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Hi Chuck,

I have read all your responses to my proscar/avodart questions.

I was just wondering what your thoughts were. My husband was diagnosed in March,

2010 with PSA of 7.5 and GS 4+3. He has no symptoms. After doing research

(mainly through me), he decided that he didn't like any side effects and has

decided to bide his time. Through diet and supplements, his PSA has dropped to

6.5. So, he is planning on waiting till a rise in his psa before he gets radical

treatment.

I know that there are no studies on how this affects men who aren't doing any

other treatment, but I do know that all the studies shows that these drugs may

slow down cancer growth. It is used for men to lengthen ADT holiday length after

failed surgery. Plus, of course, studies showed that there was less cancer in

men who took the drugs (which indicates to me that it is slowing down growth,

not stopping cancer)

In the mean time, since he doesn't want any radical treatment, we were thinking,

what can it hurt to try finisteride/dusteride? If he doesn't like the side

effects, he can stop.

We are aware that it would reset his psa for a new baseline, and if it changed

from whatever the new number is, then he will have to do something. We are also

aware that it makes it easier to see higher grade cancers, so that is not

necessarily a bad thing.

Please let me know if you have any thoughts on this. Our VA urologist wouldn't

discuss the matter with us as he only wanted my husband to have treatment.

Thank you for your time,

Lynn

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Hi, you said :- > We are also aware that it makes it easier to see higher grade cancers, so that is not necessarily a bad thingI would argue it is possibly a bad thing. There is a danger of higher grade cancers being provoked by the treatment, for example:-

In

1998 researchers comparing finasteride to placebo observed that

finasteride reduced benign prostate growth with .. a decrease in

PSA of 48% ..

But

look at the catch: of that finasteride treated group 30%

had prostate cancer at the end of a twelve month trial. Whereas

in the observation group (no finasteride treatment) one

cancer in all was detected i.

This

early finasteride trial anticipated the 2003 outcome of the much

larger Prostate Cancer Prevention Trial (PCPT)

which was abandoned, it now appears, for safety reasons. Both finasteride and dutasteride have been associated with suppressing

PSA and reducing prostate volume. This may be advantageous for simple

cases of BPH that do not have latent lesions or a malfunctioning

estrogen receptor due to fetal developmental estrogenization (see

articles section 5). The 5-alpha reductase inhibitors finasteride and

dutasteride were designed to prevent the conversion of testosterone

to DHT and so inhibit prostate growth and reduce PSA expression.

Combined with an alpha-adrenoceptor blocker such as tamsulosin,

efficient management of simple BPH may be obtained. However, reducing

stromal prostate volume with 5αRI drugs

may not have a good outcome where there is latent prostate cancer,

because growth control factors, including PSA, originate in the

stromaii.

Since BPH is neither the same as, or a precursor per se to

carcinoma, the reduction of both BPH and subsequent PSA output

achieved by 5αRI medications is

unnecessary. More importantly however, removal of antiangiogenic

components of PSA from the scene may trigger latent carcinoma to

enter a more active phase that we see reflected in the increased

number of higher grade carcinomas in 5αRI

treated groups compared to placebo. Simply lowering PSA in this

scenario is a false reassurance.

i

Cote RJ, Skinner EC, Salem CE, Mertes SJ, Stanczyk FZ, BE,

Pike MC, Ross RK. The effect of finasteride on the prostate

gland in men with elevated serum prostate-specific antigen levels.

Br J Cancer. 1998 Aug;78(3):413-8. PubMed:9703292

ii

Briganti A, Chun FK, Suardi N, Gallina A, Walz J, Graefen M, Shariat

S, Ebersdobler A, Rigatti P, Perrotte P, Saad F, Montorsi F, Huland

H, Karakiewicz PI. Prostate volume and adverse prostate cancer

features: fact not artifact. Eur J Cancer. 2007

Dec;43(18):2669-77. PubMed:17996442

-- Sam.

http://fitcare.org.uk/epidemic/4.2.chemoprevention.update.html--- In ProstateCancerSupport , "LYNN" wrote:>> Hi Chuck,> > I have read all your responses to my proscar/avodart questions.> > I was just wondering what your thoughts were. My husband was diagnosed in March, 2010 with PSA of 7.5 and GS 4+3. He has no symptoms. After doing research (mainly through me), he decided that he didn't like any side effects and has decided to bide his time. Through diet and supplements, his PSA has dropped to 6.5. So, he is planning on waiting till a rise in his psa before he gets radical treatment.> > I know that there are no studies on how this affects men who aren't doing any other treatment, but I do know that all the studies shows that these drugs may slow down cancer growth. It is used for men to lengthen ADT holiday length after failed surgery. Plus, of course, studies showed that there was less cancer in men who took the drugs (which indicates to me that it is slowing down growth, not stopping cancer)> > In the mean time, since he doesn't want any radical treatment, we were thinking, what can it hurt to try finisteride/dusteride? If he doesn't like the side effects, he can stop. > > We are aware that it would reset his psa for a new baseline, and if it changed from whatever the new number is, then he will have to do something. We are also aware that it makes it easier to see higher grade cancers, so that is not necessarily a bad thing.> > Please let me know if you have any thoughts on this. Our VA urologist wouldn't discuss the matter with us as he only wanted my husband to have treatment.> > Thank you for your time,> Lynn>

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Hi, you said :- > We are also aware that it makes it easier to see higher grade cancers, so that is not necessarily a bad thingI would argue it is possibly a bad thing. There is a danger of higher grade cancers being provoked by the treatment, for example:-

In

1998 researchers comparing finasteride to placebo observed that

finasteride reduced benign prostate growth with .. a decrease in

PSA of 48% ..

But

look at the catch: of that finasteride treated group 30%

had prostate cancer at the end of a twelve month trial. Whereas

in the observation group (no finasteride treatment) one

cancer in all was detected i.

This

early finasteride trial anticipated the 2003 outcome of the much

larger Prostate Cancer Prevention Trial (PCPT)

which was abandoned, it now appears, for safety reasons. Both finasteride and dutasteride have been associated with suppressing

PSA and reducing prostate volume. This may be advantageous for simple

cases of BPH that do not have latent lesions or a malfunctioning

estrogen receptor due to fetal developmental estrogenization (see

articles section 5). The 5-alpha reductase inhibitors finasteride and

dutasteride were designed to prevent the conversion of testosterone

to DHT and so inhibit prostate growth and reduce PSA expression.

Combined with an alpha-adrenoceptor blocker such as tamsulosin,

efficient management of simple BPH may be obtained. However, reducing

stromal prostate volume with 5αRI drugs

may not have a good outcome where there is latent prostate cancer,

because growth control factors, including PSA, originate in the

stromaii.

Since BPH is neither the same as, or a precursor per se to

carcinoma, the reduction of both BPH and subsequent PSA output

achieved by 5αRI medications is

unnecessary. More importantly however, removal of antiangiogenic

components of PSA from the scene may trigger latent carcinoma to

enter a more active phase that we see reflected in the increased

number of higher grade carcinomas in 5αRI

treated groups compared to placebo. Simply lowering PSA in this

scenario is a false reassurance.

i

Cote RJ, Skinner EC, Salem CE, Mertes SJ, Stanczyk FZ, BE,

Pike MC, Ross RK. The effect of finasteride on the prostate

gland in men with elevated serum prostate-specific antigen levels.

Br J Cancer. 1998 Aug;78(3):413-8. PubMed:9703292

ii

Briganti A, Chun FK, Suardi N, Gallina A, Walz J, Graefen M, Shariat

S, Ebersdobler A, Rigatti P, Perrotte P, Saad F, Montorsi F, Huland

H, Karakiewicz PI. Prostate volume and adverse prostate cancer

features: fact not artifact. Eur J Cancer. 2007

Dec;43(18):2669-77. PubMed:17996442

-- Sam.

http://fitcare.org.uk/epidemic/4.2.chemoprevention.update.html--- In ProstateCancerSupport , "LYNN" wrote:>> Hi Chuck,> > I have read all your responses to my proscar/avodart questions.> > I was just wondering what your thoughts were. My husband was diagnosed in March, 2010 with PSA of 7.5 and GS 4+3. He has no symptoms. After doing research (mainly through me), he decided that he didn't like any side effects and has decided to bide his time. Through diet and supplements, his PSA has dropped to 6.5. So, he is planning on waiting till a rise in his psa before he gets radical treatment.> > I know that there are no studies on how this affects men who aren't doing any other treatment, but I do know that all the studies shows that these drugs may slow down cancer growth. It is used for men to lengthen ADT holiday length after failed surgery. Plus, of course, studies showed that there was less cancer in men who took the drugs (which indicates to me that it is slowing down growth, not stopping cancer)> > In the mean time, since he doesn't want any radical treatment, we were thinking, what can it hurt to try finisteride/dusteride? If he doesn't like the side effects, he can stop. > > We are aware that it would reset his psa for a new baseline, and if it changed from whatever the new number is, then he will have to do something. We are also aware that it makes it easier to see higher grade cancers, so that is not necessarily a bad thing.> > Please let me know if you have any thoughts on this. Our VA urologist wouldn't discuss the matter with us as he only wanted my husband to have treatment.> > Thank you for your time,> Lynn>

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