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Medical Forum / Diseases and Disorders / Prostate Cancer / November 2004

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TINKPOTDUDE II - 31 Oct 2004 18:48 GMT
I have been diagnosed with very little prostate cancer.  Out of 14
snippets taken during my biopsy, only one showed a trace of just 5%.

I refuse to have the prostatectomy!  However, I have heard wonderful
things about the freezing procedure.

Will some of you be good enough to let me hear from you via email about
this method?  I understand it only kills the cancer cells.

Thank you for your help in this matter.

Edward
Danny McCarty - 31 Oct 2004 19:04 GMT
>Subject: QUESTION
>From: MRROTHROCK@webtv.net  (TINKPOTDUDE II)
[quoted text clipped - 13 lines]
>
>Edward

You left out the other important item- what was the Gleason score.
Persons with serious prostate cancer widespread in the prostate frequently have
a totally negative biopsy.  Your single core with "only" 5% does NOT mean that
the cancer is minor.
Regardless of the method of doing it, the entire prostate MUST be removed or
killed.  The choice of method- RRP, radiation, cryo, whatever, is based on
efficacy and aftereffects like impotence and incontinence.  Read more of this
newsgroup, read the Phoenix site, read books.  Forget about your sex life for a
while.  Please.
Nevertheless, I wish you good luck.  
Stephen Jordan - 31 Oct 2004 21:22 GMT
Quoting Edward:

>>I have been diagnosed with very little prostate cancer.  Out of 14
>>snippets taken during my biopsy, only one showed a trace of just 5%.
[quoted text clipped - 4 lines]
>>Will some of you be good enough to let me hear from you via email about
>>this method?  I understand it only kills the cancer cells.

Danny replied:

> You left out the other important item- what was the Gleason score.
> Persons with serious prostate cancer widespread in the prostate frequently have
[quoted text clipped - 5 lines]
> newsgroup, read the Phoenix site, read books.  Forget about your sex life for a
> while.  Please.

Danny is absolutely correct about the Gleason grade of the
sample, and the fact that it's a tiny sample at best.

Other important -- no, *vital* --  factors are:

1. The TNM score.
2. The PSA score.
3. If "free PSA" and/or PAP (prostatic acid phosphatase) were
checked, what result?
4. Edward's age and general health.

Edward is entering into a phase of his life in which PCa very
well may be a factor as long as he lives. The earlier he begins
the struggle, the better are the prospects for good results. And
good results often mean simple survival, not necessarily "cure,"
however it's defined (and there are differences on that point).

As for cryotherapy: Based upon a Gleason 9 score (4+5, 6 of 7
cores, right side), T2bN0M0 (palpable tumor, no lymph node
involvement nor metastases), PSA 4.75 diagnosis, at age 67 (good
health, otherwise) I underwent cryosurgery on November 20, 2003.

I am not pleased with the result.

Due to rising PSA observed post-procedure, a second biopsy was
performed on July 20, 2004. It disclosed that the Gleason 9 tumor
was evidently destroyed by the cryo, BUT one of six cores
disclosed a Gleason 8 (4+4) tumor at the left base. The
urologist's explanation: "we missed it." Swell.

Side effects: IIRC, cryo results in impotence for some 80% of
patients. There is a period of time when a catheter must be used
to drain the bladder. In my case, it was a suprapubic catheter
through the lower abdomen, though a Foley (through the urethra)
might be used, instead. I'm a slow healer, and it took a month
before it could be removed. Then, the catheter wound leaked for a
couple of weeks while it healed. Fortunately, it was not a
constant leakage; only when I urinated. Had to wear a gauze pad,
though. Yech.

And, yes, I'm impotent.

I have now just completed a course of high-dose radiotherapy
known as Intensity Modulated Radiotherapy (IMRT), and presently
am on androgen deprivation therapy (ADT). This from an oncologist
recommended by the uro, who it seems gave up on me.

Whether any of this will have a good result remains to be seen.
As my onc says, we're going to be together "forever." At the
beginning, he told me frankly that he had no idea how this would
go, as the cryo "threw a monkey wrench" into his evaluation. So
far, though, he's pleased. I hardly need say that I am, too. But
it remains to be seen whether it worked as desired. He has one
other patient who is in much the same situation, though his new
tumor did not manifest itself for over a year post-cryo. For
privacy reasons, the onc cannot discuss that patient with me, and
the patient did not respond to a phone message I left about a
month ago. Reason: unknown.

Regarding invasiveness, I'd place cryo between radical
prostatectomy and IMRT (most-invasive --> least invasive).

Each modality has its benefits and its risks. Edward has a choice
to make and I recommend that, unlike me, he not be stampeded.
Study the various treatments (which include "watchful waiting")
and select that in which he places the most confidence. Also: do
not be afraid to ask exhaustive questions of his physician. Check
the various news groups. Go to ustoo.com and explore. He's
probably got time to do research.

If he does so, he'll probably be comfortable with whatever
decision he makes.

Meanwhile, if he'll supply the info requested above, I'll try to
be helpful. So will others. This is a fine group.

Regards,

Steve J
__
And, most importantly,

"Never give in--never, never, never, never, in nothing great or
small, large or petty, never give in except to convictions of
honour and good sense. Never yield to force; never yield to the
apparently overwhelming might of the enemy.''
--Sir Winston Leonard Spencer Churchill
hankmackxxxx@usa.net - 31 Oct 2004 23:00 GMT
Don't be too hasty  to rule either in or out any particular treatment.  PC
can be a killer.  Read Dr Walsh's book, get several opinions, make a
decision and go for it.  You will find this newsgroup very helpfull.  Good
luck.
,
Leonard Evens - 01 Nov 2004 02:35 GMT
> I have been diagnosed with very little prostate cancer.  Out of 14
> snippets taken during my biopsy, only one showed a trace of just 5%.
>
> I refuse to have the prostatectomy!  However, I have heard wonderful
> things about the freezing procedure.

Cryosurgery does not have a very good track record in the treatment of
prostate cancer.

As others have noted, some more information might help us understand
your diagnosis.  In particular, your age, your PSA level, the Gleason
score, and whether or not your doctor felt anything unusual in digital
rectal examination are all important.

Patrick Walsh's book Guide to Surviving Prostate Cancer is a good source
of information.  Don't reject any form of treatment, including surgery,
until you understand all the advantages and disadvantages of all of them.

> Will some of you be good enough to let me hear from you via email about
> this method?  I understand it only kills the cancer cells.
>
> Thank you for your help in this matter.
>
> Edward
Robert Austin - 01 Nov 2004 03:35 GMT
>I have been diagnosed with very little prostate cancer.  Out of 14
>snippets taken during my biopsy, only one showed a trace of just 5%.
>
>I refuse to have the prostatectomy!  However, I have heard wonderful
>things about the freezing procedure.

Hello Edward and all:

Due to my age my doctor leaned toward cryosurgery.  So far I am very
pleased with the results.  As with all other methods of treating PCa
only time will tell whether or not it was completely successful.

I don't know what all the good things you have heard about the
procedure, I came home the next day and it took a few weeks to
recuperate.  I've been through worse things but it was not a walk in
the park.

As for killing just the cancer cells, in the words of my doctor, "They
turn that sucker into a ball of ice, thaw it, and turn it into a ball
of ice again.  That kills everything except the urethra which is not
frozen because of a warm probe kept inserted in it.

Nerves, tissue, everything is destroyed if the procedure is done
properly, if not it the Pc may reoccur.

Sex is still wonderful, but is possible only with the aid of a pump.

Regardless of what option you choose, make sure the surgeon is an
expert in the procedure. You are welcome to write me privately.

Bob Austin

Age 75
PSA 7 Free PSA 12
1st round of biopsies clear, 2nd. 2 positives
Gleason 9
Cryosurgery 03/11/03
Post Op PSA's 0.4
6  Months 0.1
9  Months 0.2
15 Months 0.21

robertbob.austin@NoSpamearthlink.net
jk - 02 Nov 2004 00:08 GMT
> I have been diagnosed with very little prostate cancer.  Out of 14
> snippets taken during my biopsy, only one showed a trace of just 5%.
[quoted text clipped - 8 lines]
>
> Edward

 Kind of like being a "little" pregnant Ed.... whatever you do short of
nothing, will kill the and/or get rid of your prostate. Thus..... no more
ejaculating, possibly incontinence, and erectile dysfunction. Pick your
poison, and choose to life!
Signature


JK Sinrod
Sinrod Stained Glass Studios
www.sinrodstudios.com
Coney Island Memories
www.sinrodstudios.com/coneymemories

Ed Friedman - 02 Nov 2004 21:20 GMT
>   Kind of like being a "little" pregnant Ed.... whatever you do short of
> nothing, will kill the and/or get rid of your prostate. Thus..... no more
> ejaculating, possibly incontinence, and erectile dysfunction. Pick your
> poison, and choose to life!

Actually, intermittent triple androgen hormonal blockade is also an
option.  There are no 15 year statistics available yet, but for patients
with stage T1-3, with an average PSA of 12.7 and an average Gleason
score of 6.6, the results after 8+ years is no prostate cancer (or
treatment related) deaths yet reported for the 109 patients involved in
that study. 0% for 8 years is a far better death rate than that reported
for any surgery or radiation studies, even though those are usually
performed on patients with much lower PSA's.

Ed Friedman
jk - 03 Nov 2004 00:00 GMT
> >   Kind of like being a "little" pregnant Ed.... whatever you do short of
> > nothing, will kill the and/or get rid of your prostate. Thus..... no more
[quoted text clipped - 11 lines]
>
> Ed Friedman

 Sorry I assumed you were leanming toward getting rid of it forever, as
opposed to starving it, with your fingers crossed, and no sex drive. Unless
your Gleason is high, almost anything you do, or don't do, will probably
leave you alive and kicking in 10 years anyway.

Signature

JK Sinrod
Sinrod Stained Glass Studios
www.sinrodstudios.com
Coney Island Memories
www.sinrodstudios.com/coneymemories

Alan Meyer - 04 Nov 2004 06:02 GMT
> >   Kind of like being a "little" pregnant Ed.... whatever you do short of
> > nothing, will kill the and/or get rid of your prostate. Thus..... no more
[quoted text clipped - 11 lines]
>
> Ed Friedman

Ed,

I hadn't seen that.  Have you got a citation for it?

It's surprising to me and makes me wonder if HT is being
properly applied to most patients.  Most of the people who
have died after RP or RT have also had HT, but it didn't
save them for 8 years as this study claims to have done.

Perhaps the usual methods of giving hormone therapy
are less effective than the "intermittent triple androgen
hormonal blockade" that you cite here.  If that's true, it's
a very important fact that people who have failed RP or
RT should know.

Thanks.

   Alan
Stephen Jordan - 04 Nov 2004 06:44 GMT
Quoting Ed Friedman:

>>Actually, intermittent triple androgen hormonal blockade is also an
>>option.  There are no 15 year statistics available yet, but for patients
[quoted text clipped - 4 lines]
>>for any surgery or radiation studies, even though those are usually
>>performed on patients with much lower PSA's.

Alan responded:

> I hadn't seen that.  Have you got a citation for it?

I'd like to see it, too. That regimen, or something very much
like it, might be efficacious in my case.

> It's surprising to me and makes me wonder if HT is being
> properly applied to most patients.  Most of the people who
[quoted text clipped - 6 lines]
> a very important fact that people who have failed RP or
> RT should know.

The drugs used for triple blockade (ADT3) are a LHRH agonist such
as Zoladex®, an anti-androgen such as Casodex®, and finasteride
(Proscar®). Strum reports good results, especially from the
intermittent course of treatment (NB: Proscar® is continued
during the "off" period).

The results had better be good; that's a very expensive menu.

Strum has written, "ADT is a management issue that continues to
be hotly debated (@ 2002 -- SJ),
and little agreement on the optimal form of ADT has been
reached." He recommends a thorough discussion
with one's physician, as well as careful research by the patient,
before embarking on a course of ADT treatment. Which I intend to
do, although I'm presently on ADT1, a LHRH agonist, solely.

BTW, ADT2 is a LHRH agonist + an anti-androgen.

Regards,

Steve J
__
"Never give in--never, never, never, never, in nothing great or
small, large or petty, never give in except to convictions of
honour and good sense. Never yield to force; never yield to the
apparently overwhelming might of the enemy.''
--Sir Winston Leonard Spencer Churchill
Leonard Evens - 04 Nov 2004 15:42 GMT
>>>  Kind of like being a "little" pregnant Ed.... whatever you do short of
>>>nothing, will kill the and/or get rid of your prostate. Thus..... no more
[quoted text clipped - 30 lines]
>
>     Alan

Keep in mind that there is a vast difference between treating (a)
patients who have just been diagnosed through PSA testing followed by
biopsy and (b) those who have had a primary treatment such as surgery
and radiation and subsequently had a PSA recurrence.

First, for patients in category (a), the disease is at a much earlier
stage, probably at least 5 years earlier.  Most of these patients would
be doing fairly well for five years even without treatment.  Second,
patients are put on HT after PSA recurrence because it is believed that
their cancers have metastasized.  That selects out an even higher risk
population from all those treated by surgery or radiation.

It should also be noted that even for patients with PSA recurrence,
there is some difference of opinion about when to begin HT.  Many
experts think it should be started immediately, but Walsh seems to think
that it should be delayed until clinical symptoms of metastatic cancer
develop.  I believe that there may be some recent evidence that starting
it earlier may prolong life, but it is by no means settled yet.

So this is really a comparison between apples and oranges.

Use of HT as a primary treatment for early prostate cancer is not
generally recommended by the great majority or urologists or others
treating prostate cancer.   If I understand Strum, for example,  even he
seems to be recommending it for cases where there is a good chance the
cancer has already spread because of relatively high PSA and high
Gleason score.   Such therapy might be appropriate in specific cases,
but a typical patient with moderate PSA and Gleason in the range 5-7
probably should still consider either radiation or surgery.   But note
that often a short term use of HT is recommended in combination with
radiation because it seems to make the cancer cells more susceptible to
radiation damage.  I believe they are now trying to determine the
optimum amount of HT to use in such circumstances.
Ed Friedman - 04 Nov 2004 20:33 GMT
> Keep in mind that there is a vast difference between treating (a)
> patients who have just been diagnosed through PSA testing followed by
[quoted text clipped - 7 lines]
> their cancers have metastasized.  That selects out an even higher risk
> population from all those treated by surgery or radiation.

Leonard,

What you say about the disease being at an earlier stage for patients
recently diagnosed (a) vs. those having failed local therapy (b) is
true.  However, can you produce any reference for a study of patients
(a) whose starting PSA is around 12.7 in which no prostate cancer
related deaths are seen after 8 years other than the Leibowitz and
Tucker study?

Ed
Leonard Evens - 04 Nov 2004 21:40 GMT
>> Keep in mind that there is a vast difference between treating (a)
>> patients who have just been diagnosed through PSA testing followed by
[quoted text clipped - 17 lines]
> related deaths are seen after 8 years other than the Leibowitz and
> Tucker study?

I haven't searched the literature on that speicific question, so the
answer is that I can't.  But I don't see the significance of that.
Patients with prostate cancer who start off with a PSA greater than 10
are at increased risk of metastatic cancer in any case.  You would
expect a significant number of such patients who are treated with RP or
radiation to suffer treatment failure.  If they don't receive followup
HT, some of them will die.   Presumably the argument for the Liebowitz
approach is that for such men, an appropriate kind of hormone therapy
started very early is superior to waiting for symptoms to appear.  From
my reading, I believe there is controversy about that.

It is important not to focus in on one particular study.  In time these
matters will be settled.

If you constructed your model purely as an intellectual challenge, then
you should certainly pursue the matter and submit your paper for
publication.  You may make an important contribution.   But if part of
the motivation is to deal with your own actual or potential prostate
cancer,  I think you may get into trouble.  You know the saying that a
doctor should not treat himself.  The same applies when doing research.
 If you are personally involved in this way,  it is very hard to be
objective.  You should avoid making decisions on your own medical care
based on what you think you have uncovered as a researcher.

> Ed
Ed Friedman - 05 Nov 2004 19:24 GMT
> If you constructed your model purely as an intellectual challenge, then
> you should certainly pursue the matter and submit your paper for
[quoted text clipped - 5 lines]
> objective.  You should avoid making decisions on your own medical care
> based on what you think you have uncovered as a researcher.

Leonard,

Thank you for your concern.  I have already made the decision that if I
have a growing prostate cancer, no matter what the stage or gleason
score, I will be going to Dr. Leibowitz and Dr. Tucker for treatment.  I
consider that the chance of their patients developing growing prostate
cancer (PCa) in the future is small, but remote.  I believe that I can
improve on their treatment slightly to bring that chance to close to
being impossible.  Also, I predict that their followup optional
treatment of high dose testosterone replacement therapy will result in
enormous increases in the life expectancy of those patients who avail
themselves of it.  I only wish there were some way to get their final
treatment without first having to get PCa.

As a mathematician you can appreciate that sometimes a model takes on a
life of its own.  This is the case with what I am doing.  PCa is full of
intriguing studies that seem full of contradictions, e.g., biphasic
response of LNCAP to T and DHT, studies showing that T promotes PCa,
studies showing that T kills PCa.  As I study the literature I am
learning new things almost daily.  The best part is when the model is
complete enough to start making predicitions.  Then finding that
experiments have already been done that verify what you had just
predicted is a great thrill.  At this point I am writing my first draft.
Every experiment on early stage PCa that I can find is consistent with
my model (the last little piece fell into place last night).

Ed
Ed Friedman - 04 Nov 2004 20:27 GMT
> Ed,
>
[quoted text clipped - 14 lines]
>
>     Alan

Alan,

Before answering your questions, let me give you a little information
about my background.  I received a Ph.D. in Biophysics and Theoretical
Biology from the University of Chicago in 1993, but since then have been
working as a computer specialist and just doing theoretical modeling in
my spare time.  I became interested in prostate cancer when I had a
spike in my PSA in May of 2004.  I have become so fascinated by this
topic that I am currently preparing a paper for submission detailing an
entire theoretical model for early stage prostate cancer.  I have shown
my model to three major faculty members at the University of Chicago -
the current chairman of Health Studies, the former chairman of
Theoretical Biology, and a doctor in Geriatrics who is currently doing
research in prostate cancer.  None of them could fine any flaws in my
model, and all of them urged me to publish it as soon as possible.

As part of my research, I have come across fascinating articles which
are not part of the general knowledge of the public (or most doctors),
but which are predicted by my model.

To answer your specific questions, there are two reasons that HT does
not work for 8 years when used by most doctors.  First, what kills the
patient is the growth of androgen independent prostate cancer(PCa)
cells.  The more total PCa cells you have, the more likely you are to
have mutations that are androgen independent. In the study I was talking
about, hormone therapy was started early in order to minimize the total
number of PCa cells and thus minimize the chance of any of them being
androgen independent.  The reference to this paper is
http://theoncologist.alphamedpress.org/cgi/content/full/6/2/177
I have been in contact with the authors, and since that paper was
published, 1 of the 110 patients was found to have ductile
adenocarcinoma and has since died of his cancer.  Of the 109 other
patients with primary prostate adenocarcinoma, there have been no PCa
related deaths, and none currently in danger of dying from it.

Also, they have saved lives of patients who have failed RP or RT, by
using a similar initial treatment coupled with antiangiogenic drugs.  If
you want to take the time to sift through 256 slides, you can see for
yourself some such patient records by going to:
http://www.prostateweb.com/ppt/Fullerton_March_23_2004.ppt

Also, I have been unable to loate any article that has shown that T
promotes prostate cancer growth, except when it is converted to DHT.
This means that doctors are aiming at the wrong target when they try to
minimize T.  The only reason that it is effective at all is because it
lowers the level of DHT.  The most recent reference that illustrates
this is the article at:
http://147.52.72.117/OR/2004/volume11/number6/1325.pdf

Ed Friedman
Alan Meyer - 05 Nov 2004 01:16 GMT
> > Ed,
> >
[quoted text clipped - 65 lines]
>
> Ed Friedman

Ed,

Thanks for this extensive response, and thank you for doing this
research.

I agree with Leonard that, in spite of the results these doctors
are getting, surgery or radiation still seems like a better first line
treatment than HT for all but quite old patients.  Having had both
radiation and HT, I can say that the radiation effects bothered
me less than the HT effects and taking hormones for 8, 10 or
more years is not something I'd want to do unless I had to.
Furthermore, I couldn't help but want to try a curative
treatment first, before I chose one that could only delay
the growth of the cancer.

However, the PCa community is in desparate need of options for
what to do if RP or RT fails.  The results these doctors are
getting do seem a lot better than the standard results.  If they
pan out and can be duplicated by others, they are good candidates
for setting a new standard.

Personally, if I failed treatment (hasn't happened yet), I'd
seriously consider this triple intermittent ADT.  I don't see
why it would be much worse than the standard Lupron or
Zoladex only treatment.

Leonard said:

> It is important not to focus in on one particular study.  In
> time these matters will be settled.

From an academic point of view, I'm sure he's right.
But if your life is at stake, as it is for people on HT,
there isn't time to wait for all the results to be in and
all the dust to settle.

This therapy is an extension of a very standard therapy.
The doctors aren't recommending something totally
new using mechanisms that are totally new and un-
understood.  They are taking something that is known
to work to some degree, administering the identical
therapy, and adding more to it.  From where I
stand, I'm inclined to think that the risk of wait-
and-see may be greater than the risk of jumping
in.

But as I so often must say, I'm no expert.

   Alan
Alan Meyer - 02 Nov 2004 06:13 GMT
> I have been diagnosed with very little prostate cancer.  Out of 14
> snippets taken during my biopsy, only one showed a trace of just 5%.
[quoted text clipped - 8 lines]
>
> Edward

Edward,

As others suggested, find out what your PSA, Gleason, and staging
are.  The biopsy result is relatively good (if having cancer can be
considered good), but other factors are also important in figuring
out how aggressive and advanced the cancer is.  Under any
circumstances you'll want to spend some time investigating your
options, but if all the signs are good, you have still more time.

Your age is also significant.  PCa tends to be more aggressive
if you get it when you're relatively young.

The two traditional therapies are radiation and surgery.
Cryotherapy is a relative newcomer.

I shared your fear of surgery and opted for radiation instead.  So
far, I've been satisfied with my choice and with the mildness of the
after effects.  Radiation is painless and I was able to go to work
every day that I received it - only taking two days off for each of two
HDR brachytherapy procedures I got.

Research radiation and cryotherapy.  Research prostatectomy
too.  If I were you I wouldn't be too quick to rule anything out, or
too quick to select one therapy over others.

Another good idea is to meet the people who would perform
the procedures.  You may find that one of them (the urological
surgeon, the cryosurgeon, or the radiation oncologist) inspires
more confidence in you than any of the others.  That too is a
factor in the choice.

Best of luck.

   Alan
Steve Kramer - 02 Nov 2004 18:44 GMT
Edward,

Having provided merely your biopsy results, I'm guesing that you haven't put
a lot of effort into research.  As this is a life and death matter, I
suggest you do so immediately.

Without your age, Gleason score, PSA, or Stage, there is no way we can even
hazard a guess as to what your options are or are not.  I can tell you that
if you have a Gleason of 5 or 6, low PSA, and a Stage of T1a (which is quite
possible with one needle of 14 showing 5%) and are in your 50s or 60s, some
here was consider you a damned full for not considering radical
prostatectomy.

But, to answer your question, cyro will freeze your prostate killing it and
everying in it including your cancer, or that is the hope.  There are a few
here that have tried it.  It seems to have worked for one, maybe not worked
for a couple and the others are somewhere in Limbo.

Signature

Prostate Cancer Survivor (so far), not a doctor
PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3bN0M0
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron (1 mo) 07/21/2003 @ 48
PSA  .07 .05 .06
Lupron (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50)
non illegitimi carborundum

> I have been diagnosed with very little prostate cancer.  Out of 14
> snippets taken during my biopsy, only one showed a trace of just 5%.
[quoted text clipped - 8 lines]
>
> Edward
Steve Kramer - 02 Nov 2004 18:49 GMT
that was supposed to be "some here would consider you a damned fool".  Fat
fingers.

Signature

Prostate Cancer Survivor (so far), not a doctor
PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3bN0M0
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron (1 mo) 07/21/2003 @ 48
PSA  .07 .05 .06
Lupron (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50)
non illegitimi carborundum

> Edward,
>
[quoted text clipped - 26 lines]
> >
> > Edward
Alan Meyer - 04 Nov 2004 06:12 GMT
> ... some
> here was consider you a damned fool for not considering radical
> prostatectomy.
...

I agree it would be a mistake not to consider radical prostatectomy.
It is a proven life saver.

But I don't think it would be foolish to conclude, as some do,
that it's a mistake for a younger man to choose any other treatment.

I admit that my own experience is still too recent to draw
any conclusion from.  But so far at least, I'm not sorry I chose
radiation at age 57.

Just like prostatectomy, radiation is a proven cancer killer.
Like RP, it doesn't always work.  Like RP, it can be applied
skillfully or clumsily.  But when it's done well, I believe it does
work.

Unfortunately, in some of us cancer has already established
itself outside the area where either RP or RT can reach it.  For
those men, treatment fails no matter which modality they
choose.

Even more unfortunately perhaps, some of us are treated
by surgeons or radiologists who don't do a good job and
leave some cancer behind.

So picking a good doctor is just as important as picking
a good treatment modality.

   Alan
Steve Kramer - 04 Nov 2004 17:57 GMT
Just so there is no misimpression, including for the new lurkers, I am not
stating that Radical Prostatectomy is the only solution.  I'm just saying
that is should not be dismissed out of hand.

Signature

Prostate Cancer Survivor (so far), not a doctor
PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3bN0M0
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron (1 mo) 07/21/2003 @ 48
PSA  .07 .05 .06
Lupron (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50)
non illegitimi carborundum

> > ... some
> > here was consider you a damned fool for not considering radical
[quoted text clipped - 29 lines]
>
>     Alan
Alan Meyer - 05 Nov 2004 01:01 GMT
> Just so there is no misimpression, including for the new lurkers, I am not
> stating that Radical Prostatectomy is the only solution.  I'm just saying
> that is should not be dismissed out of hand.

I agree with that 100%.

  Alan
 
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