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

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Naaman - 06 Mar 2006 16:58 GMT
Two months ago, my urologist called to tell  me that my prostate biopsy
had revealed a tiny bit of cancer and  that he wanted to talk face to
face with me and my wife.

Malignancy indicated in about 10 percent of one of 12 cores taken. "Very
 early stage" according to urologist.
Gleason 6,t1c, PSA 4.5. Oh, yes, I'm 72 and good health otherwise,
except for a bad shoulder that is going to have to be scoped before I
can get back on the golf course.

I was told I am a good candidate for radical prostatectomy, radiation or
cryotherapy. Have talked with two friends who 1. had RP and 2. had seed
implants. Both consider their treatments a success after 10 or more
years. Next step is another PSA in another month, which may be decision
time, depending on the outcome.

I've been doing lots of on line research, but there seems to be a
paucity of current information on long-term studies relating to success,
or failure, of the various treatment methods--or perhaps I'm just
missing them.

Anyway, advice, suggestions, comments, etc. welcomed.

Naaman Nickell
Steve Jordan - 06 Mar 2006 17:27 GMT
On March 6, Naaman wrote, in pertinent part:
> Two months ago, my urologist called to tell  me that my prostate
> biopsy had revealed a tiny bit of cancer and  that he wanted to talk
[quoted text clipped - 16 lines]
> success, or failure, of the various treatment methods--or perhaps I'm
> just missing them.
Welcome to the club no one wants to join.

It does appear, based upon the biopsy (which is not 100% reliable;
nothing is) that the case is indeed in its early stage.

Further than online research, I recommend:

1. Discussion of the case with a radiation oncologist, as the uro is not
likely to be fully up to date regarding radiation treatment (tx).

2. Referral to the website of the Prostate Cancer Research Institute at:
http://prostate-cancer.org/index.html
It includes a large amount of reliable and objective information.

3. Read, study, the premier book on prostate cancer (PCa), _A Primer on
Prostate Cancer_ subtitled "The Empowered Patient's Guide," by
oncologist and PCa specialist Stephen B. Strum, MD and Donna Pogliano,
PCa warrior. It is available via Amazon, UsToo International, and the
PCRI, as well as other relevant sources. It too is reliable and objective.

Once all the information on the disease and its tx is in hand, an
informed judgment can be made as to the best tx for this particular
tumor. They are all different, which is why anecdotes about someone's tx
and result, though interesting and of some limited utility, must not be
relied upon as a definitive guide to a tx regimen.

Best of luck. Please keep us informed.

Regards,

Steve J

"We must tailor the treatment to the nature of the disease. We must
listen to the biology."
-- Stephen B. Strum, MD
Naaman - 06 Mar 2006 17:40 GMT
> On March 6, Naaman wrote, in pertinent part:
>> Two months ago, my urologist called to tell  me that my prostate
[quoted text clipped - 52 lines]
> listen to the biology."
> -- Stephen B. Strum, MD

Thanks for the info and advice. I do take anecdotal information simply
as one person's experience, although it may be useful at the margin.

I gather bottom posting (no pun intended) if the preferred style here.

Naaman
Steve Jordan - 06 Mar 2006 17:57 GMT
On March 6, Naaman responded to me:

(snip)
> Thanks for the info and advice. I do take anecdotal information simply
> as one person's experience, although it may be useful at the margin.
Glad to help.
> I gather bottom posting (no pun intended) if the preferred style here.

Actually, posting in line (aka "bottom posting") is the method  that
most closely resembles the way people converse. Top-posting is
backwards, sometimes difficult to follow, and is often simply deleted
without reading.

In line posting is, IMO, courteous and does not waste one's time. But
the poster should snip matter that is not relevant to what (s)he has to
say. That, too, is courteous.

Believe it or not, there are etiquette guidelines. See, for example,
http://www.river.com/users/share/etiquette/

Some folks deliberately refuse to follow the guidelines for what I
suppose they think are good reasons.

Regards,

Steve J
Naaman - 06 Mar 2006 18:37 GMT
> On March 6, Naaman responded to me:
>
[quoted text clipped - 22 lines]
>
> Steve J

This is drifting OT, so I'll keep it short. I've be hanging around
message boards since the days of FidoNet, so I've been embroiled in my
share of etiquette discussions--and flame wars. I just try to go along
with the culture of the newsgroup now.

Naaman
Steve Kramer - 06 Mar 2006 22:38 GMT
> This is drifting OT, so I'll keep it short. I've be hanging around message
> boards since the days of FidoNet, so I've been embroiled in my share of
> etiquette discussions--and flame wars. I just try to go along with the
> culture of the newsgroup now.

I was a poster on FidoNet and frequent flier on OneNet and other BBSs.  I
think you will find here a unique situation.  Whereas we will occasionally
have a heated discussion, usually of OT subjects, flamers are rare and often
find haven elsewhere.
I.P. Freely - 07 Mar 2006 20:23 GMT
> I've been embroiled in my share of ... flame wars.

Then you'll be glad to note that they are almost non-existent here. Even
when we disagree strongly, unsupported ad hominem or sniping is rare and
usually short-lived in this group. I'd have to guess that age and its
implied maturity is a factor, because that's almost the only common
factor here unless having PC in the family IMPROVES behavior.

I.P.
Alan Meyer - 08 Mar 2006 06:40 GMT
>> I've been embroiled in my share of ... flame wars.
>
> Then you'll be glad to note that they are almost non-existent here. Even when we
> disagree strongly, unsupported ad hominem or sniping is rare and usually short-lived in
> this group. I'd have to guess that age and its implied maturity is a factor, because
> that's almost the only common factor here ...

There does indeed seem to be an inverse correlation of age
with flaming in newsgroups.  I've noticed that flaming seems
much heavier in the newsgroups frequented by young people.

> ...  unless having PC in the family IMPROVES behavior.
>
> I.P.

Perhaps us folks who have had cancer have discovered, if we
didn't already know it, that life is too short and too precious, to
be wasted on flame wars.

   Alan
Steve Kramer - 06 Mar 2006 22:24 GMT
> On March 6, Naaman responded to me:

> In line posting is, IMO, courteous and does not waste one's time. But the
> poster should snip matter that is not relevant to what (s)he has to say.
[quoted text clipped - 5 lines]
> Some folks deliberately refuse to follow the guidelines for what I suppose
> they think are good reasons.

Being one of those, I sincerely apologize.  I will, as long as I remember to
do so, respond in-line forever more.
I.P. Freely - 07 Mar 2006 20:14 GMT
> I gather bottom posting (no pun intended) is the preferred style here.

IF it's preceded by careful elimination of irrelevant pony pucky. Ponies
we like; having to scroll through pucky to find the pony may send busy
readers on to greener pastures.

I.P.
Bob Anthony - 06 Mar 2006 20:55 GMT
Well it goes to prove that both of your friends have done very well with
their decided treatments. I think it can be said that both treatments,
surgery and radiation, have improved over the last 10 years. Steve is
correct in pointing you in the direction of reading books written by
experts/doctors before committing to an actual treatment. The advice and
information that can be obtained here can be very valuable to you as
well, but it is good to educate yourself and then join discussions here.
You will find the personal experiences by the members and advice that
can be offered by some very smart people who share one thing in common,
very enlightening. My personal advice is to find a doctor who
specializes in the treatment of this particular disease. This seems like
an obvious thing to do but I'm constantly surprised that some people do
not interview more than one doctor. After quizzing my first uro, I came
to the conclusion although he was a good doctor, he lacked the surgical
experience and expertise in PCa for me to feel confident about him
actually operating on ME.

B.A.
Alan Meyer - 06 Mar 2006 21:23 GMT
> Two months ago, my urologist called to tell  me that my prostate biopsy had revealed a
> tiny bit of cancer and  that he wanted to talk face to face with me and my wife.
[quoted text clipped - 16 lines]
>
> Naaman Nickell

I agree with the other posters that you should do some research on all
this using the books and websites mentioned.

Another alternative that your urologist didn't mention was "watchful
waiting".  It may be that you have a very indolent cancer that isn't
growing fast enough to ever be a danger to you.  So one possible
course of action is to insure that your lifestyle and nutrition are as
positive as possible - for example, lycopene, vitamin D, selenium,
ibuprofen, and maybe vitamin E have all been shown to have
_possible_ (not fully proven) benefit.  And conversely, reduce fat
in your diet, etc.

With watchful waiting you need to emphasize the "watchful" part,
with regular PSA tests, perhaps every 3 months or so, to be sure
that the cancer isn't going anywhere.

If I were you in your situation, and I decided on treatment, I think
I'd go for brachytherapy - implanted seed radiation.  As compared
to surgery or external beam radiation, it confines the damage to
a relatively small area and hence has relatively fewer side effects
(though there are no guarantees!), it can be done very quickly,
typically with a hospital procedure and an overnight stay, and
unless something goes wrong (again no guarantees), you'll be
on your feet again and back to normal life in a few days - though
you will probably experience urinary difficulties for some months
after the procedure.

Brachytherapy is not the best treatment for serious cases, but is
said to be highly effective in early, low grade cases like yours.

Also, if I decided on treatment, I'd want a good doctor - one
who has treated a lot of prostate cancer (not, for example a
urologist that specializes in female incontinence, or a radiation
oncologist that specializes in breast cancer), and one who
listens, answers questions, takes his time, and sounds concerned
and intelligent.

However, my opinion is worth what you're paying for it.  See a
radiation oncologist for professional advice on brachytherapy,
and discuss watchful waiting with him and your urologist.

Best of luck.

   Alan
Steve Kramer - 06 Mar 2006 22:12 GMT
Welcome, Naaman!

> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to face
> with me and my wife.

I can still remember that call, where I was sitting, and what I was looking
out at from my office.

> Malignancy indicated in about 10 percent of one of 12 cores taken. "Very
> early stage" according to urologist.
> Gleason 6,t1c, PSA 4.5. Oh, yes, I'm 72 and good health otherwise,

I would not categorize it as "very" early, but it is certainly early enough
to opt for surgery.  There are two major criteria for choosing surgery or
radiation.

One is age.  And, frankly, at 72, you would often be outside the window.
But, if you are in good health and able to handle major abdominal surgery,
then you have the option.

Two is Gleason.  At G6, you are in great shape for surgery.  Your T1c would
also seem to support the G6, but then DREs are maybe 33% to 50% accurate in
determining stage and biopsies can be off about 20% of the time.

I'd say you have two very viable options.

> I was told I am a good candidate for radical prostatectomy, radiation or
> cryotherapy.

Several people among us have tried Cryo.  Only one, Dan Dubosky, has been
thus far successful (how's that, Dan?)

> I've been doing lots of on line research, but there seems to be a paucity
> of current information on long-term studies relating to success, or
> failure, of the various treatment methods--or perhaps I'm just missing
> them.

www.phoenix5.org or cancer books by Walsh, Strumm and Scardino are great
resources.  What you will find is that there is a long history on surgery
results, a short history on radiation results, and a really short history on
cryo results.  Surgery advocates claim superiority.  Radiation advocates
claim results similar to surgery.  I'm not sure if I've seen cryo advocates
here or in my research.

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
PSA  .07 .05 .06 .09 .08 .132
Non Illegitimi Carborundum

Alex - 07 Mar 2006 00:48 GMT
"Steve Kramer" <skramer@cinci.rr.com> wrote
[ Snip ]
> cryo results.  Surgery advocates claim superiority.  Radiation advocates
> claim results similar to surgery.  I'm not sure if I've seen cryo
> advocates here or in my research.

Steve,

I met with Dr. Duke Bahn a couple of weeks ago, and he has a journal article
about to be published on the effectiveness of cryo, based on a significant
number of patients.

He's an advocate of cryo for appropriate cases, and even of freezing only
one lobe of the gland for very localized cancers. (Cryo almost inevitably
clobbers the nerves controlling erection, since they are adjacent to the
prostate gland and wind up getting frozen as well. By freezing only one
lobe, the nerves on the other side are spared. Of course, so is any prostate
cancer that might be hidden away there.)

Alex
Dan Dubosky - 07 Mar 2006 15:22 GMT
> Several people among us have tried Cryo.  Only one, Dan Dubosky, has been
> thus far successful (how's that, Dan?)

Very good, Steve :-).  But I am only 6 months post-op with cryo and looking
forward to my next PSA check in about a month.  So I'm not sure that anyone
should base their decision on my case.  The jury is still out.

Dan
Steve Kramer - 08 Mar 2006 00:28 GMT
>> Several people among us have tried Cryo.  Only one, Dan Dubosky, has been
>> thus far successful (how's that, Dan?)
>
> Very good, Steve :-).  But I am only 6 months post-op with cryo and
> looking forward to my next PSA check in about a month.  So I'm not sure
> that anyone should base their decision on my case.  The jury is still out.

I agree that it's too early to base a decision, let alone too unique, but as
far as your comfort zone is concerned, you have already made it longer than
the others without indications of failure.  I like your chances.
MH - 07 Mar 2006 03:48 GMT
My father chose brachytherapy at your age.... and six years later he's doing
fine!  Each treatment has it's pros and cons.... Just research them
carefully and read all you can.... and decide what you think is best *for
you*... and then never look back!

I wish you well!
MikeH

> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to face
[quoted text clipped - 20 lines]
>
> Naaman Nickell
Leonard Evens - 07 Mar 2006 04:30 GMT
> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 20 lines]
>
> Naaman Nickell

Try the Sloan Kettering website

www.mskcc.org/mskcc/html/10088.cfm

They only give 5 year biochemical failure rates based on pretreatment
criteria.  But if you keep in mind that it takes quite a while after
biochemical failure for the development of clinical symptoms, that may
be enough to get started.

In fact, with your statistics, you stand an extremely good chance of
being cured for all practical purposes by either surgery or radiation.
At your age, it is easier to avoid impotence with radiation that with
surgery.  Keep in mind, in any case, that impotence can be treated and
need not mean the end of your sex life.  I've never been convinced that
brachytherapy has any advantages over external radiation, but if only
the former is available to you, I don't see any reason not to choose it.

Cryotherapy has not had a good repuation generally, and that seems
confirmed by the anecdotal evidence reported here.  The people who've
used it don't seem to have had good experiences.
Alan Meyer - 07 Mar 2006 15:50 GMT
> ... I've never been convinced that
> brachytherapy has any advantages over external radiation, but if only
> the former is available to you, I don't see any reason not to choose it.
> ...

As I understand it from my layman's perspective, external beam
radiation (EBRT) or EBRT + brachytherapy, is more effective against
intermediate and high risk cancers than brachytherapy alone.  I don't
know why that is but speculate that it is easier for the radiation
oncologist to drench every part of the prostate with EBRT than with
brachy, and it also treats the area immediately around the prostate.

However the statistics for low risk cases (PSA < 10, G <= 6) are
just about as good for brachy as for anything else.  It does deliver
a very high cumulative dose of radiation directly to the prostate,
actually greater than the dose delivered by EBRT.

The big advantages have to do with the mode of treatment.  With
brachytherapy the clinical treatment takes a few hours as compared
to a few hours plus a small amount of time every weekday for 9 weeks.
Also, with brachytherapy I believe the radiation delivered to sensitive
structures outside the prostate like the rectum and bladder is less.

The disadvantage is that it is a surgical procedure.  It's not major
surgery like prostatectomy.  The body is never cut open.  But
needles are inserted through the perineum, anaesthesia is used,
and there is some soreness, and possibly some bleeding, afterward.

I've had both brachytherapy and external beam.  The EBRT was
certainly easier to do since there was no hospital stay and no
anaesthesia.  But the brachytherapy was over quicker and other
than some soreness that tapered off after a week, there was no
real pain.

   Alan
Jamie - 07 Mar 2006 21:39 GMT
> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 20 lines]
>
> Naaman Nickell
Jamie - 07 Mar 2006 21:42 GMT
Your situation is very similar to mine.  I was diagnosed in December
with a PSA of 6.2 and a Gleason of 6.  I researched on line and read
many books and conluded the any treatment option was worse than the
disease.  That said, I have opted for Brachytherapy (i.e. radioactive
seeds) and am scheduled for March 16th.  THere is a good book I am
presently reading on surviving prostrate cancer without surgery.  If
you want the title email me and I will bring it to work so I can give
you that information.

I wish you the best in what is truly a difficult decision.

Jamie

> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 20 lines]
>
> Naaman Nickell
I.P. Freely - 07 Mar 2006 22:22 GMT
>   I researched on line and read
> many books and conluded the any treatment option was worse than the
> disease.

What on earth are you reading? Where did you read that dying with bone
cancer in one's 50s over a period of months, maybe even years, is
preferable to another 15 years -- maybe 30-40 years -- of tennis, golf,
fishing, robust living, loving, etc.?

I.P.
Bob Anthony - 08 Mar 2006 00:37 GMT
I.P.

It's a book that is written by Bradley Hennenfent. It begins with a
misguided RP patient blowing the testicles off of his uro because he
(the patient) felt like an android and was in pain all of the time due
to the botched RP. Sounds like a bad sequel to an Arnold Schwartzenegger
movie. My opinion is that the book sounds more like science fiction than
fact. But what do I know, just my opinion.

B.A.
I.P. Freely - 08 Mar 2006 04:17 GMT
> I.P.
>
[quoted text clipped - 4 lines]
> movie. My opinion is that the book sounds more like science fiction than
> fact.

Sci fi ... and maybe paranoia, ignorance, fatalism, arrogance (in
advising others to  believe it), probably not having seen anyone die of
bone cancer, and the failure to believe that anyone has ever been cured
of PC. That single statement is enough for me to ignore anything else
the man has written, and Jamie would do well to keep reading, if indeed
"any treatment option was worse than the disease" represents
Hennenfent's philosophy.

I.P.
Ed Friedman - 07 Mar 2006 23:13 GMT
> Your situation is very similar to mine.  I was diagnosed in December
> with a PSA of 6.2 and a Gleason of 6.  I researched on line and read
> many books and conluded the any treatment option was worse than the
> disease.  

Jamie,

Have you checked out articles at:

http://www.prostateweb.com/pdfs/ASCO_PCF_02_2005.pdf

and

http://www.prostateweb.com/docs/HDTRT9.doc

They clearly show that treatment options exist which result in a quality
of life higher than what you had before being diagnosed with prostate
cancer.  The downside is that the treatment offers no chance for a cure.
 The upside is that the treatment has almost no chance of dying from
prostate cancer for men who start it at an early stage (T1-T3).

Ed Friedman
Naaman - 08 Mar 2006 17:55 GMT
I want to thank all of you who have taken time to weigh in here with
suggestions, advice, recommendations and your experiences. I see I still
have a lot of research and consultation to do.

Just visited my family doctor for another problem today and asked for
past PSA scores, which were: 3/1/03, 2.6; 9/16/04, 3.4; 3/17/05, 3.8;
10/11/06, 4.5, which was when he sent to to the urologist. I think there
are a couple of scores missing in the series, but the trend  is obvious.
Oh, the free psa on my final test was 15.1.

Again, thanks to all of you.

Naaman
Leonard Evens - 08 Mar 2006 22:48 GMT
> I want to thank all of you who have taken time to weigh in here with
> suggestions, advice, recommendations and your experiences. I see I still
[quoted text clipped - 5 lines]
> are a couple of scores missing in the series, but the trend  is obvious.
> Oh, the free psa on my final test was 15.1.

Your trend was very similar to mine.  In my case, I had to point out to
my doctor what the trend was, and he then sent me to a urologist.  In
his favor, he picked out one of the best urologists in the area.

I never had a free PSA test.

You are just barely in the range where PSA velocity suggests a biopsy.

In my case, it turned out I had a Gleason 7=3+4 cancer in four of six
samples (out of 12) on one side.  I had an RP and five years later my
PSAs are undetectable, I am not incontinent, and my erections more or
less returned (with a little help from Viagra) after about 18 months.

I think that if I had seen a urologist after the first jump in PSA, it
is possible my Gleason would have been a 6, and my chances might have
been marginally better, but I'm not complaining.

> Again, thanks to all of you.
>
> Naaman
Bob Anthony - 09 Mar 2006 01:42 GMT
Leonard:

A few questions. I had a psa test done during a kidney stone ailment a
few years ago which started me on this road. The uro included a psa test
and decided that my psa results was too high for a man of 52 at that
time and suggested a biopsy be done. My psa climbed almost a point the
year before, but the my GP back then did not say anything was wrong to
me. I had absolutely no knowledge of pc at the time, except to get
tested annually along with DRE's. I thought that the uro was nuts and I
waited to get retested before agreeing to a biopsy. (Sounds dumb now, I
know). I had a 3.x value, neg DRE and then 9 month later it came back as
7.x. Still nothing felt on the DRE. I had the biopsy done, by the uro I
thought was nuts, and it tuned out to be T1c with a Gleason 6 cancer.
Went through RLRP by a prostate cancer specialist (not the first uro who
did the biopsy) and the cancer was contained, negative margins, no
seminal vesicle involvment and good pathology overall. My psa after 15
months is still <0.1, but the Gleason went from a 6 at biopsy to a 4+3
at pathology. Could my Gleason have been a 6 nine months prior to the
surgery? Also, could the rapid rise suggest more trouble ahead? So far,
so good now, but I'm hoping that by not moving faster that I did not
screw myself. I know that the 2.0 + rise can mean a much poorer
prognosis according to some studies..

B.A.
ron - 09 Mar 2006 02:09 GMT
Hi Bob...I hope you don't mind me chiming in.  Where both your biopsy
and pathology specimens read by the same lab?  If they were read by
different labs they could have been graded differently even if they
were, in fact, identical.  Even if they were analyzed by the same lab,
grading error is still a possibility.

Several studies using repeat biopsies on men deferring treatment have
found changes in GS over time.  Here is one example of the timeframe
involved:
"Thirty-five percent (14/40) of the patients showed an increase in
biopsy grade to Gleason 7 or greater. Three progressed to Gleason 7
within 2 years, 4 progressed between 2 and 4 years, and 7 progressed at
greater than 4 years from initial diagnosis"

This same study found no correlation between those men whose PSA
increased >2ng/ml prior to the repeat biopsy and those men whose GS
increased to 7.  However, as you note, there appears to be some
correlation between PSA velocity prior to treatment and treatment
outcome...Ron
Bob Anthony - 09 Mar 2006 05:45 GMT
Hi Ron:

No problem with your chiming in at all. Leonard just gave me some food
for thought. No, the biopsy slides and pathology results after RLRP were
read by two different labs. I ultimately had the surgery done at the
Cleveland Clinic, and they had their own pathology lab there to read the
pathology results. The biopsy slides were sent to the Cleveland Clinic
before the RLRP, at the request of my new urologist/surgeon, for them to
view. They concurred, as far as I know, with the Gleason 6 on the
slides. It was only after the RLRP that the increase to G7 by was
reported by pathology. Hopefully I pulled the trigger early enough to do
some good. My surgeon did not appear, to me at least, to be very
concerned about the PSA velocity prior to my surgery. I guess only time
will tell, but I do think of the possibility of my not reacting fast
enough prior to the PSA jump. Nothing I can do about that now.

B.A.
Leonard Evens - 09 Mar 2006 16:45 GMT
> Hi Ron:
>
[quoted text clipped - 13 lines]
>
> B.A.

Another thing to keep in mind is that the research in PSA change > 2.0
the year before surgery is fairly recent.   Also,  PSA can increase for
a variety of other reasons, even if you do have prostate cancer.   As
ron pointed out, it is not unusual for the pathological Gleason (after
surgery) to be higher than the diagnositc Gleason based on biopsy.  I
suspect the reason your surgeon was not too concerned about the PSA
increase the year before surgery was the generally encouraging pathology
results following surgery.
Leonard Evens - 09 Mar 2006 16:38 GMT
> Leonard:
>
[quoted text clipped - 20 lines]
>
> B.A.

I see ron has already responded with more information than I have.  But
i think the upshot is that it is not possible to know such things with
any degree of confidence.  One may wonder about how things might have
gone differently as a matter of intellectural curiosity, but it is
fruitless to get too concerned about it.

I think the relevant question is whether our primary care doctors have
behaved properly.   I think they probably did.  It should be remembered
that things look different to urologists than they do to general
practitioners.  The urologist sees a signficant number of cases where
had the cancer been caught earlier, treatment might have been effective.
 The urologist was also more aware of early research suggesting that
PSA limits be lowered, particularly for younger men.   The primary care
physician, on the other hand, has seen lots of cases of men with
increases in PSA that didn't mean anything, and he may be reluctant to
refer for a biopsy without following the patient further.
Alan Meyer - 12 Mar 2006 20:58 GMT
>> ... My psa climbed almost a point the year before, but the my GP back then did not say
>> anything was wrong to me. ...
...
> ...  It should be remembered that things look different to urologists than they do to
> general practitioners. ...

My impression of general practitioners is that they deal with
such an incredibly wide range of ailments that it would take
a really exceptional one to have deep knowledge of specific
diseases.

I know that my GP may have people walk in to his office with
an injured foot, a sore throat, itchy scalp, or a sore in the mouth.
Then someone comes in with AIDS.  Then a pregnant young
girl.  Then a depressed person.  Then someone who has been
nauseous for three days.  Then someone with a rapid heartbeat,
or insomnia, or a twitch in the eyelid, or intestinal parasites, and
on and on.

When I told my doctor that the latest research indicates that
different PSA values are appropriate for different ages, he
said he didn't know that.  He thought 4.0 was the cutoff.  Before
that it's okay.  After that, see a specialist.  Nobody had referred
me to anyone when my PSA was 3.7 or thought there was anything
to think about at all.  It was in the normal range.

   Alan
Steve Kramer - 08 Mar 2006 23:46 GMT
> I want to thank all of you who have taken time to weigh in here with
> suggestions, advice, recommendations and your experiences. I see I still
> have a lot of research and consultation to do.
>
> Just visited my family doctor for another problem today and asked for past
> PSA scores, which were:

3/1/03, 2.6;
9/16/04, 3.4;
3/17/05, 3.8;
10/11/06, 4.5,

Assuming your doc saw the 2.4 and had you come in every 6 months thereafter
and waited to see 3 successive rises, he done you good.  Your graph looks
like the typical PCA curve.  Your doubling rate is > 24 months, if I read it
right.

These are all very good signs.

Disclaimer:  I am not a doctor, so my opinion doesn't mean squat.
woody - 08 Mar 2006 19:58 GMT
hi. I had a radical surgery when I was fifty. psa 3.7, gleason 6.  It
was the best decision I've ever made.  long period of recovery because
of major surgery - but once the cancer is out you'll never have to
worry again.  your psa isn't all too high considering your age.  if you
are a strong man, physically, then go ahead and have the
surgery--otherwise consider the seeds, radiation lastly.
Thomas Gentles - 18 Mar 2006 22:08 GMT
Hi Naaman

You might consider just waiting. My case is similar to yours. I
was diagnosed in 1997. Age 71. PSA 7.6. Gleason 6.

I was told that I needed an operation or radiation. After a lot of
study I opted for a natural health program instead. Diet,
exercise, supplements, life style and a few other odds and ends.

It's not an onerous program. For example the diet includes lots of
meat, fat, fruit, vegetables.  Red wine - not a lot - just a
couple of glasses a day. Just about anything as long as it's a
natural food. The other activities are on a similar theme.

I'm still waiting after nine years. My health is better than It's
ever been. Bexause of the health progrom. No symptoms of PCa. I've
now turned 80. My PSA in January was 4.5.

I can send you complete details of what I do and the complete
history of PSA readings etc if you think you might consider this
alternative.

Whatever you decide I wish you the very best.

Tom

>Two months ago, my urologist called to tell  me that my prostate biopsy
>had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 7 lines]
>.............................
>Naaman Nickell
paul - 19 Mar 2006 19:36 GMT
> I can send you complete details of what I do and the complete
> history of PSA readings etc if you think you might consider this
> alternative.

Tom:

Congratulations on 80 years!

Please post your information and lifestyle here for the benefit of all
who read this list. Each of the "brothers" have had their lives altered
in some way in dealing with the "Beast" within, and all have considered
WW at some point. Let us know what changes you made that may have
contributed to your sucess to now. We may not readily adopt your
lifestyle but we ARE interested in hearing from you.

Paul
Thomas Gentles - 21 Mar 2006 18:12 GMT
Hi Paul

Thank you very much for your congrats and suggestion that I post
those details on natural health.

One little problem. I ask your advise. Although the methodology
I've chosen to decide what leads to natural health is very simple
it does take a bit of explaining to, hopefully, increase the
understanding.

When I'm asked to talk on the subject I ask for a full hour. I've
tried to really reduce my notes in the last couple days. I've got
them down to six pages.

The one page chart I mention is on a Word file. Can a chart be
included in a posting???

I'd be delighted to mail a copy to anyone interested. But I need
your advice on whether a six page letter should be posted here.
Perhaps I could e-mail you a copy and then you could advise me????

Best regards
Tom

On Sun, 19 Mar 2006 paul wrote

>> I can send you complete details of what I do and the complete
>> history of PSA readings etc if you think you might consider this
>> alternative.
>
>Tom:

>Please post your information and lifestyle here for the benefit of all
>who read this list. ......
juniper - 22 Mar 2006 02:58 GMT
Tom,

You would have to post it as text.  I suggest you make a new
descriptive topic, like "my watchful waiting plan-- very long" and post
it that way.  I am sure many people over time will be grateful for the
information.  Uh, since there is an 'issue' going on in this group
right now with a hair-of-newt guy, and you don't want to be painted
with that brush, why don't you also include at the beginning your
original information.  About your PCa diagnosis, etc.  So that it is
clear you are talking about a valid case of PCa and that this is the
thoughtful approach to treatment you chose.

You could also post a summary, too, but it sounds like the information
is the whole package so people wouldn't get much out of parts.  I could
put it online for you, formatted, but honestly I don't want to do that
until I have read it and see if I think its worth a sh.t.  (Really, I
do think its probably very good information, I just don't know and
don't want to commit until I do.)

Regards,

laurel

> Hi Paul
>
[quoted text clipped - 30 lines]
> >Please post your information and lifestyle here for the benefit of all
> >who read this list. ......
I.P. Freely - 22 Mar 2006 04:58 GMT
> Tom,
>
[quoted text clipped - 10 lines]
> You could also post a summary, too, but it sounds like the information
> is the whole package so people wouldn't get much out of parts.  

Good advice; I should follow it more often myself when my posts get too
long. When I recognize that, and think to do it, I'll add a one-sentence
short version at the top -- and label it as such -- so readers can
choose up front whether the journey to that conclusion interests them.

Example lead-in for this case: "I chose WW due to (e.g. religious
reasons, fear, heart problems, cost) [convinces us you've thought this
through], researched it to Hellenbach [supports your claims that chicken
lips may promote apoptosis], and came up with this WW plan [oh, it's a
PLAN, rather than just ramblings]. It's long [thanks for the warning],
but much of it would be of use to those who want to supplement their
RP/RT/ADT/whatever with anything else that could help and will do no
harm [now ANYBODY should see the value in that]."

I.P.
Thomas Gentles - 22 Mar 2006 22:15 GMT
Hi Paul, Laurel and I.P.

I'm grateful for your suggestions. Particularly Laurel's offer to
read and post the article it if it's worth a ****.

But I've thought about this for quite a bit these last few days.
And for now I think I'll just reiterate my offer to send that
report and graph personally to anyone interested.

All anyone interested has to do is just send me a personal e-mail.
One or two words is all I need and I'll be glad to send it.

The reason I do this is to avoid cluttering the postings if only a
few people are interested. And I feel that if it's to be posted
I'd still have to do quite a bit of editing. When maybe it's the
substance that needs to be reviewed.

I'd be interested in anyone's comments. Privately or publically
And if there's any encouragement I might accept Laurel's offer
later if it's still there.

Thanks very much again for the advice you've given me.

Tom

>Tom,
>
[quoted text clipped - 53 lines]
>> >Please post your information and lifestyle here for the benefit of all
>> >who read this list. ......
N268ME@gmail.com - 20 Mar 2006 00:08 GMT
> I've been doing lots of on line research, but there seems to be a
> paucity of current information on long-term studies relating to success,
> or failure, of the various treatment methods--or perhaps I'm just
> missing them.

You're not missing them, they don't exist.  One of the most difficult
parts of the decision making process is to understand that really long
term data regarding the efficacy of one treatment over another just
isn't out there.  The studies are underway, but with a slow growing
cancer such as PCa usually is, any treatment option or no treatment
usually results in similar 5 and 10 year survival rates, the benchmark
that other cancer treatments are judged by.
I agree with the others, get educated and pick what works best for you,
chances are, you will not make a bad decision whatever you pick.
FWIW, I chose surgery.  I was diagnosed at 46.
Good luck.
CPW
Naaman - 29 Mar 2006 19:59 GMT
Just got results of latest PSA 3/27: 4.0.

I'm scheduled to meet with my urologist in about 10 days to discuss this
latest result and see what, if anything, he suggests we do next. I will
probably set up an appointment with a radiation oncologist that has been
recommended just to further educate myself. Also probably will quiz my
urologist more about RP.

Meanwhile, I'll continue to monitor this newsgroup (which is a wonderful
support group), do my homework and think positively.

Naaman

> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 20 lines]
>
> Naaman Nickell
I.P. Freely - 29 Mar 2006 22:57 GMT
> Just got results of latest PSA 3/27: 4.0.
>
[quoted text clipped - 6 lines]
> Meanwhile, I'll continue to monitor this newsgroup (which is a wonderful
> support group), do my homework and think positively.

Good start, Naaman. Does that homework include studying pertinent
chapters of 2 or 3 PC books? You may as well begin now, because you'll
need the info sooner or later even if it's not time to act yet. I've got
several, and each time my situation -- numbers, treatment phase, etc. -
changes I'll read another chapter or two. We want our knowledge to keep
up with, maybe stay slightly ahead of, our situation so we recognize
when it's time to get involved again and can ask good questions.

I.P.
Naaman - 30 Mar 2006 00:21 GMT
>> Just got results of latest PSA 3/27: 4.0.
>>
[quoted text clipped - 16 lines]
>
> I.P.

I have a library copy of Strum's book and have it and Scardino's book on
order from Amazon. Also, I have a copy of Report to the Nation on
Prostate Cancer from the Prostate Cancer Foundation. From time to time,
I visit the message boards at the American Cancer Society web site.

Naaman
Naaman - 12 Apr 2006 01:48 GMT
> Two months ago, my urologist called to tell  me that my prostate biopsy
> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 20 lines]
>
> Naaman Nickell

Just returned from a visit my urologist He says the fact that my PSA now
is down to 4.0 is good, and that he wants to wait four months and check
it again. He also did a DRE and found that the area of the prostate in
which the biopsy showed cancer is smooth on the surface. Of course, the
cancer is still there inside.

Meanwhile, I plan to schedule an appointment with another urologist for
a second opinion and an appointment with a radiation oncologist to talk
about brachytherapy.

I also made contact with a support group in Tucson and will attend their
next meeting, where I hope to learn more about the local experiences of
others with respect to doctors, hospitals and treatments.

Naaman
juniper - 12 Apr 2006 05:28 GMT
> Just returned from a visit my urologist He says the fact that my PSA now
> is down to 4.0 is good, and that he wants to wait four months and check
> it again. He also did a DRE and found that the area of the prostate in
> which the biopsy showed cancer is smooth on the surface. Of course, the
> cancer is still there inside.

This is all very good, Naaman, and I am happy for you.  Because of my
personal experience, I don't believe too strongly in the biopsy
results.  Our biopsy was very very far off.  It showed <5% cancer total
in all the cores, and only 2 of 10, and a gleason of 3+4(7).  We really
had pervasive cancer and a gleason of 9.  But you can mostly ignore my
experience, because our PSA was 24, more or less.  Still, I am sure
someone will tell you to have your biopsy read by a specialized lab,
and I think that is important even though it didn't help me.  Also,
what is your complete Gleason score?  A Gleason is made up of two
numbers.  Yours equals 6, but that could be 2+4 or 3+3 or 4+2 or 1+5--
you get the idea.  It is those numbers, and which comes first, that
really tell you something.  The total score by itself, for a 6, is not
very helpful.

> Meanwhile, I plan to schedule an appointment with another urologist for
> a second opinion and an appointment with a radiation oncologist to talk
> about brachytherapy.

This is an excellent plan.  You would do well to get all your records
from your doctor and the labs (including biopsy pathology) to put in a
folder and take with you to the other appointments.  I know your doctor
is professional so I am sure he will not mind.  If he did mind, it
wouldn't matter, because it is your right to get your records.  At any
rate, you will learn far more from your other consults if they can see
everything to date.  Then they won't have to be playing catch up, and
will be able to give you the most information as well as let you know
if you need additional information.

> I also made contact with a support group in Tucson and will attend their
> next meeting, where I hope to learn more about the local experiences of
> others with respect to doctors, hospitals and treatments.

I don't care what anyone says, shared personal experience is an
excellent learnign tool.  How many times have we all shook our head
over hard-won experience (painful, or expensive, or whatever) that we
could have been saved had we had the benefit of someone who was there
first?

I am happy to see that you (a) got good news and (b) are making very
plans to follow through.

regards,

laurel
Naaman - 12 Apr 2006 06:08 GMT
>> Just returned from a visit my urologist He says the fact that my PSA now
>> is down to 4.0 is good, and that he wants to wait four months and check
[quoted text clipped - 15 lines]
> really tell you something.  The total score by itself, for a 6, is not
> very helpful.

My Gleason was 3+3. Should have realized sooner I had left it out.
Thanks for calling it to my attention.

BTW, my biopsy was read by Dianon Systems.

>> Meanwhile, I plan to schedule an appointment with another urologist for
>> a second opinion and an appointment with a radiation oncologist to talk
[quoted text clipped - 9 lines]
> will be able to give you the most information as well as let you know
> if you need additional information.

I'll keep this advice in mind as I proceed. Help from those who have
been there before is a wonderful gift.

>> I also made contact with a support group in Tucson and will attend their
>> next meeting, where I hope to learn more about the local experiences of
[quoted text clipped - 12 lines]
>
> laurel

Naaman
David Mueller - 14 Apr 2006 16:45 GMT
At your age you might be a candidate for "watchful waiting".  If that's not
an acceptable option for you, with your numbers I'd surely consider
radiation. The surgery is truly "radical", difficult to do, and requires
that you find rare talent. One good source of information I found was Don
Cooley's site at http://www.prostate-help.org/.
>> Two months ago, my urologist called to tell  me that my prostate biopsy
>> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 36 lines]
>
> Naaman
Naaman - 14 Apr 2006 19:59 GMT
It seems as though WW is what my uro and I are doing for the next four
months, at least. He told me not to get in a rush to do anything at
present. I assured him I wouldn't.

I will check out the web site you suggested. This ng has been the source
of invaluable information for me, although at times I worry about
information overload. However, I suspect as I continue along this road I
shall be seeking more and more advice from those who make ascp a "must"
place for me to visit

Naaman

> At your age you might be a candidate for "watchful waiting".  If that's not
> an acceptable option for you, with your numbers I'd surely consider
[quoted text clipped - 40 lines]
>>
>> Naaman
juniper - 14 Apr 2006 20:26 GMT
> of invaluable information for me, although at times I worry about
> information overload. However, I suspect as I continue along this road I

This has been a very real problem for me two or three times.  It seems
like you swim in the information and it is useless, there is so much
and you can't remember it all and it is contradictory and so on.  Then
it all falls into place (eventually; it does not feel like that will
ever happen) and suddenly you are educated in PCa.  At that point it
becomes useful.  I have gone through this process for: initial
diagnosis, ADT, and for salvage RT.

Also, Steve and I learn it very differently.  I kind of swim in it,
reading, writing, arguing.  He reads carefully, making notes, looking
up terms.  Very step-by-step.  It seems like we both go through the
same stages to the same end, even though the process is different.

I am writing to encourage you that all this time is not wasted, and the
overload is not permanent.  You are fortunate you had good initial
doctors (your GP & uro), and wise to take the steps you are planning.
I am confident that your end result will be the best possible.
dale.j. - 15 Apr 2006 00:42 GMT

> >> Two months ago, my urologist called to tell  me that my prostate biopsy
> >> had revealed a tiny bit of cancer and  that he wanted to talk face to
[quoted text clipped - 36 lines]
> >
> > Naaman

Perhaps radiation would be a possible choice.  You should at least check
it out and get a second opinion from a radiation doctor.

Signature

Email:  dalej2@mac.com

Naaman - 15 Apr 2006 02:14 GMT
>  
>>>> Two months ago, my urologist called to tell  me that my prostate biopsy
[quoted text clipped - 39 lines]
> Perhaps radiation would be a possible choice.  You should at least check
> it out and get a second opinion from a radiation doctor.

Thanks for the suggestion, Dale. I am in the process of setting up an
appointment with a radiation oncologist in Tucson to discuss my options
in that area, although at the moment I am most interested in seed
implants. Lots of questions still to ask.

Naaman
 
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