer cell lines in vitro. Incubation of PC-3 cells with the avocado extract led to G2/M cell cycle arrest accompanied by an increase in p27 protein expression."

5 Clark LC. The epidemiology of selenium and cancer. Fed Proc 1985; 44:2584-2590.

6 Accu-Cell Nutrition; Calcium and Magnesium www.acu-cell.com/acn.html

8 Enhancement of chemotherapy by manipulation of tumour pH. Raghunand N, He X, van Sluis R, Mahoney B, Baggett B, Taylor CW, Paine-Murrieta G, Roe D, Bhujwalla ZM, Gillies RJ. Arizona Cancer Center.

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It is very important to milk the prostate gland from the top to the bottom, squeezing it gently all the way down. Never use undue force and always perform prostate milking as gently as possible and with just sufficient force to stimulate the prostate gland. If you think in terms of the force used when gently massaging a tired eyeball this is about the right pressure.

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There are several potentially serious consequences to over-vigorous milking: If you are suffering from prostatic calculi (small stones within the prostate gland) these can act rather like scouring grit and tear the delicate membranes of the gland. The rectal lining in the area of the prostate gland is very thin and can easily be perforated.

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The best instrument for milking the prostate gland is an Aneros prostate massage device. It is designed to give a perfect prostate massage and prostate milking. The difference when milking the prostate gland (rather than massaging the prostate) is that you will push the Aneros all the way in, apply pressure to your prostate, and then manually run the Aneros down over the full length of the gland.

During a prostate massage, you simply squeeze the Aneros with your anal contractions. If you do the massage by hand, simple use your fingers (your middle finger). However, your fingers (middle finger) may be too short to reach the prostate gland, so try it out and use the massager otherwise. Because of the angle it may not be so easy. Risk is low that you hurt yourself. Try to find the middle of your prostate and start the massage. You can find a ridge or indentation there. You can massage the prostate until fluid leaks out. This is also called milking the prostate. If possible urinate after the drainage to wash it away. Usually you can feel the fluid move during the massage. This is a sign that you are doing it right. Your prostate can be swollen quite a lot so finding it should be easy. Slow continues pressure is the best. If you really have a very swollen prostate with a lot of pain then you could do a massage and drainage daily.

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ezinearticles.com/?The-Ins-And-Outs-Of-Prostate-Milking-Or-Prostate-Massage&id=640873

1. Before attempting prostate milking pay a visit to the bathroom to ensure that both your bladder and bowel are emptied.
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2. Ensure that your fingernails are trimmed short and that your hands and the area around your anus are washed thoroughly.
3. Put a sterile latex glove onto the hand which you wish to use to massage the prostate gland and apply some water-based lubricant to your gloved fingers.
4. Adopt a comfortable position. The position which you adopt is not important as long as it is comfortable and allows you to gain easy access to the prostate gland with your gloved hand. Most people find that lying on their back or side is most comfortable.
5. Gently insert your finger (or fingers) into your anus and move it slowly forward along the wall of the rectum, as if you are heading for your belly button, until you feel the prostate gland. The prostate gland will feel like part of a small ball and is normally about the size of a walnut.

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6. Having located the prostate gland, massage it gently along both sides but do not massage the central (top) area which contains several sensitive nerves.
7. After a few minutes of gentle milking the gland will be sufficiently stimulated to contract causing it to release its fluid. At this point you might experience a degree of sexual pleasure and, in some but not all cases, may also experience orgasm.
Prostate milking should not be performed if you are suffering from an acute case of prostatitis and should never be performed vigorously.

10 www.prostatitis.org/ProstateMassageBiopsy.html

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11 Karsten Jorgensen and Peter Gotzsche of the Nordic Cochrane Centre in Copenhagen analyzed breast cancer trends at least seven years before and after government-run screening programs for breast cancer started in parts of Australia, Britain, Canada, Norway and Sweden. The research was published in July of 2009 in the BMJ, formerly known as the British Medical Journal.

12 Rao CV, et al. Chemoprevention of colon carcinogenesis by dietary curcumin, a naturally occurring plant phenolic compound. Cancer Res 1995; 55: 259-66.

13 Huang MT, Newmark HL, Frenkel K. Inhibitory effects of curcumin on tumorigenesis
in mice. J Cell Biochem Suppl 1997; 27: 26-34.

14 Raloff J et al. Radical prostates. Science News 1997 151: 126-27.

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Legal Notice: The Author specifically invokes the First Amendment rights of freedom of speech and of the press without prejudice. The information written is published for informational purposes only under the rights guaranteed by the First Amendment of the Constitution for the United States of America, and should not in any way be used as a substitute for the advice of a physician or other licensed health care practitioner. The statements contained herein have not been evaluated by the FDA. The products discussed herein are not intended to diagnose, cure, prevent or treat any disease. Images, text and logic are copyright protected. ALL rights are explicitly reserved without prejudice, and no part of this website may be reproduced

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3.4

My About-Face on the PSA Test Why every man should have this prostate test done today!

Karl Note: This small part of this article? I found, but could not download the remainder -- this is left here incomplete.

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Source

This report may come as a real shock to you. I’m officially doing an about face on the PSA test.


For years, I’ve told you that I don’t believe in the usefulness of the PSA test. And that I had never gotten one myself — until now.

That’s all changed.

And you need to know why.

I’ve recently discovered that the PSA test could save your life. But not in the way you may think.

In 2004, American Cancer Society statistics show that 32,000 men died from prostate cancer in the U.S. Doctors diagnosed over 232,000 new cases in the same year. In fact, prostate cancer is the most common malignancy to affect men. It’s the second leading cause of cancer death in men after lung cancer. And the incidence is escalating

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3.5

FAKE Source of Data About Prostate Cancer

 

Source

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Karl Note: The reason I label this data as "fake" is that I discovered an amazing thing about the reduction in value of the Google Search Service, and wrote about that HERE. Nontheless, I've included this "fake information" here since that may be all that can be found -- no longer can you expect to find any "personal opinion" with a name attached to that opinion. Click on the "source" link above to explore just how deceptive this web site, and therefore, the data from it are.

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If prostate cancer is caught before reaching the end stage, then it is often treated very successfully. Treatment has been getting higher and higher success rates within the last twenty years, although it is still not known what causes the cancer and how to prevent it.

However, if the cancer spreads from the prostate gland to the bone then it becomes extremely difficult and often impossible to cure. In this situation treatments are aimed at prolonging life and relieving symptoms rather than curing.

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When a cancer reaches its end stage the patient may start to show signs such as weight loss, tiredness and pains in different places. In the case of prostate cancer, this is especially true in the lower back and hips.

Prostate cancer is the second most likely cause of death to a man in cancer related deaths. If left untreated and provided the man does not die of other reasons, it will cause death. As it is a slow developing cancer, in many cases the man may die of other causes before being killed by the cancer. This is especially true as prostate cancer is much more likely to occur amongst older men, and can take 15 years or more to full develop.

If the cancer has reached an un-curable stage, then treatments can be effective at reducing pain and prolonging life, although as has been said once the cancer spreads to the bone it is usually untreatable.


 

Karl Note: This below is the type of "theety-weety" pablum that you can find with most web search results -- JUNK. If you find something different, it will ususally be selling some snake oil. Web sites that offere apparently valuable information often won't let you see it without providing at least your eMail address and most often your complete name and address -- before you get the goody. Beware such places, they sell your name to hundreds so you can expect to get lots of spam junk.

All content at ProstateCancerFAQ.org is for informational purposes only. We do not give medical advice, nor do we provide medical or diagnostic services. We strongly emphasize that the content provided on this website, by the admin, or any of its authors, is not to be substituted for professional medical advice, diagnosis or treatment. Always consult with your doctor or other qualified healthcare provider. Never disregard professional medical advice or delay in seeking medical treatment because of something you have read, seen or heard on ProstateCancerFAQ.org The site is provided to you on an "as is, with all faults" basis. 

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3.6

Suggestion From Karl's Close Friend Dr. MSR Ayyangar, Mumbai, India

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Karl Note: Dr. MSR Ayyangar is an Ayurvedic Physician, a Doctor of Homeopathy in regular practice in Mumbai, India, knows Karl Loren and his family personally from visits to the USA, staying at the residence of Karl in 2008 and earlier. Dr. Ayyangar is a man of great credentials, worldwide, including the following he sent along with his suggested protocol:

Dr. Ayyangar: I just returned from a lecture tour (15th to 20th) of South India having delivered lectures on "Green Chemistry" sponsored by different departments of Government of India connected with environment - and - spiritual philosophies in Management in Business schools. The organizers insisted on my being the "Chief Guest" during the seminar ... though I insisted that I have no knowledge on this field of chemistry. But in the final reckoning ... only I was quoted by all the News Papers with my Photograph being prominent & TV Channels extensively showing their interviews with me.

I am suddenly named by news papers as ... "Haritha Rasayana Saasthra Nipunudu" meaning "Great expert on Green Chemistry" in Telugu language.

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Selenium (Selenomethionine) + Pycnogenol .... is a very good choice for you. Normally Prostate Cancer is benign, self limiting and does not quickly tend to become malignant or spread and become metastatic. There are now laparoscopic methods available to remove Prostate Gland with minimal collateral trauma to the surrounding tissue.

For alkaline water, simple addition of "pure" Carbonate of Potassium or Calcium in your drinking water is good enough as they automatically form Hydroxides. Buy a simple dip pH meter (like Thermometer) to help you keep and maintain the water you drink at pH 8.00.

Keep me regularly posted on the developments.

Kindly,
Dr. Ayyangar.

Click Here for Photo Slide Show of Dr. Ayyangar and his wife, visiting with Karl Loren and his family, including Mr. Clifford Woods.

 

3.8

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Source

Scientific evidence shows vitamin D may go beyond its traditionally known role in maintaining bone integrity, according to new research presented at the Institute of Food Technologists Annual Meeting and Food Expo® earlier this month. It may play a role in preventing autoimmune dis-eases or over-acid tissue conditions such as multiple sclerosis and rheumatoid arthritis, some types of cancerous conditions such as breast, ovarian, colorectal and prostate.

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Advancing technologies to add vitamin D to natural foods create offerings that provide excellent sources of both vitamin D and calcium which can help consumers achieve dietary adequacy of these largely under-consumed nutrients.

Recent headlines tout vitamin D as the new wonder supplement, with claims ranging from its ability to reduce cancer risk to its link to cognitive function in older men. While studies show connections exist, experts debate the amount of vitamin D necessary for optimal health, however.

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"Low vitamin D status is linked to a number of different conditions," said James C. Fleet, Ph.D. professor in the department of foods and nutrition at Purdue University. "These include certain cancers, muscle weakness and types I and II diabetes--possibly even schizophrenia and multiple sclerosis."

Muscle weakness in cases of low levels of vitamin D may be explained by muscle's low levels of vitamin D receptors. "Studies with mice show that without vitamin D receptors, cells can't absorb the vitamin," said Dr. Fleet. "Research also shows a correlation between high vitamin D status and improved lower body muscle function in men and women over 60 years old."

Studies also show a decrease in colon cancer with an increase in vitamin D status, and it seems protective against other acidic cancerous risks as well. "One theory is that vitamin D may indirectly inhibit pro-cancer pathways," said Fleet. "The question is finding the protective level, which remains under some debate."

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Although it remains controversial, 30 nanograms/milliliter (ng/mL) of vitamin D is associated with fewer fractures and falls, according to Karen Hansen, assistant professor of medicine within the rheumatology section at the University of Wisconsin. "Vitamin D deficiency causes osteoporosis by triggering decreased calcium absorption, secondary hyperparathyroidism, increased bone resorption and decreased bone mineral density." Study variables and inconsistencies make further studies necessary. Currently, 700 to 800 International Units (IU) of vitamin D a day seems most effective.

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According to Dr. Robert O. Young, Director of Research at the pH Miracle Living center, "recommendations for an "adequate intake" of vitamin D should be at 50,000 IU's for maintanance and 100,000 IU's in any acute or chronic condition, including diabetes, MS, heart dis-ease and cancerous conditions."

 

3.81

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Vitamin D Helps To Prevent Cancerous Breasts and Tumor Formation

By Dr. Young

Source: Private eMail to Karl

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A connection between vitamin D level and the risk
of developing cancerous breasts has been implicated
for a long time, but its clinical relevance had not
yet been proven. Sascha Abbas and colleagues from
the working group headed by Dr. Jenny Chang-Claude
at the German Cancer Research Center (Deutsches
Krebsforschungszentrum, DKFZ), collaborating
with researchers of the University Hospitals
in Hamburg-Eppendorf, have now obtained clear
results:

While previous studies had concentrated chiefly
on nutritional vitamin D, the researchers have
now investigated the complete vitamin D status.
To this end, they studied 25-hydroxyvitamin D
(25(OH)D) as a marker for both endogenous
vitamin D and vitamin D from food intake.

The result of the study involving 1,394 cancerous
breast patients and an equal number of healthy
women after menopause was surprisingly clear:

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Women with a very low blood level of 25(OH)D have
a considerably increased risk for cancerous breasts.
The effect was found to be strongest in women who
were not taking acidic cancerous causing hormones
for relief of menopausal symptoms. However, the
authors note that, in this retrospective study,
diagnosis-related factors such as chemotherapy or
lack of sunlight after prolonged hospital stays
might have contributed to low vitamin levels of
breast cancer patients.

In addition, the investigators focused on the
vitamin D receptor. The gene of this receptor is
found in several variants known as polymorphisms.
The research team of the DKFZ and Eppendorf
Hospitals investigated the effect of four of
these polymorphisms on the risk of developing
cancerous breasts. They found out that carriers
of the Taql polymorphism have a slightly increased
risk of cancerous acidic tumors that carry receptors
for the female acidic sex hormone estrogen on their
surface. No effects on the overall breast cancer
risk were found. A possible explanation offered
by the authors is that vitamin D can exert its
cancerous-preventing effect by counteracting the
growth-promoting effect of the acidic estrogens.

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Besides its cancerous-preventing influence with
effects on cell growth, cell differentiation and
programmed cell death (apoptosis), vitamin D
regulates, above all, the calcium metabolism in
our body. Foods that are particularly rich in
vitamin D include cod liver oil, green fruits
and veggies. However, the largest portion of
vitamin D is produced by our own body with the
aid of sunlight.

According to Dr. Robert O. Young, Director of Research at the pH Miracle Living center, "recommendations for an "adequate intake" of vitamin D should be at 50,000 IU's for maintenance and 100,000 IU's in any acute or chronic condition, including diabetes, MS, heart dis-ease and cancerous conditions."

3.9

 

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Source

ABNORMAL PSA LEVEL/GLEASON GRADE: What is an abnormal PSA level and what are grade levels for prostate cancer?

Answer: Some doctors would say the PSA level is normal if it's below 4 ng/ml and above normal if it's above 4 ng/ml. I believe that the cutoff of 4 is too high and we have used 2.5 as our cut off in our PSA screening study since 1995. We have proven that if the PSA is between 2.5 and 4, there is a 22 percent chance that the man will have prostate cancer. We routinely recommend a biopsy if the PSA is above 2.5 and if the free PSA test confirms the advisability of performing a biopsy. Even men with PSA levels lower than 2.5 might have prostate cancer. In our studies, the median PSA level in men without known prostate cancer was less than 1 in men in their 40s and 50s and less than 1.5 in men over the age of 60. It the PSA level is higher than the median for the age group, the risk of prostate cancer is higher. So, if the PSA level is above the median and especially if it is rising, a biopsy should be considered.

Prostate cancers when looked at under the microscope can look like almost normal prostate tissue or they can look very wild and disorganized. They are graded on a scale called the Gleason grade of between 2 and 10 where 2 is the best, i.e., a low grade, slow growing prostate cancer, and a 10 would be the worst, i.e., a rapidly progressing, very aggressive prostate cancer. It turns out that grade level statistics for prostate cancer fall into a bell shaped curve. Only about 10 percent of tumors are grade 2, 3 and 4 and only about 10 percent of tumors are 8, 9 and 10 with the vast majority being Gleason grades 5, 6 and 7. Gleason grades 8-10 are considered highly aggressive, Gleason 7 is considered moderately highly aggressive (4+3 is considered to be more aggressive than 3+4), Gleason 3+3 is considered mildly aggressive, and Gleason 2-4 is considered so non-aggressive that immediate treatment might not be needed in men over the age of 70.

VIAGRA AND PSA RESULTS:

Q: Does taking Viagra the night before a PSA test affect the results? A week before?
Answer: It can if it results in sexual intercourse with ejaculation. Ejaculation elevates the PSA level for 24 to 48 hours.

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STRESS AND PSA: Is there a known relation between personal stress and PSA results?
A: Not directly. Personal stress can cause sexual dysfunction or lower the body’s resistance to infection. That lowering might lead to prostatitis, and prostatitis can raise the PSA level temporarily.

EFFECT OF SEXUAL ACTIVITY ON PSA MEASUREMENT: Can frequent sex with a penile implant make a PSA level rise?
Answer: Sexual activity can cause a transient rise in the PSA level. This is usually a minimal rise and does not last for more than a 6 to 24 hours. Sex with or without a penile implant does not make a difference. It is ejaculation that causes the PSA to rise. It is ideal to avoid sex for 24 hours before PSA testing.

VARIATION OR ERROR IN PSA TEST: What is the error associated with the PSA exam? What sort of fluctuation in the PSA level would you expect if you ran a PSA test three different times on the same sample of blood?
Answer: If you ran the test on the same sample three times, the error should be no more that 3% or so. If you drew a blood sample on three successive days the variation may be as great as 10-15%.

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HIGH PSA AND BIOPSIES DO NOT SHOW CANCER: My father, aged 54 years, has a PSA of 20. When he first had the test done at age 50,it was 17 and his doctor was reasonably very concerned. Since then, he has gone for a biopsy twice, and has had a total of 12 biopsies taken. All biopsies have come back negative for cancer. The doctors tell him his prostate is only slightly enlarged, and they cannot feel any tumors. He also says that they have found numerous "calcium crystals". Where he should be going from here? My dad really doesn't want to keep going for biopsies because they are very uncomfortable for him. Do you think annual biopsies are reasonable, or is there another test that may detect something the biopsy cannot?

Answer:Our studies show that prostatic biopsies can easily miss prostate cancers. In our recent analysis of more than 2500 men who underwent one or more prostate biopsies, of those who had cancer detected, only 77% had the cancer discovered on the first biopsy. Of the rest, 91% were discovered on the first or second biopsy, 97% on the first three biopsies, and 99% on the first 4 biopsies. Some men required 6 biopsy sessions to detect the cancer. So, with each biopsy session there is increased confidence that the high PSA might not be due to cancer. However, there is a current trend among urologists to obtain more biopsy cores during each biopsy session and to perform the biopsies under local or general anesthesia so that more biopsy samples can be obtained without undue discomfort. It is also important to ensure that the biopsies are directed to the zones of the prostate where most of the cancers are found. In some men the cancer may be located in the central region of the prostate gland where biopsies are not usually directed. Sometimes these cancers can be best detected on transurethral recection biopsies, obtained under anesthesia through a scope that is passed into the central part of the prostate gland. These biopsies are sometimes called “saturation biopsies.” Some men with high PSA values do not have prostate cancer. Other options are to try a long course of antibiotics such as Cipro 500 mg twice a day to see if it brings the PSA down. Other criteria to consider is the PSA density (PSA divided by prostate volume). If it is higher than 0.10, it is worrisome for prostate cancer. Also, measuring the percentage of free PSA (free PSA/total PSA x 100). If it is lower than 25%, it is of concern - and the lower, the more concerning. Certainly, annual biopsies are not unreasonable, especially if the PSA or other parameters continue to suggest a higher risk for prostate cancer.

RISING PSA: My PSA has is up to 6.9 from 1.2. I have known men with PSA of greater than 10. What treatment will my doctor recommend?

Answer:The PSA increase may be due to inflammation in the prostate. So, the first step is to take a 10 to 14 day course of antibiotics (such as Cipro 500 mg twice a day). Of course, if the PSA does not come back down, a biopsy of the prostate should be considered.

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LOW PERCENTAGE OF FREE PSA: I am an active 59 year- old man with bladder cancer (diagnosed almost 3 years ago; stage 1, grade 3-4) which was surgically removed. I received BCG treatments for 18 months and have been watched and examined through cystoscopes, urine tests and blood tests. My PSA tests go between 4.0 and 4.5 and my free PSA tests had been a 6 and now is a 3. I have undergone 2 prostate biopsies with 10 samples taken each time. Cancer has not been found. My question is what could make my percentage of free PSA so low? My doctor has stated that my prostate is large. Are there any suggestions or do we just keep checking with biopsies?

Answer: When the total PSA is between 4 and 10 and the percentage of free PSA is less than 10, there is about a 58% chance that biopsies will show cancer. This means that there is a 42% chance that the biopsies will not show cancer. I would advise that you monitor the total PSA level and the free PSA level, and if the total PSA level rises, consider further biopsies. It is possible that with a large prostate gland, there could be areas of cancer that were missed by the first two sets of biopsies. If you want to be as pro-active as possible, you might want to consider repeating the biopsies again in one year. It is well established that BCG therapy for bladder cancer can induce chronic inflammation in the prostate gland that can result in a long-term elevation of the PSA level.

LOW FREE PSA PERCENTAGE: Besides cancer what else can cause a very low PSA free number?

Answer:There is still much to be learned about free PSA. We now know that there are several forms of it. One form is low in cancer and high with benign enlargement of the prostate. However, another form is high in cancer. In general, a low percentage of free PSA is worrisome for cancer – but not always. There are some men who have a low free PSA and do not have cancer. We don't know all of the explanations at this time.

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RELATIVELY HIGH PSA BUT LOW CANCER VOLUME: My husband has PSA of 14.7, and Gleason score of 6, but in the biopsy that was done, cancer was found in only 1/200th of the sample tissue. What is likely to explain the high PSA, and yet seemingly small amount of cancer?

Answer: There are several possible explanations. Part of the high PSA could be due to benign prostatic enlargement or inflammation in the prostate. The cancer may be contributing a relatively small proportion of the PSA. Another possibility is that the biopsies may have failed to detect other regions of cancer within the prostate due to simple spatial sampling errors.

HIGH PSA IN OLDER MEN: On an 86 year old male is a PSA score of 10 considered high?

Answer: Yes. A PSA count of 10 is high at any age. It indicates that there is either benign enlargement of the prostate, inflammation in the prostate, prostate cancer - or a combination of the above. It would be prudent to be evaluated by a urologist.

OUTSIDE THINGS THAT AFFECT PSA LEVELS: In a normal, healthy man, would sexual intercourse the morning of the PSA test is performed raise the levels and possibly by how much if at all. Could a prostate exam prior to the PSA test elevate levels and by how much? Could an infection in a healthy man elevate PSA to 21?

Answer: The answer to all three quesitions is yes. Usually, ejaculation or a prostate exam has only a slight effect on the PSA level that lasts for 24 to48 hours only. The PSA might increase a point or two. With infection, very high PSA levels can occur (even up to 21 or higher) and in some cases it takes a long time for the PSA levels to return to baseline. In about 25% of cases, antibiotic therapy is effective; however, some men have to wait for their body’s defense mechanisms to clear the infection.

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RAPIDLY RISING PSA IN PATIENT ON PROSCAR: My 88 yr old father has been on Proscar for 8 yrs now. Last year his PSA count was 4; last week his PSA was 11. The urologist did a digital exam and sonogram. The doctor concluded he had a "substantial" cancerous lesion. The doctor said he will have to do a biopsy to determine the type and stage and whether it is fast or slow growing. The doctor said if fast growing life expectancy can be up to 6 months and if slow growing he may die with it, not from it. I would like your comments in general on the above remarks and the items below.
1. If the doctor feels there are no viable treatments available to slow or prevent lesion spread, is the only reason for a biopsy to give us life expectancy?
2. Does the size of a lesion prohibit radiation, freezing or any other non- surgical remedies?
3. The fact that his PSA count increased from 4 to 11 count in one year, can a reasonable conclusion be made whether this is a fast or slow growing lesion?
3. Would you recommend a second opinion from an oncologist?

Answer: A rising PSA in a patient on Proscar is worrisome for prostate cancer. There are treatments to slow the progression of the cancer. The size limits some treatments, but not radiation or stronger hormonal therapy. If the PSA increase is due only to prostate cancer, it indicates a rapidly growing tumor; however, the increase could also be due, at least in part, to inflammation in the prostate (see other Q&A s on this topic). It never hurts to get another opinion from another urologist, medical oncologist or radiation oncologist.

Can cold or cough medication effect the PSA?

Answer: The only medicines that affect PSA levels are hormones. Medicines that lower male hormones can decrease PSA levels. The only way a cough or cold medication could affect the PSA level would be if it caused urinary retention. Urinary retention can result in a dramatic increase in the PSA levels.

Could very freqent ejaculation cause a constant high PSA level of 16ng/ml?

Answer: I do not believe so. There are probably other causes (benign enlargement of the prostate, inflammation in the prostate, prostate cancer, or combinations of the above). See other questions on the website. Ejaculation usually causes only low-level transient elevations of the PSA level.

Pro-PSA: What are the advantages of the Pro-PSA diagnostic test? If evaluations have been published, please provide citation(s). Where is the test commercially available?

Answer: Pro-PSA is a "new" marker. Preliminary studies indicate that it may be a better marker than free or complexed PSA, but a Pro-PSA test is not available at this time. The test and its results are still in the research stage. Some papers are published on clinical studies using Pro-PSA, and they can be found on the internet in PubMed, a service of the National Library of Medicine, www.pubmed.com. The Fall 2003 issue of Quest had an article on Pro-PSA, “Pro-PSA: Possibly a Better Marker for Prostate Cancer.”

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RISK OF DEVELOPING PROSTATE CANCER? I am 59 years old with PSA of 5.1, a free PSA of 18 percent, a prostate volume of 78, and a negative twelve core biopsy done 6 months ago. Statistically, what is my risk of developing cancer that should be treated?
Answer: It is possible that a 12-core biopsy could have missed a prostate cancer, so you cannot be 100% certain that there is no prostate cancer. You should continue to be followed with PSA testing and digital rectal examination and consider repeating the biopsy if either test becomes more abnormal. There might be as high as a 15% to 20% chance that you could be diagnosed with prostate cancer in the relatively near future, in my opinion.

GLEASON GRADE 2+2: Should I have a second pathology report to verify prostate cancer is actually present with these very low numbers?

Answer: Yes. In recent years, it is very uncommon for pathologists to score prostate cancer in the low end of the Gleason scoring range (less than Gleason sums of 5). It is always a good idea to have slides reviewed, and especially so in this case.

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ELDERLY MAN WITH VERY HIGH PSA: My dad is 89 and his PSA level has increased to 96. Does this mean he has terminal cancer? He does not want a biopsy as the urologist says they can do nothing for him. He has no pain.

Answer: In my opinion, he almost certainly has advanced prostate cancer. If it does cause symptoms, it is very likely that he could be successfully treated with hormonal therapy. If he does not wish to have a biopsy, he should be monitored closely by an experienced urologist who would be prepared to intervene appropriately.

PSA ANXIETY: I am a 56 year old man with a persistently rising PSA that sometimes comes down with antibiotic therapy. I have had multiple biopsies that have shown atypical cells and PIN but no cancer. Needless to say I am still worried. Is there anything else that I can do?

Answer: In my opinion, nothing but to continue to watch the PSA carefully and to be willing to have more biopsies if the PSA rises further. Biopsies in the anterior and the central regions of the prostate are especially important in cases such as yours.

WHAT ORGANS PRODUCE MALE HORMONES? I was told that the PSA readings could be affected by testosterone production in the testicles and another organ? What is the name of that organ.

Answer: The adrenal glands normally produce male hormones in relatively small quantities that can affect PSA levels. In fact, some treatments for advanced prostate cancer, such as keotconazole probably lower PSA levels by eliminating the production of male hormones by the adrenal glands.

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CANCER OR PROSTATITIS? I am 43 yrs old and recently had a PSA concentration of 4.9. My doctor said the digital examination suggested that the prostrate felt slightly enlarged but smooth. He has put me on a course of antibiotics. Is my condition more likely to be cancer or some form of prostatis?

Answer: I is more likely to be prostatitis because of your young age, but it could be cancer - especially if you have a family history of early age at onset prostate cancer. If the PSA does not decrease below 2.5 with the antibiotics, I would recommend that you have a biopsy.

PSA REPEATEDLY IN CONCERNED ZONE: What should a man do if he has had repeated negative biopsies but his PSA test is in the concerned zone? I have had six biopsy procedures, initiated with PSA's from 8-19, and all have been negative.

Answer: Many men have a high PSA because of benign enlargement and/or inflammation and do not have cancer. The odds are that you are one of these men. It is important to stay under the care of a urologist and make sure you go in for scheduled tests and check-ups. These may include repeated biopsy sessions, especially if the PSA continues to rise, as biopsies are only small samples of the prostate gland, and it is not infrequent that initial biopsies miss the cancer.

TESTOSTERONE THERAPY AND PSA: Could taking a testosterone enhancing product give you an elevated PSA reading?

Answer: It could if your testosterone level was low to start with (as it presumably was) and therefore was masking your true PSA level. If the PSA is high, you should consider a prostate biopsy

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I am a 37 year old man who was treated over a year ago for testaliga. I recently had my yearly physical exam and my PSA was 3.9 and the DRE results showed a slightly enlarged prostate which, according to my doctor, was prostatitis. I was told to see my urologist and be given a bladder ultrasound and DRE. I was put on medication for a month and retested after a month and my PSA dropped to 2.9. My urologist told me that this was good news and that I should return in one year to be re-examined. Should I be worried that a biopsy was not done at this time?

Answer: In my opinion, a PSA of 2.9 is too high. I would continue to monitor the PSA quarterly, and, if it does not continue to decrease, would recommend a biopsy.

My urologist did not recommend a biopsy after my original PSA test results were 3.9. He first recommended medication therapy and after a month I was retested and my PSA had dropped to 2.9. I see in your Q&A section that you routinely recommend biopsy to those who have PSA of 2.5 or higher. I am a 37 year old man who is worried about what I should do? Right now I know my latest reading was 2.9 . Why would my urologist go this route and you suggest something entirely different? Should I wait a year as my urologist suggested and have my PSA, DRE test done again at that time or should I seek a second opinion?
At age 37, the most likely cause of your PSA elevation is prostatitis. It is further supported by the fact that your PSA level came down. However, at age 37, a PSA of 2.9 is high, and I would monitor the PSA more frequently - say every three months for a while. If it does not go down to below 1, I would suggest that you consider a biopsy.

Does alcohol affect the PSA score?

Answer: No.

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DOES GOUT OR ITS TREATMENT AFFECT PSA LEVELS? In 1999, my PSA jumped from 3.1 to 6.6. Antibiotics reduced my reading to 4.5. It has fluctuated between 4.5 and 5.5 in the last four years, until this week, when it jumped to 16. I have an enlarged prostate, which results in some urine retention. I have gout and take medicine for it to reduce my uric acid. The day before the PSA test I had such a bout. Could that have affected these results?

Answer: Not to my knowledge. Neither gout or the medications used to treat it affect PSA levels. The most common cause of a fluctuating PSA level is inflammation in the prostate gland, but it is possible also to have benign enlargement and cancer. I would advise another course of antibiotics, and if the PSA does not return to baseline, I would advise a prostate biopsy.

Q: FLUCTUATING PSA RESULTS: What would make a man's PSA go from 4.8 to 9.l then back to 5.4 and back to up to l0.9. His digital rectal exam was normal.

Answer: Inflammation in the prostate, also called prostatitis. However, remember that a PSA of 4.8 and 5.4 is high and it is possible to have both prostatitis and prostate cancer. If the PSA does not decrease to below 2.5, I would recommend that you have a prostate biopsy. Please see other Q&As on my website referring to fluctuating PSA levels.

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I am really confused. I’m 59 years old and in excellent health. My PSA rose 3.4 to 5.9 in two years. Free psa 8.0%. DRE (2) Normal. 10 sample biopsy normal. My urologist said to come back in 6 months. I have increased frequency of urination and decreased flow which have gradually worsened beginning around age 47. Not severe but annoying. What's your opinion?

Answer: I would recommend asking your urologist to culture your urine and try a 4 to 6 week course of antibiotics, such as Cipro 500 mg twice a day, to see if that has a beneficial effect on your symptoms and PSA level. Your urologist might want to check your urine for abnormal cells with a cytology test and might want to perform cystoscopy to ensure that everything looks alright on the inside. It might be necessary to repeat the biopsy procedure in the future.

Are we sure that high PSA is an indication of prostate cancer? Could some substances, food or other trigger the PSA level?

Answer: A high PSA does not always mean cancer. It can be caused by an enlarged prostate gland, inflammation in the prostate gland, or other benign conditions. However, the higher the PSA, the greater the likelihood that prostate cancer is present.

TESTOSTERONE AND PSA LEVELS: Can taking testosterone raise a mans PSA levels? And if so why? If a man is taking it to bring his hormone levels back to normal or close to normal, why would it?

Answer: It can raise PSA levels if the PSA levels were suppressed because of the low testosterone level, which often is the case when the testosterone level is low enough to warrant treatment. However, if the testosterone levels are not abnormally low, giving additional testosterone might not increase the PSA levels.

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Pro-PSA: What are the proPSA guidelines for recommending biopsies for men with PSAscores of 2.0-4.0?

Answer: Pro-PSA is not yet available for clinical use. No guidelines have been established at this time.

My father just died from aggressive prostate cancer. He was 59. I am 33. When should I get checked?

Answer: You could start at once and get a baseline PSA and digital rectal examination, and, in my opinion, it would not hurt to repeat it annually. In any case, I would not recommend waiting until after age 40.

YOUNG AND CAP FAMILY HISTORY: How often should a 45 year old male get a PSA with a family history of prostate cancer?

Answer: At least annually, and, in my opinion, every 6 months would not be too often. A 45 year old’s PSA should be less than 1.0 ng/ml at age 45. If it is higher, I would advise a course of antibiotics and if the PSA did not decrease to lower than 1, I would advise considering a biopsy.

What is your advice for a 45 year old white male with PSA of 1.56 Two brothers have prostate cancer and my father died from prostate cancer. What do you recommend for further evaluation and follow up?

Answer: The median PSA value for men in their 40s is about 0.6 ng/ml. If the PSA is higher, there is a higher risk of being diagnosed with prostate cancer. I would advise you to try a course of antibiotics and if the PSA did not decrease to lower than 1, I would advise you to consider having a biopsy. If you do not have a biopsy, you should follow your PSA very closely.

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I am a 52 year old white male. I have prostate cancer history in the family: my father and two older brothers – one aged 54 years and the second 53 years at their time of diagnosis. My PSA is now 1.97. At 51, it was 2.8; at 50 it was 1.8; at 49 it was 2.0. I am now taking 200 mcg of selenium and having my PSA measured at 6 month intervals. Am I doing enough?

Answer: Your PSA is a little bit higher than that of the usual 52 year-old man (median PSA 0.6-0.9). With your family history, I would advise you to continue to follow it carefully and if it trends upward at all, I would recommend that you consider having a biopsy.

RISING PSA IN THE LOW RANGE: I'm 53 years old. In the past three years of annual testing, my PSA went from: 1.83 to 2.04 to 2.78. Is this rising too fast?

Answer: In my opinion, yes. I would advise you to have a biopsy.

DECREASING FREE PSA: Would a declining prostate volume result in one's free PSA value to decline also - even if there was no prostate cancer? My thinking is that whatever was earlier shown as bound in larger prostate gland would continue to be there, but inside a much smaller environment - thus possibly causing one's free PSA reading to decline. Does this make sense or just what is the situation?

Answer: It could. We now know that "free" PSA is made up of several components: BPSA and IPSA that are increased with benign prostatic enlargement (BPH) and proPSA that is increased with cancer. So, if the prostate shrinks because of treatment of BPH, the free PSA level could decrease.

AVODART'S EFFECT ON PSA: Taking Avodart three months PSA 4.5 What is the true reading?

Answer: It is hard to say, but certainly higher, and high enough to recommend a biopsy.

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PSA VELOCITY AND WATCHFUL WAITING: I read your article on PSA velocity and morbidity in the July 8 NEJM and wondered if it might mean that watchful waiting might be a plausible option for me, particularly considering the lifestyle impacts of both RP and radiation? In April 2004, I had a positive biopsy (left lobe: 30% of one biopsy core, moderately differentiated, Gleason 6 (3+3); right lobe: 5% of one biopsy core, focal moderately differentiated, Gleason 6 (3+3)--perineural invasion not detected). My PSA scores have been: March 01: 3.5 Sept. 02: 3.9Mar. 03: 3.5Oct. 03: 4.2Feb. 04: 4.2 (free ratio 8.1%)May 04: 8.6July 04: 4.7I am a 54 year old man, otherwise in seemingly good health.

Answer: Although your tumor features and PSA velocity are favorable, I would not recommend watchful waiting because of your young age. Your prostate cancer will have a long time to progress, if you are otherwise healthy, and the earlier you have it treated, the better, in my opinion.

WHAT IS A HIGH PSA? What is considered high from a PSA report or what is the range of PSA readings in the blood stream?

Answer: The range is from 0 to thousands. In men with a perfectly healthy prostate gland (i.e., no benign enlargement, no inflammation, no cancer) the PSA should be less than 1. Any of these conditions can raise the PSA level. However, there is a direct association between the PSA level and the risk of cancer. It is about 10% to 15% if the PSA is less than 2.5; about 25% if the PSA is 2.6 to 4; about 35% to 40% if the PSA is 4-10; and more than 50% if the PSA is higher than 10. See the Quest article of August 2004 for more recent information on other PSA measures such as PSA velocity, PSA density, Pprcent free or complexed PSA, etc.

I've read your Q&As regarding infection in the prostate and its effect on PSA, but can infections other places in the body affect the PSA. Specifically, I'd like to know about periodontal or gum infection and its possible effect on PSA.

Answer: They have no effect on the PSA level. Only urinary tract and prostate infections affect the PSA.

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My PSA has been steady for about two years at 7.5. But my free PSA is at 6%, having started at 14%. Biopsies two years ago found 10 suspicious cells. Our urologist suggested more tests in a few months. Should we be worried.

Answer: If the suspicious cells were high-grade PIN (prostatic intraepithelia neoplasia) or ASAP (atypical small acinar proliferation), and the percent free PSA is decreasing to 6%, I would be concerned. However, it is reassuring that his total PSA has not increased for the past two years. Perhaps, the safest course would be to repeat the biopsy procedure. If you do not wish to do this, I would recommend that the PSA levels be measured every 3 to 6 months.

Can medicines for cholesterol and for heart problems cause a rise in PSA? Also, can these medications cause a rise in PSA after a radical prostatectomy, and would they have any adverse interactions with hormonal therapy treatments?

Answer: No. In fact, emerging evidence suggests that medications for cholesterol (statins) might lower the risk for prostate cancer and might decrease the aggressiveness of prostate cancer.

Is there any connection between using Viagra and PSA values?

Answer: No, there isn’t.

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Should a family history of prostate cancer affect the total PSA or PSA Velocity threshold for biopsy?

Answer: Men with a family history of prostate cancer are often biopsied at a younger age– due to an elevated PSA – than men without a family history of prostate cancer.

Men with a family history of prostate cancer are diagnosed with prostate cancer at a younger age than men without a family history of prostate cancer.

A family history of prostate cancer appears to be associated with a higher rate of cancer diagnosis among men with a total PSA level from 2.5 to 4.0 ng/ml or a PSA Velocity of more than 0.75 mg/ml in a year.

Although family history of prostate cancer is associated with an increased risk of cancer diagnosis, it is not associated with more aggressive tumor features.

(taken from a URF sponsored study presented at the May, 2008 AUA meeting)

 I am 53 years old and taking Flomax. My PSA test was 14.9 and three weeks later, it was 12.0. My DRE was clean. My primary physician told me that a high PSA doesn’t necessarily indicate prostate cancer? Why would he say that? And is there any truth to it?

Answer: There is truth to the fact that not everyone with a high PSA value has prostate cancer, especially if the PSA decreases spontaneously or in response to antibiotic treatment.

However, the median PSA value for men in their 50s is less than 1 (0.9), and the higher the PSA is above that value, the more likely they have prostate cancer.

If your PSA does not decrease dramatically, I would recommend a biopsy.

4.1

Karl Loren's Treatment Protocol

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Ph Flush™

Formula Created by Karl Loren, four capsules per day, spread evenly, provide a total of:

Germanium -- Pure Powder 2 grams per day

Taheebo Life Tea -- pure powder, equivalent of 40 capsules per day

Selenium -- 400 mcg per day

Pycnogenol -- Form and amount as created by Clifford Woods

Alkaline Water and Regular pH testing to ensure drinking of 8.0 water and body fluids maintaining steady alkaline state.

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9.9

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Vital Statistics

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Date/Time Weight Fat % Muscle RestMetab BMI VisFat Blood Pressure

07.17.09:10:30 AM
Doctor's Office
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            130/xxx Pulse 74
07.19.09:1:25 PM 252.6 27.3 31.3 2086 41.1 29 159.88L87
07.20.09: 8:00 AM 252.0 29.4 30.4 2885 41.0 29 178/92 Pulse 75 3:18 AM
07.21.09 AM 253.2 30.1 30.0 2093 41.2 29 190/109 Pulse: 67 4:08 /AM
(very cold roon)
07.24.09 AM 253.4 30.1   2093 41.1 29

179/84 Pulse 91 /AM
(right after sauna)

             
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eMail Exchanges With Subscribers

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Date/Reference Click on Message Reference for the message
References

Jim, started on 07.20.09
Mike, started on 07.21.09

 

 

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Jim: Started on 07.20.09

Received 7.20.09

Message_Text:

Dear Karl,

I am a 71 year old 205 # white male with a 130 gram prostate. My psa has been from 4.5 to as high as 23. for the last couple of years

it has been 5 to 7 while taking uroxatrol and avodart.

Had a biopsy 1998 and mris 2 years ago both negative.

I would very much like to get off the meds but am afraid of not being able to urinate when on a camp or hunt trip as well as getting up 5 to 8 times a night and not get a good nights sleep.

Any thoughts or suggestions greatly appreciated.

Thank you kindly. Jim

Response from Karl on 07.20.09

Dear Jim,

Your last name is familiar. Have we had contact in the past?

It happens that I have a considerable interest in PSA and prostate since, less than a week ago I got my first "high" PSA score -- it was 15. I am 78, used to hike a great deal when I was a youngster like you.

I immediately started a new web page, this one, on which I am publishing my research and personal treatment protocol.

I weigh more than you -- I need a sleep Apnea mask to get a good night's sleep -- also greatly reduces the need to urinate during the night. I usually only get up once, maybe 4 AM, and often just stay up then to do some work on one of my web sites. I also get in my pool exercise and sauna every day, usually 7 days per week.

I often do this -- publish some personal health problem BEFORE I have solved it, then work on the solution, all the while publishing my results on a daily basis.

I also, generally, publicize the web page I use, and encourage you to subscribe to my Premium Edition of the Dark Times Digest (can be done here) and exchange messages with me, personally.

I will not publish any of your personal information unless you authorize it, but I will publish our exchange of messages as long as they seem of interest to my viewing public.

However, if you are willing I would love to put your picture here and any other personal information you are willing to share. One of my favorite photos is here.

As you can see I'm a Kung Fu student -- started when I was 74. I have an earned Orange Belt and an honorary Black Belt from my Kung Fu School' where I am the school webmaster and photographer. I have published thousands of my photos on that site.

The other image is of me and my wife, practicing Kung Fu Stick Fighting right in front of the small pool I use for daily exercise. That's my dog Scotty on the left in the photo.

Here is me in the pool doing Kung Fu punches:

So, this web page is my first suggestion that you look over -- particularly the two very personal "notes" I've written about my own PSA and prostate cancer situation: Note1 and Note 2.

You can also browse through any or none or all of the pages on that Web Site -- this is where I publish my Dark Times Digests.

Let me know what you think of all this?

Thanks,

Karl Loren.

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Mike: 07.21.09

Received 7.21.09

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Hi Karl,

I'm new to your site but in the last 24 hrs I've read an awful lot and I've actually asked questions regarding some personal issues I'm dealing with and received a polite email back from an assistant.

The information did not teach me anything new about hypothyroidism but it would be fair to say I have really educated myself on the subject.

Unfortunately, it was the day after my wife had a CT scan that the red flags started coming up all over the place about the dangers in these scans.

Turns out 65% of people who have this particular scan perform fall victim to thyroid cancer within 10 years.

I'm off topic a little here, the point of this letter relates to some of the advice you were giving young parents who have autistic children. You seems certain that pre natal issues play a large role, perhaps you are not aware as government in Canada and the US are purposefully delaying and appealing court decisions on the matter but I can tell you with confidence that the MMR vaccine (measles, mumps and rubella) is the likely cause of autism.

You are right about mercury playing the role which makes this whole topic quite sickening. Why would vaccine manufacturers put mercury, lead and in some cases fluoride in vaccines. A typical case of big pharma wanting a sick population.

On another note, you very rarely ever mention the effects that water fluoridation has had and remains having on our population. Fluoride is most certainly the cause of ADD and ADHD and in fact, new declassified information tells us that fluoride is not only responsible for the reduced IQ of children but there is a direct correlation between cities with fluoridated water having significantly higher levels of cancer, especially bone, thyroid and blood cancers. Hopefully you'll find out more than I have and you will offer some much needed advise on how we can rid our bodies of the accumulated fluoride which stays trapped in our thyroid and also stores itself in our bones. Check out the facts, they are absolutely appalling, it is a wonder the establishment has not faced any class action lawsuits.

Thanks for listening

Mike

Karl's Response on 07.21.09

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Dear Mike,

I may well be doing more than listening.

I have two quite separate thoughts for you.

First, what you write can well be a new research project for "us" to include you, me and my Executive Director, Clifford Woods.

Second, there IS an explanation of how and why this is happening and that subject has become my personal mission, now at the age of 78 and "seeing" very clearly what is happening on the planet.

I urge you to spend some HOURS reading THIS page -- the background of my not--finished Dark Times Digest Newsletter (which, eventually, will be published here). These links deal with the US FDA, but more fundamentally, with the horror which is engulfing our world -- not accidental -- but deliberate destruction of health and Western values. You'll be a bit shocked at the truth I'm revealing. It would be great, too, if you subscribe to my Premium Edition of the Dark Times Digest HERE.

I have written a lot about autism, and would enjoy exchanging with you -- since I wrote about that subject many years ago. Also, I'm busy with some special projects of my own and think that my Executive Director, Clifford Woods, can help here.

I'll send you the link to THIS page, invite your careful study of the links I've given above, and then your further comments.

Kind Regards,

Karl Loren

Mike's Response, Received 07.23.09:

Hi Karl,

I appreciate you getting back to me so quickly. I have started reading the material you included in your reply. It is fascinating how inherently corrupt the establishment really is.

Karl, be prepared to have your socks blown off. I have included a link to a blog, an interview done in France of a Canadian doctor who is the undisputed pioneer and leader in his field. His conclusive findings, if and when they ever hit mainstream, are sure to change the landscape of medicine forever.

I won't carry on any farther, the interview really says it all.

Let me know what you think.

Mike

http://censored31.skynetblogs.be/

Karl's further response on 07.23.09

Dear Mike,

I did visit the web site you suggested.

This man may have the magic to turn lead into gold, but he is NOT credible for reasons that may offend you.

My own research and writings on heart disease and cancer are NOT less revolutionary than his stuff, but HE has to tell his story down in some dark alley.

I have labored these 35 years, always very much in the public spotlight. I have not only done the revolutionary research, but published it on more than 100,000 web pages.

Any fool can write and if he learns how and has the money, any fool can publish thousands of pages of junk.MOST of what I find IS JUNK .I do not write such.

It is too bad, perhaps, that good ideas don't, somehow, get found easily. Not so, I have worked hard these 35 years to get my stuff into the MAIN STREAM. The best measure of a web site is "page visits" == one person visits on page at one date/time. That is "one page visit." I have gotten over 300,000 page visits on my thousands of pages EVERY MONTH, and that indicates that thousands of people are reading my stuff.

Next, I put my money where my mouth is. I've designed formulas that save lives. I sell millions of dollars of this stuff, and have many customers who have bought regularly from me for more than 10 years.

I am not modest about it, but there just isn't any other person in the world who comes close to me in accomplishment.

Why am I not BETTER KNOWN? That is the subject of my new research and writing. THERE IS suppression on our planet -- suppression of bright good ideas. Millions of people have succumbed to those evil intentions -- and voted for Obama. I have, somehow, stayed free of those influences and prospered. The whole of my story is published and one place where you can get a taste of ME, is HERE, but do not think to brag to me, and urge me to look, about some obscure doctor who has not succeeded in the face of evil.

Mike, your English sets you apart from the crowd, but you need to spend some hundreds of hours on my web sites if you want to live through these coming Dark Times and achieve "heaven"

Karl Loren

Mike's Response 07.23.09:Later, same day

On Thu, Jul 23, 2009 at 11:28 AM, Mike Roy <mikeroy23@gmail.com> wrote:

Hi Karl,
I appreciate your candor and will commit to validating anything I might send you in the future. My immediate response will be to bury my head and thoughts into studying your pages. It certainly wasn't my intention to offend you.

Regards,

Mike

Dear Mike,

An author without a reader is a thirsty man in a desert.

You do not offend me.

You are obviously a well - educated person.

I am eager to get through to more people about what I consider is a greater threat, by far, to our Nation, than the Obama Health Care Bill.

I am certain about my data, but not yet certain how to write about my reality so as to INTEREST others -- interest comes first, then convince.

So, indeed, bury your head and then let me have a "stranger/reader's" viewpoint of whatever happend?

That would be great.

but, you've not yet told me about yourself and your interests?

Karl Loren

 

 

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