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Medical Forum / Diseases and Disorders / Prostate Cancer / September 2006

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What about Dr. Myers opinion?

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JohnHace - 08 Sep 2006 00:33 GMT
As I am trying to choose between RT and RP, I realized that I have
heard of several MD's with PC that chose RT. I'm not saying that no MD
has ever chosen RP, I've just not read anything about it.

The one I remembered that really struck me was Dr. Charles "Snuffy"
Myers. For those who don't know, he is a medical oncologist who has
been involved with PC for years. I went back to his web site and read
his story. It is remarkably similar to mine. He was diagnosed in 1999
at 55, I was 57 when diagnosed. His PSA was 20.4, mine started at 20.3
and dropped to 13.8. His Gleason was 3+4, same as mine. He had a
palpable lump on his gland where I have none. So, his situation was a
little worse than mine, but not much.

You can read his story "The Physician Becomes the Patient" at
http://www.prostateforum.com/sample.htm. In it he said he chose RT
because the Partin tables show "80-90% chance that the cancer had
penetrated the prostate capsule and spread to the fatty tissue
surrounding the prostate gland. There was a 9-14% chance that the
cancer had spread to the lymph nodes that drain the prostate gland."

He went on to say "I would have been pleased if radical prostatectomy
had been a reasonable option. Unfortunately, if you study the Partin
tables or other publications on radical prostatectomy, surgery does not
do a very good job of curing men with cancers like mine. "

That's pretty powerful. This was written in 1999. So, I purchased
several back issues of his newsletters where he updated his progress.
In Volume 7, Number 7 in 2003 he said:

"For men with a Gleason 6 or lower and a PSA under 10 ng/ml, the
results reported for temporary seed implants plus 3-D conformal or IMRT
radiation are equal to or better than the best results reported for
radical prostatectomy.

For men with more aggressive cancers associated with a poor
Gleason-related prognosis, a PSA over 10 ng/ml, a more extensive cancer
in the prostate gland, or the presence of capsular penetration, 3-D
conformal or IMRT combined with radioactive seed implantation currently
offers results that are clearly superior to the best surgical
approaches."

Can anyone refute this logic?

Thanks,

John
Alan Meyer - 08 Sep 2006 01:17 GMT
...
> That's pretty powerful. This was written in 1999. So, I purchased
> several back issues of his newsletters where he updated his progress.
[quoted text clipped - 13 lines]
>
> Can anyone refute this logic?

Here's two cents worth of opinion (or maybe that price is a bit
high) from a guy who can't really claim to know what he's
talking about, but isn't 100% sure that the experts can make
any stronger claims to certainty about their opinions.

After arguing against a number of folks who said that surgery was
better than radiation, I'm now going to go the other way and argue
against the view that radiation is better than surgery.

The logic that says that radiation is more effective against extra-
prostatic extensions seems reasonable to me, and is supported
by some prominent surgeons (Drs. Partin and Scardino for example).
However I'm not sure that the data is comprehensive or conclusive
enough to point to a clear decision one way or the other.

The problem, as far as I can see, is that there are a myriad of
studies with conclusions that contradict each other.  My sense
is that the best studies - the ones with the largest sample sizes,
most valid study designs, and most reasonable selection of
patients to include - show fairly comparable outcomes for
well done surgery vs. well done (no pun intended) radiation.

My personal decision was to go with radiation because I thought
it offered good chances for success and fewer side effects.  I
too also thought that my Gleason 4+3 might be better treated
with it.  But I'd be kidding myself if I said my decision was
based on highly objective factors.  To tell the truth, knives
scare me a little more than xrays - though I've found that some
men here with extensive experience with xrays (I'm thinking of
Curtis Palmer, who taught courses on the subject) felt exactly
the opposite.  And I liked the rad oncs I met more than the
surgeon I met.

You seem to be leaning towards radiation.  I personally think
that's a good choice if you can be treated at an advanced,
experienced center - which you seem to be able to do.  But
you may want to give up the belief that your choice can be
clearly justified by science as better than the alternatives.

   Alan
Beverley - 08 Sep 2006 03:03 GMT
The only thing I can say is my husband's PSA was 5.1 and then 4.8. His
Gleason was a 6 (3+3) and his fPSA was 8%. We banked his life on
brachytherapy with Iodine 125 seeds after 5 weeks of EBRT on IMRT.

For men with higher PSA and Gleason scores it seems that they do recommend
RT but for some reason our rad-onc (Massey Cancer Center) doesn't do
brachytherapy on scores higher than a Gleason 6 and a PSA over 10. Yet I've
read that they are seeing very successful outcomes with many men with high
Gleasons and PSA's using this combined RT. I think I'm referring to RCOG's
stats on the subject.  I'll assume there is some controversy about these
higher risk men.
Bev

> As I am trying to choose between RT and RP, I realized that I have
> heard of several MD's with PC that chose RT. I'm not saying that no MD
[quoted text clipped - 42 lines]
>
> John
Dick Smith - 08 Sep 2006 07:03 GMT
> The only thing I can say is my husband's PSA was 5.1 and then 4.8. His
> Gleason was a 6 (3+3) and his fPSA was 8%. We banked his life on
[quoted text clipped - 8 lines]
> higher risk men.
> Bev

My dad had aggressive PCa and his urologist suspected it had penetrated
the capsule therefore his urologist suggested a combination of
radiation and seeds.

Unfortuantely, the combination didn't work, or it was too late and the
cancer had already spread.
ron - 08 Sep 2006 03:15 GMT
Hi John...I have a lot of respect for Dr. Myers, he has helped
countless men.  His background in cancer research and then his own
personal dealings with PCa only add to his ability to make keen
observations and correct decisions.  That said, I'd sure like to know
what articles or data he is basing the following comment upon.  I don't
disagree with what he says, I'd just like to know where it comes from.

> For men with more aggressive cancers associated with a poor
> Gleason-related prognosis, a PSA over 10 ng/ml, a more extensive cancer
> in the prostate gland, or the presence of capsular penetration, 3-D
> conformal or IMRT combined with radioactive seed implantation currently
> offers results that are clearly superior to the best surgical
> approaches."

RCOG and Hopkins are, IMO, centers of excellence for [seeds + RT] and
RP respectively.  Both centers have published their long-term results
stratified by risk group.

RCOG SI+EBRT study (F. Critz, W. Williams, A. Levinson, J. Benton, F.
Schnell, C.  Holladay, and P. Shrake; Poster Abstract 692 at the 2003
AUA meeting; NOTE, this is a poster, NOT a peer-reviewed publication)

Hopkins study (M. Han, A. W. Partin, M. Zahurak, S. Piantadosi, J.
Epstein and P. C. Walsh; J. Urol., 169, 517-523, 2003; the paper can be
found at
http://www.prostate-help.org/download/jhnomo.pdf)

The nice thing about these two techniques is that they both used a
common definition of failure (PSA>0.2 ng/ml is a failre; note: RCOG has
recently made a slight change to their method of calling a failure) so
direct apples to apples comparisons are possible without having to make
too many assumptions.  When I compared the data, I found their success
rates were too close to call for low risk men, but as you moved to
higher risk men, RP started showing an advantage.  This surprised me as
I thought RT would show  an advantage in these cases since it
irradiates somewhat beyond the capsule.  Further reading on the subject
suggested that high-grade PCa may show signs of being  radiation
resistant for two reasons.  First, dense tumors lack oxygen in their
interior.  Radiation does not interact with and destroy PCa cells
directly, rather the radiation ionizes oxygen which then interacts with
the cancerous cell in a process whereby the cell winds up damaged.
Second, advanced PCa cells often contain mutated forms of proteins that
are required to kill the now damaged cancerous cells.  The mutated
forms of these proteins are not as effective in bringing about
apoptosis as the non-mutated versions.

A number of studies have begun to appear that examine the efficacy of
surgery and radiation with advanced PCa, Zincke's paper is a good one
(BJU Int. 2005 Apr;95(6):751-6; Radical prostatectomy for clinically
advanced (cT3) prostate cancer since the advent of prostate-specific
antigen testing: 15-year outcome; Ward JF, Slezak JM, Blute ML,
Bergstralh EJ, Zincke H.).  A synopsis or review of this paper can be
found at

http://www.mayoclinic.org/news2005-rst/2745.html

My honest opinion is that at this point in time there is no clear,
undeniable signal that suggests one modality (RP or SI+RT) is better
than the other.  It's a plain, old-fashion crap shoot and not only does
it depend upon the doctor's skill, but it also depends on things like
your DNA.  If you're psychologically more comfortable with SI+EBRT go
for it, if you feel the better doc is the surgeon, go with him.  You
will make the right choice for you...Best wishes and good health, ron
JohnHace - 08 Sep 2006 16:07 GMT
Ron,

I appreciate your posts. They're always insightful.

But there is one point I'd like to learn more about. When you say:

> Further reading on the subject
> suggested that high-grade PCa may show signs of being  radiation
[quoted text clipped - 6 lines]
> forms of these proteins are not as effective in bringing about
> apoptosis as the non-mutated versions.

What you say makes perfect sense if we're talking about only XBRT,
especially if it were the older 3D conformal beam. There were a lot of
failures with that because it was difficult to get the dose over 70 Gy.
Now with IMRT, doses over 80 Gy are more common. But, I'm considering
SI+IMRT. With the combination, doses inside the gland can be over 200
Gy. I think most any living tissue will succumb to a dose of that
level.

> A number of studies have begun to appear that examine the efficacy of
> surgery and radiation with advanced PCa, Zincke's paper is a good one

I looked at this paper, but, again, they don't deliniate the type of RT
used for comparison. One thing we know, in a study of 15 year survival,
we're looking at technology used 15 years ago. If I had to choose
between surgery and 15 year old radiation technology, I'd go for the
surgery. But RT today is a completely different ballgame.

I think a form of wide excision surgery could cure me now, but I
believe it could take both nerve bundles and I'm not sure I want to
live that way. I think that SI+IMRT can treat as large, or larger, area
and leave the nerves intact.

As you say

> It's a plain, old-fashion crap shoot

in the game of "You Bet Your Life".

Thanks,

John
Bob Anthony - 08 Sep 2006 05:12 GMT
Again, I will repost my earlier response:

Quotations from Dr Meyers website:
> Dr. Myers believes that the available evidence indicates that many
men > diagnosed today have cancers that are not going to be cured by
surgery > or radiation therapy. All too often, men undergo these
procedures only > to experience a relapse after a period ranging from
several months to > several years.

And

> The patients most likely to be cured of prostate cancer by radiation
> therapy or surgery have Gleason scores of 6 or lower and a PSA of 10
> or less.

And

> I ruled out watchful waiting for a number of reasons. My life
> expectancy is longer than ten years. I have no other significant
[quoted text clipped - 4 lines]
> radiation therapy. If I let the cancer progress at all, this option
> would disappear.

I don't know, maybe I'm dense or whatever. Is he not contradicting
himself? If Dr. Myers believes that if most men are incurable that are
diagnosed today, then why bother at all?

Should pts with GS scores greater than >6 just go on HT without first
trying either RP or RT since he indicates that they are incurable in the
first place? (I do understand the Partin Tables here in his case).

Dr. Myers has a GS of 7, clinically I may add, and it could be even
higher at pathology. But since he chose RT, he will not know for sure to
which he does admit to. But if he had "let the cancer progress", then he
goes on to state, "what can be successfully treated with surgery or
radiation therapy" may be lost.

I'm having a tough time deciphering to just what he is saying. I'm under
the assumption that Pca that is found today in most of men are indeed
curable due to earlier detection and better treatments.

B.A.
JohnHace - 08 Sep 2006 14:02 GMT
Bob,

I don't see a contradiction.

>  > Dr. Myers believes that the available evidence indicates that many
> men > diagnosed today have cancers that are not going to be cured by
> surgery > or radiation therapy.

He didn't say "most" men, he just said "many" men. So, I don't think
he's saying treatment should not be undertaken.

>  > The patients most likely to be cured of prostate cancer by radiation
>  > therapy or surgery have Gleason scores of 6 or lower and a PSA of 10
>  > or less.

Again, he's saying "most likely". I don't think he's saying men in a
higher risk group can't be cured, just that men in a lower risk group
have a better probability of cure.

I'm going to have a treatment. I'm just trying to figure if it's going
to be RT or RP.

Thanks for responding.

John
Bob Anthony - 08 Sep 2006 15:00 GMT
Hi John:

I told you that I was dense ;)
I just get a bit befuddled, perhaps unnecessarily, when he says "many"
men diagnosed today are not going to be cured by surgery or radiation
and those "most" likely to be cured have a GS of 6 or less and psa's of
< 10 because the message sounds muddled and so much more pessimistic.
Looking at other doctor's opinions and nomograms by comparison, I found
what he was saying to be somewhat of a contradiction as well as
depressing. Just my take on it. If you look at the SK nomogram for
instance, you find only a 3% difference at the 7 year outcomes for
recurrence between GS 6 and GS 7 cancers. I believe with the newer and
more precise treatments that are available today, that number may even
be better, hopefully.
Good luck on your treatment of choice and wishing you all the best for a
great outcome!

B.A.
ron - 08 Sep 2006 15:26 GMT
Bob Anthony wrote...snip...
"many" men diagnosed today are not going to be cured by surgery or
radiation and those "most" likely to be cured have a GS of 6 or less
and psa's of < 10

Bob...Kinda sounds like what Dr. Willet Whitmore, the father of
urologic oncology, said some time ago, "For a patient with prostate
cancer, if treatment for cure is necessary, is it possible? If
possible, is it necessary?"...Best wishes and good health, ron
Bill - 08 Sep 2006 15:52 GMT
Dr. Myers' thinking makes perfect sense to me.
* RP only eliminates all of the disease if all of the disease is
located within the gland and other tissues removed.
* If there is a likelihood that that all of the disease is NOT located
within the gland or other tissues removed [but not systemic] then it
stands to reason that RT to the gland, seminal vesicles, local nodes,
and prostate bed offers a better chance of cure than RP. It may be the
equivalent of RP + SRT in one course of Tx.

Bill Denton
RP 2/12/02
PSA .06
Memphis
Leonard Evens - 09 Sep 2006 02:23 GMT
> Dr. Myers' thinking makes perfect sense to me.
> * RP only eliminates all of the disease if all of the disease is
[quoted text clipped - 4 lines]
> and prostate bed offers a better chance of cure than RP. It may be the
> equivalent of RP + SRT in one course of Tx.

I think this reasoning is generally accepted by those who treat prostate
cancer.  But the crucial point is that you should have some strong
reason for believing the cancer, while still local, has extended beyond
what surgery might reach.

> Bill Denton
> RP 2/12/02
> PSA .06
> Memphis
JohnHace - 09 Sep 2006 17:21 GMT
> I think this reasoning is generally accepted by those who treat prostate
> cancer.  But the crucial point is that you should have some strong
> reason for believing the cancer, while still local, has extended beyond
> what surgery might reach.

Leonard,

I guess that is a good reason, if not THE reason for the Partin tables.

Dr. Partin gives me 63% probability of extra-capsular penetration.

On the other hand, even if I don't have extra-capsular penetration, the
SI+IMRT looks like a good option. The radiation doses now are high
enough to anihilate the prostate, the internal sphincter remains
intact, the nerves are spared, and the primary cause of any ED is
usually due to blood vessel damage. It turns out that this type of ED
responds well to Viagra. If I come away from this with nothing more
than a Viagra habit, I'm a happy guy.

John
Leonard Evens - 10 Sep 2006 14:52 GMT
>>I think this reasoning is generally accepted by those who treat prostate
>>cancer.  But the crucial point is that you should have some strong
[quoted text clipped - 16 lines]
>
> John

If I understand correctly, your diagnosis is T1c, Gleason 7=3+4 and PSA
greater than 10.   The probability that your cancer is not in the
seminal vesicles or lymph nodes would appear to be about 80 percent.
While that doesn't guarantee the cancer hasn't spread, it is the only
evidence you have available on which to base a decision.   So the
question is the utility of surgery or radiation in killing the cancer in
the case it has penetrated the capusule but is still local, which seems
about as likely as its still being contained in the prostate.  I buy the
argument for radiation, but it is not clear to me from what I've read
that adding seeds to the mix would help.   3D conformal radiation with
IMRT seems capable of delivering very high doses with minimal damage to
surrounding tissues.   Scardino, in particular recommends against
combination approaches instead of straight external beam therapy of the
above kind.   You should at least read what he has to say and compare it
 to your other sources of information.

Of course, what may trump everything else is what type of high quality
treatment is available to you.  If the best practitioners you have
access to use the combination therapy,  you should go with it.
ron - 10 Sep 2006 16:11 GMT
Leonard Evens wrote...snip...
> Scardino, in particular recommends against
> combination approaches instead of straight external beam therapy of the
> above kind.

Leonard...Does Scardino give a reference or rationale for his
position?..ron
Leonard Evens - 10 Sep 2006 17:09 GMT
> Leonard Evens wrote...snip...
>
[quoted text clipped - 4 lines]
> Leonard...Does Scardino give a reference or rationale for his
> position?..ron

The discussion is on pp 324-325 of his book.  He gives a reference only
to a paper reporting efficacy of such therapy, but he doesn't give any
references to studies which directly compare the two methods head to
head in a single study.   But if you read the entire chapter, you see
that he goes into great detail about the various modes of radiation
therapy, including work done at Sloan Kettering with brachytherapy, and
that there are many references to specific issues.  It was my impression
that he didn't find the cure rates claimed for combined approaches
adequate to cure a higher risk cancer any better than 3D conformal with
IMRT.   Hence, he thought there was no point in taking on what he sees
as additional risks from the combined approach.

But go read it for yourself.  I got the paperback edition of his book at
Borders for $16.  It is well worth the price for anyone interested in
prostate cancer.
JohnHace - 10 Sep 2006 18:01 GMT
First let me say that I really appreciate everyone's input on this
particular thread. I started this thread because I'm trying to decide
between RP and RT. As I'm now leaning heavily toward RT, if anyone has
a good reason why someone in my situation would be making a mistake,
I'd rather find out now than later.

I also realized that each time someone made a point, I seem to make a
counterpoint. I'm not trying to act like a know-it-all, it's just that
most of these points I have gone over in my mind many times before in
trying to make sense of this situation.

Never the less, I really appreciate what everyone has to say.

Now for my next counterpoint:

>I buy the
> argument for radiation, but it is not clear to me from what I've read
[quoted text clipped - 4 lines]
> above kind.   You should at least read what he has to say and compare it
> to your other sources of information.

Leonard, I've read most all of the books mention around here and quite
a few others. Of all the books, I think Scardino's is my favorite. He
seems to give a fairly even handed assesment of RT in general. He
points out that "conventional" XBRT was crude and not very precise and
approximately one third suffered side effects like rectal damage. He
goes on to say that 3D-CRT reduced the problem down to 17%. Then he
says that IMRT reduces it to 2 to 3 percent. His diagram on page 303
clearly shows the differences in these procedures. So far, so good.

But, then when he talks about combining external beam with seeds, he's
talking about "conventional" external beam. He calls it a "low-tech,
riskier substitute" and that the error rate and resultant side effects
may be multiplied. Well, I would agree. I would not want to have seeds
with "conventional" external beam radiation. But, he never addressed
SI+IMRT. He devoted 17 pages discussing XBRT, 11 pages regarding seeds,
and only one page to combined therapy. I think he really short-changed
this important subject.

He says, "There is no evidence that cancers are cured more effectively
with combined approaches." Critz at RCoG (over 10,000 patients) and
Dattoli (over 8,000) have published a number of papers to show there is
evidence. I think Scardino dropped the ball on this one.

But, I appreciate your mentioning it.

John
Bob Anthony - 10 Sep 2006 19:26 GMT
> But, he never addressed
> SI+IMRT. He devoted 17 pages discussing XBRT, 11 pages regarding seeds,
> and only one page to combined therapy. I think he really short-changed
> this important subject.

But in the next paragraph Scardino did state "Given the wide
availability of effective, high-dose, modern 3-D conformal radiation and
IMRT, I see little justification for the risks involved in the
combination approach". Although it the message appears to be muddled.
I would assume this does include SI+IMRT.
He also goes on to state that combining hormones and IMRT is not worth
the effort as well because combining hormones with radiation (IMRT) is
comparable to adding 5Gy to the dose. Then, why not just add the 5Gy?
I seem to get the impression that by using combined initial therapies,
Scardino considers them to be riskier overall.
There is a website where you can ask such a question. I'd be curious as
to what they would have to say as well.

www.theprostatebook.com

B.A.
I.P. Freely - 11 Sep 2006 00:55 GMT
Just Google something like combined radiation seeds prostate. There are
many data and opinions and studies out there shedding some light on the
issue.

I.P.

>> But, he never addressed SI+IMRT. He devoted 17 pages discussing XBRT, 11 pages regarding seeds,
>> and only one page to combined therapy. I think he really short-changed
[quoted text clipped - 16 lines]
>
> B.A.
Ron B - 10 Sep 2006 19:34 GMT
I had an RRP in March of '05.

PSA about 7...Gleason 3+4 (which after pathology turned out to be 3+3=6)

Confined to capsule, no SV or lymph node involvement.

Before the surgery, and I was as scared as could be...

Dr. Catalona said...

You have to be prepared to buy the 'whole package'...meaning...the
surgery and possible RT.

He said that because if you were told later that you needed RT AFTER the
surgery...you wouldn't be shocked or disappointed. (Right.  :-)

It didn't make me feel any better...but it's the truth.

I didn't need the RT...so I feel very grateful.

I just tell this tale to help John and maybe help with some of his
thoughts.

I gotta say that I am VERY impressed by the expertise shown by the group
on this topic.

That's why I'm here.

Best of health to all,

Ron B.

Chicago
Leonard Evens - 10 Sep 2006 22:54 GMT
> First let me say that I really appreciate everyone's input on this
> particular thread. I started this thread because I'm trying to decide
[quoted text clipped - 42 lines]
> Dattoli (over 8,000) have published a number of papers to show there is
> evidence. I think Scardino dropped the ball on this one.

Walsh in his 2001 book, specifically discusses the RCOG results as of
that date.  I don't know if they have modified their approach since
then.  He claims that their comparison between results for surgery and
their approach is comparing apples and oranges.  I'm not qualified to
evaluate whether he is right or not.

I've looked at the RCOG website, and I am not clear  about exactly what
they do.  I doubt it it is simply seeds plus 3D conformal radiation with
IMRT.   Presumably their studies are not based on some recent change in
their procedures.   My guess is that Scardino is well aware of what they
do there, but what do I know.

Anyway, in making a choice, since none of us is really qualified to
evaluate competing claims,  we just have to make the best guess we can.
 You seem to have thought it all out, and I am certainly in no position
to question the validity of your choice.

Good luck whatever you finally decide to do.

> But, I appreciate your mentioning it.
>
> John
Leonard Evens - 11 Sep 2006 15:46 GMT
> I've looked at the RCOG website, and I am not clear  about exactly what
> they do.  I doubt it it is simply seeds plus 3D conformal radiation with
> IMRT.   Presumably their studies are not based on some recent change in
> their procedures.   My guess is that Scardino is well aware of what they
> do there, but what do I know.

Let me add that I checked the Sloan Kettering site, and the seeds expert
ther, Zelefsky, who Cardino refers to in his book, is now useing a
combined approach.

> Anyway, in making a choice, since none of us is really qualified to
> evaluate competing claims,  we just have to make the best guess we can.
>  You seem to have thought it all out, and I am certainly in no position
> to question the validity of your choice.
>
> Good luck whatever you finally decide to do.
I.P. Freely - 10 Sep 2006 23:50 GMT
> if anyone has a good reason why someone in my situation would be making a mistake,
> I'd rather find out now than later.

I don't know what your "situation" is, but mine, not even counting my
coexisting unrelated abdominal cancer, ultimately narrowed my options
down to one choice. Factors included PSA level and dynamics, Gleason
grade, age and health, urinary and bowel and sexual performance before
and maybe after tx, lifestyle, potential impacts on that lifestyle, and
extensive examination of my short and long term personal priorities. As
an engineer, controlled radiation didn't scare me. Having had several
surgeries, surgery didn't scare me. Cost was not a factor once I learned
that there are some cutting edge VA facilities out there, two within a
reasonable commute.

But ever so slowly, my research painted out one more portion of the
floor I was standing on. Each little piece of my puzzle -- G8 here,
rapidly rising PSA there, exceptional health there, rejection of one
likely SE or acceptance of another -- slanted me towards one tx or away
from another until one day or week the picture became pretty clear, so I
confidently selected a procedure and a facility and a doctor, and acted.

Two "mistakes"" would be 1) deciding and acting before you've seen and
weighed all the available facts, statistics, professional opinions, and
personal priorities available within a rational search or 2) paralysis
by analysis. Personally, I defined my rational research limit as the
point my literature searches led me "back to my own tracks", i.e.,
nothing new and useful was turning up. If you're at that point and
leaning strongly towards any tx and this group's not calling you an
idiot and backing it up, what the hell . . . do it.

If, OTOH, you have lingering doubts because of incomplete reading or
introspection, you've got time to read or think more. Your cancer has
taken many years -- decades, some oncs believe -- to surface; a few more
weeks or even months won't matter unless your "situation" is unusual.
i.e., a little paralysis is OK if you recognize it and put that time to
good use.

I.P.
Alan Meyer - 18 Sep 2006 15:30 GMT
...
>  I buy the argument for radiation, but it is not clear to me from what I've read that
> adding seeds to the mix would help.   3D conformal radiation with IMRT seems capable of
> delivering very high doses with minimal damage to surrounding tissues.   Scardino, in
> particular recommends against combination approaches instead of straight external beam
> therapy of the above kind.   You should at least read what he has to say and compare it
> to your other sources of information.

It's never been exactly clear to me what the relative risks of brachytherapy
and external beam are.

Brachytherapy adds some surgical risk.  There is anaesthesia,
puncturing of the perineum with the treatment catheters, insertion
of foreign bodies, and some consequent risk of infection - though
the radiation itself probably kills any bacteria that might be around
the seeds.  There is also the possibility of one or more seeds
wandering into other parts of the body.

Are those the risks we are talking about?  From what I've read,
they aren't too risky, though definitely more risky than not having
them.

On the other hand, I have no idea what the relative radiation risks
of EBRT vs Brachytherapy are.  EBRT sends xrays through parts
of the body that are not part of the prostate.  Presumably, seed
implant does much less of that.  With combined therapy, the dose
of EBRT given is significantly lower than with plain EBRT.  So I
don't know (and don't know if anyone knows) whether the pure
radiation risks are lower with combined therapy than with EBRT
alone.

Then there is the dosage issue.  My understanding is that the total
dose delivered by combined therapy is greater than for EBRT
alone.  But I don't know whether that translates into benefit for
the patient.

Another issue to be considered is whether the seed implant will
make the EBRT aiming more effective.  The treatment offered
to John consisted of planting seeds first, then imaging the seeds
each day during EBRT to get exact placement of the prostate.

Again, I don't know and don't know if anyone knows, how much
of an improvement that makes in EBRT aiming.  I wonder if the
primary issues in aiming have more to do with the time and care
taken by the techs than with the specific procedure used.

> Of course, what may trump everything else is what type of high quality treatment is
> available to you.  If the best practitioners you have access to use the combination
> therapy,  you should go with it.

I agree.  If there were a very clear case for monotherapy vs.
combined therapy, one might choose based on that.  But there
doesn't appear to be a very clear case for one or the other.  So
picking the practitioner seems like a reasonable way to go.

   Alan
Bill - 08 Sep 2006 15:54 GMT
Dr. Myers' thinking makes perfect sense to me.
* RP only eliminates all of the disease if all of the disease is
located within the gland and other tissues removed.
* If there is a likelihood that that all of the disease is NOT located
within the gland or other tissues removed [but not systemic] then it
stands to reason that RT to the gland, seminal vesicles, local nodes,
and prostate bed offers a better chance of cure than RP. It may be the
equivalent of RP + SRT in one course of Tx.

Bill Denton
RP 2/12/02
PSA .96
Memphis
ron - 08 Sep 2006 16:06 GMT
> Dr. Myers' thinking makes perfect sense to me.
> * RP only eliminates all of the disease if all of the disease is
[quoted text clipped - 9 lines]
> PSA .96
> Memphis

Bill...I agree that it sounds reasonable that RT should outperform RP
if disease has escaoped the prostate, but remains local.  Are you aware
of any comparative data that supports that view?..Best wishes and good
health, ron
Dick Smith - 08 Sep 2006 16:06 GMT
However if RRP fails, you can get a second chance doing RT to the
prostate area..
Claude - 08 Sep 2006 16:10 GMT
> However if RRP fails, you can get a second chance doing RT to the
> prostate area..

Which was an important factor in my decision to get an RP.
JohnHace - 08 Sep 2006 16:35 GMT
> However if RRP fails, you can get a second chance doing RT to the
> prostate area.

Dick,

I felt the same way and that alone had me initially leaning towards
surgery.

But, then I thought about side effects. Surgery has one set, and RT has
another. If it takes both to cure, you may end up with both.

Also, as I mentioned in another thread, one rad onc showed me a
diagram. The prostate forms a spacer between the bladder and rectum. It
can be hit with high doses of radiation while mostly sparing the other
organs.

Once the prostate is removed by surgery, the bladder drops down to
almost touch the rectum. It is then difficult to radiate the area
without substantial radiation hitting those organs, and more profound
side effects.

Since Partin says I only have a 37% probability of an organ confined
cancer, I really don't like the idea that I would likely need both
treatments.

Thanks,

John
Alan Meyer - 08 Sep 2006 16:46 GMT
> However if RRP fails, you can get a second chance doing RT to the
> prostate area..

One theory about this, expressed to me by a radiation oncologist,
is that if RP fails and salvage RT works, then RT would have
worked originally too without the RP.  If RT fails after RP, then
the RT wouldn't have worked as a primary therapy either.

But, as Ron says, all of this is theory.

In practice, there is a lot dependent on the skill of the practitioner
and the specific characteristics of the patient's disease, and
on dumb luck.

   Alan
Beverley - 08 Sep 2006 20:19 GMT
I agree with Alan's comments. But the bottom line is if the cancer has
escaped the area then it has escaped and no amount of surgery +RT or RT or
combo RT's can do anything about it. To me it's a little like lost
luggage,;it gets packed in the belly of the plane and what happens to it
after that is anyone's guess. Most of the time it is right where you expect
it to be when you get off the plane. Sometimes they get lucky and find it
for you a few days later. And then there is the mystery of the totally lost
luggage...................
Bev

> > However if RRP fails, you can get a second chance doing RT to the
> > prostate area..
[quoted text clipped - 11 lines]
>
>     Alan
MAS - 09 Sep 2006 00:49 GMT
If primary treatment fails, then all primary treatments would have also
failed. This is from my Medical Oncologist. The reason has to do with
microfibers escaping and floating around for a place to dwell.

GD

>> However if RRP fails, you can get a second chance doing RT to the
>> prostate area..
[quoted text clipped - 11 lines]
>
>    Alan
Leonard Evens - 08 Sep 2006 17:28 GMT
> As I am trying to choose between RT and RP, I realized that I have
> heard of several MD's with PC that chose RT. I'm not saying that no MD
> has ever chosen RP, I've just not read anything about it.

There is a MD who has posted here from time to time.  He does radiology
of some sort and he is involved with diagnosis of prostate cancer but
does not treat it, if I remember correctly.   He was relatively young
when diagnosed with prostate cancer and after consulting various
experts, he chose surgery.  A radiation oncology even recommended it to
him over surgery.  One argument was that radiation leaves some prostate
tissue behind which in a relatively long life span could yield another
cancer.

> The one I remembered that really struck me was Dr. Charles "Snuffy"
> Myers. For those who don't know, he is a medical oncologist who has
[quoted text clipped - 25 lines]
> radiation are equal to or better than the best results reported for
> radical prostatectomy.

I think other experts would disagree strongly with that.  In particular,
Peter Scardino, in his book "The Prostate" recommends against
bracytherapy for any man with any additional risk factor such as one of
the Gleason compoents 4 or greater, a PSA greater than 10, etc.   For
such men, he thinks surgery or external radiation is a better choice.
Scardino is a surgeon, so you might feel he is biased, but he is also
one of the world's leading prostate cancer researchers.  He works with
others such as radiation oncologists and has been an author of hundreds
of papers on the subject.   I only found two possible references to C.
Myers and prostate cancer in Medline/Pubmed.

> For men with more aggressive cancers associated with a poor
> Gleason-related prognosis, a PSA over 10 ng/ml, a more extensive cancer
> in the prostate gland, or the presence of capsular penetration, 3-D
> conformal or IMRT combined with radioactive seed implantation currently
> offers results that are clearly superior to the best surgical
> approaches."

You have a case of dueling experts here, but I think Scardino's
qualifications clearly beat Myers's.

> Can anyone refute this logic?
>
> Thanks,
>
> John
JohnHace - 08 Sep 2006 20:49 GMT
> You have a case of dueling experts here, but I think Scardino's
> qualifications clearly beat Myers's.

I don't think there is any contradiction between the two. What I read
is that Scardino said surgery or XBRT is better for high risk then
seeds alone. This makes sense. Seeds alone will not handle
extra-capsular penetration.

But SI+IMRT will handle that problem. And that is what Myers is saying.
In fact, he feels SI+IMRT is superior to surgery.

Even Scardino says on p. 306, "For a small, aggressive tumor that may
have extended outside the prostate in a way that can be included in the
treatment field, radiation may offer a better chance for local cure
than surgery."

I think both experts agree.

Thanks,

John
I.P. Freely - 08 Sep 2006 20:58 GMT
>> You have a case of dueling experts here, but I think Scardino's
>> qualifications clearly beat Myers's.
[quoted text clipped - 6 lines]
> But SI+IMRT will handle that problem. And that is what Myers is saying.
> In fact, he feels SI+IMRT is superior to surgery.

I haven't the time or, presently, the motivation to look it up, but I'm
99% sure I read recently in one of our vaunted sources that combination
internal/external RT offers no advantage over single-mode RT. People
considering RT might want to research that one.

I.P.
Beverley - 09 Sep 2006 06:49 GMT
IP what the heck freaks you out over RT? It works! For someone who is so pro
RP you've been nailed with one of the worst side effects of RP. Which is
exactly why my husband wouldn't even consider RP. To him quality of life was
not peeing in diapers for the next 30 years. He was not about to chance it.
Since you've put in your years and are living off of retirement maybe that
doesn't mean that much to you but it does to my husband who still goes to
work everyday.

You are not supporting people. You plow in here and scare the crap out of
every newbie. You make half the men facing additional therapy fearful of
ADT/HT or RT. Do you enjoy doing that? Yes, there are side effects but a few
side effects is a small price to pay for what may be years of a quality
living. It's cancer! You've got it; they've got it, get over it! And just in
case you haven't noticed the RT/brachy guys have it done and we never see
them again because they go back to living their normal life. They have
erections, they are not incontinent, and to them this was just a speed bump
in their life.

Personally I think having a RP is nuts but I'm not saying that to every
person. Why would anyone want to subject himself to that surgery unless that
was the only thing available? But I do understand that personal choices do
matter. Some men just want the cancer out of their bodies as quickly as
possible and they are willing to risk everything for it. Have you ever heard
me actually condemn anyone for choosing RP?  No, And you won't. Everybody
needs to make their own decision.

It's obvious that I'm pro combo RT's. I stay out here to give brachy a
voice. I don't need to be here, my husband as an undetectable PSA, he has no
problems with his bowels, and everything else he does have problems with is
taken care of with a couple of pills. Not a bad trade off! We have normal
sex once and sometimes twice a week.

You know that we disagree and I do not want to start a war. I can't take
this off the newsgroup because you have hid your true identity and email
addy. And I'm sure you don't like me because I am a woman, and an outspoken
one at that. I wish you no harm. But yes, most rad-onc will tell you that
brachy with EBRT is the platinum treatment with much fewer side effects and
offers a better chance of a "cure" for many men.

Just try to be a little kinder and look over the fence with greater
compassion. There's a half dozen men on this NG that would probably be dead
or dying if they weren't on ADT. They are still enjoying their lives and
playing with grandchildren. Yes, their sex drive is shot but they don't
care, they are too busy smelling the roses or playing with the grandchildren
to worry about their sex drive.

I meant it when I said I was pleased you had a good PSA test as I do not
wish anyone any harm. Just, please, be a little more sensitive to other
people. Sometimes it is not what you say but how you say it. You are
articulate and could contribute much more to this newsgroup if you would
just think before you type!

The men who supported my husband on this NG when he chose brachy were all
RP'ers, and they are the same guys with whom I still converse and feel
deeply indebted. They were the ones that keep me sane though the whole
process. That is what a support group is supposed to be. Yes, we exchange
knowledge and information as it becomes available. It's a BTDT group! We are
not here to trash every treatment except for the one we chose.

Don't expect me to respond because I probably won't. I don't have the time
right now and I have no intentions continuing this conversation. It is
perfectly okay to disagree but you don't need to throw grenades!

Bev

> I haven't the time or, presently, the motivation to look it up, but I'm
> 99% sure I read recently in one of our vaunted sources that combination
> internal/external RT offers no advantage over single-mode RT. People
> considering RT might want to research that one.
>
> I.P.
alva36@gmail.com - 09 Sep 2006 15:15 GMT
> IP what the heck freaks you out over RT? It works! For someone who is so pro
> RP you've been nailed with one of the worst side effects of RP. Which is
[quoted text clipped - 5 lines]
>
>  
Beverley-

Well done!

-Gordy
dan - 09 Sep 2006 16:44 GMT
> Just try to be a little kinder and look over the fence with greater
> compassion. There's a half dozen men on this NG that would probably be
[quoted text clipped - 10 lines]
> articulate and could contribute much more to this newsgroup if you would
> just think before you type!

Beverly

Very well said, thank you

Dan

Signature

PSA = 2.2 , 03/05/2003
PSA = 7.92, 09/30/2004, @ 54
Biopsy, 11/10/2004, G9(5+4) (multiple cores) (6 of 8 cores positive), T1C
EBRT, 01-03/2005 @55
Casodex (daily), begin. 11/16/2004
Zoladex, 12/23/2004, 03/10/2005, 06/14/2005, 09/14/2005, 12/14/2005,
03/14/2006, 06/14/2006
PSA, 0.1, <0.1, <0.1, <0.1, <0.1, <0.1

Bob Anthony - 09 Sep 2006 17:45 GMT
Bev:

In all fairness to I.P., Dr. Scardino did mention in his book, The
Prostate, on pages 323, and 324 "There is no evidence that cancers are
cured more effectively with combined approaches. (Combination External
Beam and Brachytherapy) I believe he referred to it as a "belt and
suspenders" approach.
Now do not kill the messenger, (me). I think that is what I.P. was
referring to.

B.A.
I.P. Freely - 10 Sep 2006 22:45 GMT
> Bev:
>
[quoted text clipped - 5 lines]
> Now do not kill the messenger, (me). I think that is what I.P. was
> referring to.

Thanks. That was one of several sources in the books and medical
literature.

I.P.
tchtic@yahoo.com - 10 Sep 2006 01:49 GMT
> IP what the heck freaks you out over RT? It works! For someone who is so pro
> RP you've been nailed with one of the worst side effects of RP.

One?  IP has two. He is impotent and incontinent.

I didn't quite understand his and others enthusiasm for RP.   Sometimes
I wonder if cognitive dissonance is at play.  Their advocacy for their
treatment justifies their decision.

The thought that there was another choice, equally effective, with
significantly fewer side effects, is too much to endure, so they take
the only path left to them, they embrace their fears and become it.

That's a little pop-psych but that's what it looks like.

I can't imagine choosing a treatment that has that high a risk of
impotence and incontinence.  

-kh
ron - 10 Sep 2006 02:17 GMT
tchtic@yahoo.com wrote...snip...
> I didn't quite understand his and others enthusiasm for RP.   Sometimes
> I wonder if cognitive dissonance is at play.  Their advocacy for their
> treatment justifies their decision.
>
> The thought that there was another choice, equally effective,

kh...What is equally effective, SI+XBRT or XBRT?  If it's the former
that you are referring to, I'd agree; if it's the latter, please point
me to some data.

> with significantly fewer side effects,

The data I'm aware of suggests SEs are more or less comparable, can you
point me to some data that shows RT has fewer SEs?  Let's keep in mind
that RT doesn't fully ablate the prostate until you're (give or take)
24 months out from treatment, so the data needs to be collected at some
meaningful time beyond that...Best wishes and good health, ron

> is too much to endure, so they take
> the only path left to them, they embrace their fears and become it.

kh...
tchtic@yahoo.com - 10 Sep 2006 14:51 GMT
> kh...What is equally effective, SI+XBRT or XBRT?  If it's the former
> that you are referring to, I'd agree; if it's the latter, please point
> me to some data.

I formed my opinion from the "dummies" book, Walsh's book, and a couple
others, as well as the various websites and 1st person reports, like
Andy Groves and the stories on seedpods.   None of these will say
outright that one approach is better or worse or equal.

I was asymptomatic going in, no pain, pee'd like a firehose, no bumps
to the gloved finger, PSA 10.  They found 5% of 7 (4+3) in one of 12
needles after 2 biopsies.

Inova gave me the full court press, 8 months of Lupron, 25 sessions
with their IMRT robot, and Pd-103 seeds, the skewering handled by their
"name-doc".  This is "probably" as good as the best RP or Da Vinci.

But, who knows.

> The data I'm aware of suggests SEs are more or less comparable, can you
> point me to some data that shows RT has fewer SEs?  Let's keep in mind
> that RT doesn't fully ablate the prostate until you're (give or take)
> 24 months out from treatment, so the data needs to be collected at some
> meaningful time beyond that...Best wishes and good health, ron

Again, the books, papers, and websites skate around the side effects.
I think the question is one of gradations of quality, not, oh, 50% of
rad-grads experience some ED, or whatever the numbers are.

I certainly have some ED.  The point is the how much is some.

Without a prostate full of seminal fluid nagging me to "take care of
this", there just aren't the urges that were there a couple years ago.

When I'm with a woman and things are warming up, my guy works without
chemical assists.  He takes more to get going and definitely doesn't
work as well as before so some might call it "ED".

I've tried Vitamin-V and Cialis and both help but I can go, er, bare
too.

I can drink 20 ounces of water and sleep for 8 hours.  When I get up in
the morning, I *really* have to go.  The 20 steps to the bathroom is
almost impossible and the last couple feet, drops are starting to ooze
out.

You might call it stress incontinence.

If so, then yes, rad gave me both side effects but the quality isn't
the same as looking for sales of bulk diapers or pads, reading up on
valve or rod implants, or mainlining erection drugs.

I'm not saying that side effects should be the primary concern.  I
agree that a cure is more important.  I won't know if I am cured for
another year or two or longer. That's the nature of Rad.

However, I drive the highways around here everyday with nut-cases who
floor their SUVs and weave in and out of traffic, just like the
commercials taught them to.

I call that life-threatening.  So you take some risks in life. There
are no guarentees and we do the best we can.

A couple times, I have had second thoughts about the treatment.  The
softer erection even with Vitamin-V, just isn't the same.  It might not
be all-important to the gals but a guy can miss being really hard and
really "up there".

Ditto orgasms.  Dribbling a small amount of semen is not the same
experience as a full roaring delivery.

We do the best we can with what we have.  

-kh
Alex - 10 Sep 2006 03:16 GMT
>> IP what the heck freaks you out over RT? It works! For someone who is so
>> pro
[quoted text clipped - 16 lines]
>
> -kh

It's presumptuous to declare that another guy's choice of treatment is
wrong, much less to ascribe to some psychological weakness the reasons for
his choice.
There is no treatment that is "right" for all men. If there were, there
wouldn't be the wide diversity of opinions among expert physicians and
researchers, much less the wide range of options offered to us as patients.
Age, physical condition, perception of risk (death versus side effects,
"cutting it out" versus lack of pathology report with RT), anxiety about
surgery, etc., all play into the decision.
If the outcome is good -- few SEs, no mets, low PSA -- it's natural to feel
good about the choice. It's also helpful to share that with other men facing
a similar decision, because those of us who are newly diagnosed want to hear
from those who have gone down all of these paths before us.
And if it turns out not so well, we want to know that too.
KH can't imagine a guy choosing RP, with its "high risk" of impotence and
incontinence. Others might have a hard time imagining a guy choosing RT,
with its risks of radiation-induced impotence over time, rectal burning,
fecal incontinence, elimination of the option for salvage surgery, and so
on. Yet clearly RT was the right choice for KH.
Unfortunately, with this disease we all study like hell, figure the odds
that seem best to us, and then roll the dice, knowing that no choice we make
offers any real certainty. That sucks, but that's PCa.

Alex
tchtic@yahoo.com - 10 Sep 2006 16:18 GMT
> It's presumptuous to declare that another guy's choice of treatment is
> wrong, much less to ascribe to some psychological weakness the reasons for
> his choice.

Not that.  I'm not talking about the reasons for "the choice".  It's
the reasons for the advocacy after the fact.

It sure looks like, "those ladies doth protest too much".

> If the outcome is good -- few SEs, no mets, low PSA -- it's natural to feel
> good about the choice. It's also helpful to share that with other men facing
> a similar decision, because those of us who are newly diagnosed want to hear
> from those who have gone down all of these paths before us.

The strange part of RP-advocacy is in stating that RP's ED and
incontenence are minor
bothers but the SE of Rad or ADT are to be avoided at all costs.

> And if it turns out not so well, we want to know that too.
> KH can't imagine a guy choosing RP, with its "high risk" of impotence and
> incontinence. Others might have a hard time imagining a guy choosing RT,
> with its risks of radiation-induced impotence over time, rectal burning,
> fecal incontinence, elimination of the option for salvage surgery, and so
> on.

It's a matter of degree.   My radiation-induced impotence is what some
guys might call being over 40, 50, or 55.  I can "do it"; I just can't
"do it" two and three times a day for 20 or 30 minutes like when I was
younger, 30, 40.  But then I can't run two miles either.

According to the Rad-doc at Inova, rectal side effects were a real
concern, hitting a small precentage of the early EBRT patients.   Since
Inova upgraded to 3DCRT and now IMRT and they adopted their
anti-radiation diet program with the carefully scripted
stool softeners, they haven't had a single serious rectal injury.

Believe me, I followed their diet and instructions strictly.

> Yet clearly RT was the right choice for KH.

I don't know that.  With rad, you don't really know for years.

Of course, there're enough reports of RP treatment failure and mets
that RP'ers don't really know either.

-kh
I.P. Freely - 10 Sep 2006 23:02 GMT
> I didn't quite understand his and others enthusiasm for RP.
> Their advocacy for their treatment justifies their decision.

I don't advocate, have enthusiasm for, recommend, or advise against ANY
PC tx. I just present and provide links to facts I found during my own
literature searches.

> The thought that there was another choice, equally effective, with
> significantly fewer side effects

Please inform the medical field of that choice. It fails to appear in
any of the literature.

> I can't imagine choosing a treatment that has that high a risk of
> impotence and incontinence.  

All PC treatments have a significant risk of i and i; it's just a matter
of when and how dramatically the i's may strike -- quickly with RP, more
slowly with RT, and DRAMATICALLY if and when WW fails. Realize also that
many people rate those i's way down their QOL priority list. My RP has
had virtually no impact on my life beyond switching from boxers to briefs.

I.P.
Heather - 10 Sep 2006 04:20 GMT
>>> You are not supporting people. You plow in here and scare the crap
>>> out of every newbie. You make half the men facing additional therapy
[quoted text clipped - 3 lines]
>>> they've got it, get over it! Just try to be a little kinder and look
>>> over the fence with greater
compassion.

There's a half dozen men on this NG that would probably be dead
or dying if they weren't on ADT. They are still enjoying their lives and
playing with grandchildren. Yes, their sex drive is shot but they don't
care, they are too busy smelling the roses or playing with the
grandchildren to worry about their sex drive.<<<<
-------------------------------------------------------------------------

Very well said, Beverley.  That is what I have been trying to get across
to him for a long time.  My Ron has no choice in the matter of ADT with
a soaring PSA, so IP's rants on that (or any) subject are totally
ignored in this house.

As for not having a sex life, frankly I don't give one sweet damn!!  I
have a husband of 45 years who is ALIVE & WELL.....that is all that
matters.  And we take each day as it comes.....we don't dwell on the
negatives.

Thanks.....Heather
Steve Kramer - 10 Sep 2006 16:23 GMT
> Personally I think having a RP is nuts

Ouch.

> It's obvious that I'm pro combo RT's. I stay out here to give brachy a
> voice. I don't need to be here, my husband as an undetectable PSA, he has
[quoted text clipped - 3 lines]
> taken care of with a couple of pills. Not a bad trade off! We have normal
> sex once and sometimes twice a week.

And, to me, this is exactly the strength of anecdotal input.

Brachy has possible SEs.  Direct and indirect SEs can lead to short term
and/or long term loss of function of organs, nerves and other body parts.
It can lead to death.  But, George is a shining example that it can cure, or
at least significantly arrest, prostate cancer.  And, it can do so,
apparently, without significant lasting SEs.

Surgery has possible SEs.  Direct and indirect SEs can lead to short term
and/or long term loss of function of organs, nerves and other body parts.
It can lead to death.  But, most here regained functions they lost in the
short term and some have been here for more than a decade without rising
PSA.

Hormone Therapy has possible SEs.  Direct and indirect SEs can lead to short
term and/or long term fatique, loss of short term memory, organ damage, and
loss of sexual function or desire.

Personally, IP's SEs are important.  He is an example of what might happen,
even if it usually does not.  His RP experience is important, but only
anecdotally.

My anecdotal example is as one who had T3/Gleason 7/PSA 16 cancer, RRP, EBRT
and ADT.  This morning, I walked 5 miles in 1 hour and 15 minutes, up and
down Grade 3 hills.   Thiry minutes agao, I ran up 15 steps from my lower
level to get the door bell.  I think I can have sex; I just don't want to.
And, more than likely, my PSA is back below 0.1.  Mine is an example of what
might happen, even if it is better than average.

That is the strength of the NG.  That is it's purpose.

Signature

PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3cN0M0 Neg margins
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron 07/03 (1 mo) 8/03 (4 mo), 12/03, 4/04, 09/04, 01/05, 5/05, 10/05,
2/06, 6/06
PSA  .07 .05 .06 .09 .08 .132 .145
Casodex added daily 07/06
Non Illegitimi Carborundum

tchtic@yahoo.com - 20 Sep 2006 02:13 GMT
...

> Brachy has possible SEs.  Direct and indirect SEs can lead to short term
> and/or long term loss of function of organs, nerves and other body parts.
[quoted text clipped - 11 lines]
> term and/or long term fatique, loss of short term memory, organ damage, and
> loss of sexual function or desire.
...

Steve, the above is a disservice.    You've homogenized the side
effects until they are meaningless and equal.

While what you say is "true", it's not TRUE.  The side effects from
seeds and IMRT are *generally* mild compared to the side effects from
surgery.   There are certainly cases of IMRT and seeds gone bad where a
guy can't pee, has to be TURPed, has major problems with erections,
etc.  Those cases are not common.

My *opinion* is that the major problem with seeds and IMRT is that
there are no long term statistics.   The RCOG folks seem to have the
most data and their stats look good, although they might be cherry
picking their patients.

I *think* the side effects from IMRT and seeds are generally much less
than RP,  fewer and milder problems with incontinence and ED.  That's
certainly my experience and my experience matches what I've read in the
books.

No one gets off scott free but rad is close to a cake-walk as it gets.

The problem with rad isn't the business about "I need to see the path
report" or "I want to know what my margins were". That's a stalking
horse that some surgeon invented and we sheeple are echoing it.

If *knowing* were a concern, guys would be hollaring for Prostascint,
bone scans, and color doppler ultrascans before they started treatment.
Heck, if it really were a concern, someone would invent the retropubic
or robotic biopsy.

The problem with rad is you know up front that you won't know how you
did for 3 years or so.  You hope you're in the roughly 90% that ends up
cancer free.

With RP, you're pretty sure in a few months that you're OK, unless it
turns out that you're not.  You hope you're not in the roughly 10% that
has a recurrance.

Exactly why this is different, well, I can't explain that.

Then with RP there's the percentage where they wake you up and tell you
that the cancer was more extensive than orginally thought and they had
to take the nerves.

That would be incredibly disheartening.   I might be a little off on
this but while I was on Lupron and in the 6 months or so after, I had
to face the issue of impotence. It was very difficult.

I hoped that things would perk up as the Lupron faded and my T
increased but I didn't know if they would.   What if the ED was due to
radiation damage to the nerves, valves, or blood veins?  What if I
couldn't have or maintain an erection?

Those first seconds as you slide into a woman, the blood pounding in
your ears drowns out her quick gasp for breath.  What if I could never
experience that again?

As for hormones/ADT, that's a deal with the devil.  That's hardly a
choice.

-kh
Steve Kramer - 20 Sep 2006 02:30 GMT
> Steve, the above is a disservice.    You've homogenized the side
> effects until they are meaningless and equal.

Yeah.  That was my intent.  I find the bickering between treatments to be a
disservice and the claims of one over the other to be untrue.  Over time,
the potential and usual SEs probably do even out.

> While what you say is "true", it's not TRUE.  The side effects from
> seeds and IMRT are *generally* mild compared to the side effects from
> surgery.   There are certainly cases of IMRT and seeds gone bad where a
> guy can't pee, has to be TURPed, has major problems with erections,
> etc.  Those cases are not common.

I had RRP.  The side effects are as I described.  I had EBRT.  The side
effects are as I described.  I have no further to fear from RRP.  However, I
can expect the deterioration from EBRT to continue.

> No one gets off scott free but rad is close to a cake-walk as it gets.

In the short term, I have to agree.

> As for hormones/ADT, that's a deal with the devil.  That's hardly a
> choice.

Been there too.

Signature

PSA 16 10/17/2000 @ 46
Biopsy 11/01/2000 G7 (3+4), T2c
RRP 12/15/2000 G7 (3+4), T3cN0M0 Neg margins
PSA  .1  .1  .1  .27  .37  .75
EBRT 05-07/2002 @ 47
PSA  .34 .22 .15 .21 .32
Lupron 07/03 (1 mo) 8/03 (4 mo), 12/03, 4/04, 09/04, 01/05, 5/05, 10/05,
2/06, 6/06
PSA  .07 .05 .06 .09 .08 .132 .145
Casodex added daily 07/06
Non Illegitimi Carborundum

I.P. Freely - 10 Sep 2006 22:39 GMT
> IP what the heck freaks you out over RT?

Why do so many people attribute emotion (freaking out?) to facts? I just
don't get it.

> It works!

Never said, implied, or felt it doesn't.

> For someone who is so pro RP

I'm  not pro or con RP or RT, don't recommend one over the other.
They're comparable cures, as best as I can tell.

> you've been nailed with one of the worst side effects of RP.

That's your opinion; it's not mine. Some SEs are personal judgment calls.

> Which is exactly why my husband wouldn't even consider RP. To him quality
> of life was not peeing in diapers for the next 30 years. He was not
about to chance it.
> Since you've put in your years and are living off of retirement maybe that
> doesn't mean that much to you but it does to my husband who still goes to
> work everyday.

So? No one knows I wear pads if I don't tell them. Did you find pads a
big QOL issue for the 40-some years you wore them? Did you walk around
the office on big days in fear that someone might realize that -- GASP!
-- you were WEARING ABSORBENT ITEMS?

> You are not supporting people.

I'll let people making tx choices be the judge of that. They need all
the facts they can get, and as you and your husband have said, SEs are a
huge part -- potentially life-affecting in his case because they drove
his tx choice -- of that decision. The literature states and this forum
demonstrates almost daily that SEs are glossed over or altogether
ignored -- often until it's too late to go back -- by our oncologists.

> You plow in here and scare the crap out of every newbie.

So we should just let them choose treatments based on . . . what? Cost?
Convenience? Cure rates based on 15-year-old statistics? Whether our
cancer returns or not, what's its primary impact on our daily lives for
the next year or decade? SEs! What drove your husband's choice? SEs!
What drove the tx my rad onc prescribed for me? SEs!

> You make half the men facing additional therapy fearful of ADT/HT or RT.

No, FACTS make (rational) people fearful of cancer and its treatments. I
just quote 'em so interested pts can add them to their decision data
bases. We've all seen far too many cases right here in our minuscule
sample of what lack of SE knowledge can do to uninformed pts. I hope
EVERY pt and partner have a reasonable fear of ALL cancer treatments;
what else would motivate them to take it seriously, take the time to
investigate their options, choose an exceptional oncologist, and choose
their tx with the whole picture (cure rates and SEs) in mind.

> Yes, there are side effects but a few side effects is a small price
> to pay for what may be years of a quality living.

This contradicts your statement that your husband pinned his whole
future on his aversion to urinary incontinence.

> It's cancer! You've got it; they've got it, get over it! And just in
> case you haven't noticed the RT/brachy guys have it done and we never see
> them again because they go back to living their normal life. They have
> erections, they are not incontinent, and to them this was just a speed bump
> in their life.

Unless, of course, you actually count the ones who DIDN'T enjoy the
perfect picture you paint. Do you think surgery would still exist if
your statement were accurate?

> Personally I think having a RP is nuts

And you call ME biased? I don't think ANY mainstream tx is nuts. They're
OPTIONS, with choices to be made based on medical and personal facts and
opinions and preferences.

> but I'm not saying that to every person.

You just did.

> Why would anyone want to subject himself to that surgery unless that
> was the only thing available?

Your bias is showing again.

> But I do understand that personal choices do matter.

So why do you thus speak out so stridently against RP? You don't see me
recommending for RP or against RT or ADT.

> Have you ever heard me actually condemn anyone for choosing RP?

Nor I for RT or ADT?

> Everybody needs to make their own decision.

Exactly my entire point and my reason for being here. What good's a
cancer tx choice made without considering ALL the facts and
substantiated opinions available?

> And I'm sure you don't like me because I am a woman, and an outspoken
> one at that.

I'm sick and tired of people playing race or gender or ethnic cards
every time they run out of facts. My wife is a woman who built a career
out of waging entrenched battles with colonels and generals in the
Pentagon, about as chauvinist a place as exists in this country outside
a mosque, and I admire her for that and for the things she accomplished
there, including saving taxpayers many billions of dollars and
converting many of those chauvinist pigs to believers that women can be
their equals. i.e., Keep your BS personal attacks to to yourself.

> But yes, most rad-onc will tell you that
> brachy with EBRT is the platinum treatment with much fewer side effects and
> offers a better chance of a "cure" for many men.

The ASTRO disagrees with you. See
http://www.newswise.com/articles/view/502645/ .

> Just try to be a little kinder and look over the fence with greater
> compassion. There's a half dozen men on this NG that would probably be dead
> or dying if they weren't on ADT. They are still enjoying their lives and
> playing with grandchildren. Yes, their sex drive is shot but they don't
> care, they are too busy smelling the roses or playing with the grandchildren
> to worry about their sex drive.

So? That doesn't change any facts.

> Just, please, be a little more sensitive to other people.

If "being sensitive" means dispensing bogus information or hiding real
information so pts make decisions based on BS and/or just "feel better"
until reality sets in, no thanks. That's not "sensitive, it's cowardly.
One makes end-stage terminal cancer pts "feel better", 'cause that's all
we can do for them. Pts with a chance of cure or substantial relief
deserve better than that.

> Sometimes it is not what you say but how you say it.

Of course. We all have our own unique interpretations of and emotional
reactions to life's experiences. That's exactly why I just lay the facts
out there bare naked and let each person use it -- or not -- as they
wish; how on earth could anyone word a fact in such a way that every
unique PC pt would react to it in the same pleasant manner?

> You . . . could contribute much more to this newsgroup if you would
> just think before you type!

That presumes that I could think in the same manner as each reader, word
each fact so it would upset no reader, and sugar-coat all the bad stuff
associated with PC and its treatments . . . impossible on all counts.
Here's proof that doesn't work: I DO think, and often reread and edit,
before I hit SEND. The fallacy in your statement is that my objectives
are not the same as yours. Yours is to sugarcoat everything, make people
feel good, and push your favored treatments; mine are a) to provide and
reference facts which help people make sounder treatment choices and b)
to AVOID recommending any particular tx. You want people to choose RT
and/or ADT; I don't give a damn what tx they choose but want their
choice to be based on every fact and personal consideration they can
muster.

> They were the ones that keep me sane though the whole process.
> That is what a support group is supposed to be.

This has been discussed ad nauseum in this forum, without consensus.
Many, maybe most, of us want more than strokes from this group; they
want facts and opinions on which to base tx decisions, not "Oh, you'll
be fine. Just pursue this or that panacea and you'll still be playing
tennis at 120, your gas mileage will double, and your toilet will never
need to be flushed twice." Look at the thread topics; how many of them
say, "Please tell me my cancer will go away."?

> We are not here to trash every treatment except for the one we chose.

In my nearly two years here I have seen only one or two people trash any
tx other than drinking one's own urine; I certainly have never done so.
But what you do -- make up feel-good homilies about RT and ADT and
represent them as fact -- is at least as harmful because it leads to way
too many surprises, some reversible but some devastating.

> you don't need to throw grenades!

I feel SO sorry for people who equate facts with grenades. It may make
some of life's choices simple in the short term, but it all too often
blows up in our faces a short ways down the road.

Feel free to keep fabricating and dispensing your palliative
touchy-feely homilies, but don't expect the more responsible people here
to let them pass without a dose of reality. It's just not fair to people
who still have a chance at cure or long-term palliation. We WANT you
holding our hands in our deathbeds, but your homespun tx advice
interferes with those of us still trying to treat and defeat the bastard.

I.P.
Alan Meyer - 13 Sep 2006 03:20 GMT
> I haven't the time or, presently, the motivation to look it up, but I'm
> 99% sure I read recently in one of our vaunted sources that combination
> internal/external RT offers no advantage over single-mode RT. People
> considering RT might want to research that one.

I'm no expert myself, but a radiation oncologist whom I respect
told me this same thing.  He said that there is no proven difference
in outcomes for men receiving EBRT alone vs. EBRT combined
with brachytherapy.

When I pressed him as to which he recommended, he told me
that, although he couldn't justify one over the other based on
published outcomes, when his father-in-law developed prostate
cancer he treated him with EBRT + SI.

   Alan
I.P. Freely - 13 Sep 2006 04:01 GMT
>> I haven't the time or, presently, the motivation to look it up, but I'm
>> 99% sure I read recently in one of our vaunted sources that combination
[quoted text clipped - 10 lines]
> published outcomes, when his father-in-law developed prostate
> cancer he treated him with EBRT + SI.

Well, since I wrote that, it took only a few clicks to verify that ASTRO
sez all mainstream PC cures -- surgery, external rad, seeds, and
combination external/seeds - have virtually indistinguishable survival
records. The implication, if they're right? That just as the PCRI sez
about adjuvant tx, curable pts may as well choose their initial tx by
SEs rather than life span prognoses. Sorta places emphasis on accurate,
thorough, prior understanding of SEs and their treatment, doesn't it?

I.P.
Alan Meyer - 14 Sep 2006 02:55 GMT
...
> Well, since I wrote that, it took only a few clicks to verify that ASTRO
> sez all mainstream PC cures -- surgery, external rad, seeds, and
[quoted text clipped - 5 lines]
>
> I.P.

With a few caveats, I agree with that.  One caveat is that
brachytherapy, when used alone without EBRT, is NOT as
effective for intermediate or high risk patients as EBRT or
EBRT + brachytherapy.

Also, I'm not sure that the treatments really are exactly equal.
For example, it is conceivable to me that well done radiation
has a higher probability of a cure than well done surgery if the
cancer has penetrated the capsule.  And conversely, it is
conceivable to me that well done surgery has a higher
probability of a cure than well done radiation if the cancer
is completely organ confined.

But  this is just speculation on my part, and even if it were
true, I don't know what the difference in probabilities amount
to, or to what extent a patient can determine whether his
cancer is completely organ confined prior to actual surgery,
or how he can balance the chance that radiation might not
kill some cancer cells inside the prostate vs. surgery not
killing some outside.

Given all the uncertainties, it may well be that you might as
well try to avoid the side effects you fear most as do anything
else.  But also pick the best doctors you can find because
that really will influence your probability of a cure.

   Alan
ronju99 - 17 Sep 2006 03:19 GMT
The problem I have with all this is the comparison of results based upon
questionable studies. The results from confined cancer by surgery is
probably close to 100% if done properly. But radiation studies will use
surgeries that include marginal and questionable stages  that probably
shouldn't have been done in the first place that skews the surgery results
to some lower percentage for cures. By doing that they can claim similar
results. The problem is that there still isn't any long term studies on
radiation that extend out at least ten years or more. The studies they us
are speculative and flawed. If seeds or any other type of radiation was as
effective as surgery on confined cancer, they wouldn't have to keep coming
up with so-called better treatment options. Usually they end up using a
variety of hormone and radiation treatments in hopes that throwing
everything at it will kill all the cells. Unforunately they get a lot of
the good ones in the process. They never want there studies to go much
over five years as there resuults wouldn't look so good.

Ron S.
Alex - 17 Sep 2006 23:20 GMT
> The problem I have with all this is the comparison of results based upon
> questionable studies. The results from confined cancer by surgery is
[quoted text clipped - 13 lines]
>
> Ron S.

This seems like a wildly overbroad statement. According to you, all or a
large portion of radiation studies are "questionable" and wrongly compare
radiation to surgeries that "probably should not have been done in the first
place." But you don't say where you get that information, which if true
undermines the ethics and scientific credibility of a whole lot of doctors,
hospitals and professional journals.

You also say that if radiation or seeds had results as good as surgery,
"they wouldn't have to keep coming up with so-called better treatment
options." Huh? When has medical science declared, "hey, we got it right, so
there's no need to try to improve"? If that were the case, we'd still be
subjected to radical prostatectomies that didn't try to save nerves, or that
use robotic keyhole surgery for less blood loss and faster recovery.

Alex
ronju99 - 18 Sep 2006 19:27 GMT
Alex,
 With all due respect, reference one long term study of any radiation
treatment that supports the claim that the treatment is as good or better
than surgery.
 I believe that most people that research the internet don't really
appreciate how much they are exposed to marketing and that goes especially
true from the medical comunity. You want to believe it so therefore it must
be true.
 I believe that the best course for CONFINED prostate cancer is open RP.
The only other possible option would be Robotic LRP however due to it's
recent development there isn't any long term data to determine it's
effectiveness. I had what you call Keyhole surgery or LRP and wouldn't
recommend it for anyone. Yes, my case may have been unique but the leaning
curve is extremely difficult for surgeons especially for prostate surgery
and there is a big difference between perception and reality. Nerve
spareing can be done just as well if not more easily with open RP.
  What's usually best for a patient is spending the least time under
anesthesia and open surgery will usually accomplish that over the LRP and
RLRP. LRP being the longist in most cases.
  What disturbs me most is members telling newbies that they have many
options for treatment and all they have to do is researh and read and make
a decision and don't look back. I believe people come here for a reality
check. They know they can do the research. They are wanting to cut through
all the crapola.
  One needs to do a better job of defining the terms we use when we
communicate. Surgical removal of the prostate does NOT treat the cancer,
therefore it should not be included in the term treatment options. A
successful surgery will in now way compromise any cancer cells. Another
problem is calling the removal of the prostate a cure for prostate cancer.
Obviously if the cancer is removed along with the prostate then one should
not have anymore issues with prostate cancer. I don't call that a cure in
the medical sense.
 On the other hand, all other options available attempt to treat the
cancer cells by altering the DNA, freezing them, burning them or starving
them to death. These treatment options are used to manage the cancer with
the hope of buying a patient more time although there isn't any convincing
evidence that it does that very well.
 Remember, we are talking about early localize prostate cancer that at
our best guess is still confined to the prostate. The prostate is one of
the few organs that we can live without.
 Bottom line: Why would a person that is still relative young and healthy
pass up removal of the prostate with the cancer confined when there is NO
CURE for prostate cancer. Or are you telling me there is a cure for
prostate cancer and if so let everyone know because we can end the debate
now.

Ron S.
I.P. Freely - 18 Sep 2006 21:32 GMT
> reference one long term study of any radiation
> treatment that supports the claim that the treatment is as good or better
> than surgery.

Once again, see http://www.newswise.com/articles/view/502645/
Excerpts include:

Cure rates are just about equal for prostate cancer patients treated
with surgery, radiation, permanent seed implants and permanent seed
implants combined with radiation therapy, according to a new study in
the January 2004 issue of the International Journal of Radiation
Oncology·Biology·Physics, the official journal of ASTRO, the American
Society for Therapeutic Radiology and Oncology.

The study included 2,991 consecutively treated patients

“This study represents the largest published series comparing the most
frequently used therapies for patients with clinically localized
prostate