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Medical Forum / Diseases and Disorders / Prostate Cancer / January 2005

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Hormone Therapy Post Radiation

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Maurice - 16 Jan 2005 17:59 GMT
Diagnosed 01/03 Gleason T2B/T2C 4:3, PSA =13,  Age 69. Hormones started
02/03 (Lupron & Casadex).
Radiation 04/03 thru 05/03 (39).
PSA since Radiation  = .018.
Doctor suggests hormones forever.  Have "hot flashes"  several times per day
and night.
Need to see Dr. 02/05 and decide if I will continue.

Any suggestions?  Maurice (oatesm@visuallink.com)
I.P. Freely - 16 Jan 2005 18:26 GMT
How much have you read about it, here and in the many books and GOOD web
sites? How well are you tolerating the hot flashes? Other SEs? How's your
bone density? Willing to risk permanent SEs and increased (HT-INDUCED!) risk
of higher-grade recurence (at two years on HT there's already risk of
those)? How's your QOL now? Your PSA DT is apparently infinite (OK, well >
24 months, thus quite encouraging), so what's the doc's motivation for
inducing SEs for the rest of your life? Are you on meds to suppress the
flashes? To protect your bones?

I.P.

"Maurice" <oatesm@visuallink.com> wrote >
> Any suggestions?
gourd_dancer - 16 Jan 2005 19:04 GMT
Maurice, ask for Eligard in lieu of Lupron. Eligard is relatively new and
very few people have hot flashes as a side effect.

First shot of Lupron (3mo) caused 5-6 hot flashes and nightly night sweats a
day. I have been on Eligard (3 mo) for 7 months and have yet to have a hot
flash. I average 2 night sweats a week.

Best of luck,

Mike

> Diagnosed 01/03 Gleason T2B/T2C 4:3, PSA =13,  Age 69. Hormones started
> 02/03 (Lupron & Casadex).
[quoted text clipped - 5 lines]
>
> Any suggestions?  Maurice (oatesm@visuallink.com)
Steve Kramer - 17 Jan 2005 15:09 GMT
First, lemme welcome you to our club knowing that it was not your intent to
do so.  Second, lemme assert that since your doc has already spoken, I feel
uncomfortable providing a counter opinion.

Assuming your Gleason is 4+3=7 and your Stage is T2c, you are at the
borderline for decisions leaning away from surgery and towards radiation
and/or homone treatment.  However, once accomplished, I do not see anything
that would keep you on hormones.  At least not until you've determined there
is still something growing in you.

Unless your doc has evidence that cancer cells survived the radiation, I
would have him back off on the hormones and get quarterly PSA tests for a
couple of years.

Signature

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

> Diagnosed 01/03 Gleason T2B/T2C 4:3, PSA =13,  Age 69. Hormones started
> 02/03 (Lupron & Casadex).
[quoted text clipped - 5 lines]
>
> Any suggestions?  Maurice (oatesm@visuallink.com)
Alan Meyer - 17 Jan 2005 15:29 GMT
> Diagnosed 01/03 Gleason T2B/T2C 4:3, PSA =13,  Age 69. Hormones started
> 02/03 (Lupron & Casadex).
[quoted text clipped - 5 lines]
>
> Any suggestions?  Maurice (oatesm@visuallink.com)

I'm not a doctor and don't want to play one on the Internet, but I
personally have doubts about a hormones forever strategy.  Here's
why:

First, you may not need it.  It is possible that the therapy you had
has already defeated the cancer.  You have no way of knowing that
one way or the other because you've never seen what your PSA is
in the absence of Lupron.  If you take no more Lupron, then wait
to see what your PSA does, you may find that it stays relatively low
even without the Lupron.  With the Lupron gone it may well go up
some, but my radiation oncologist told me that as long as it stays
below 1.0, then there's nothing to worry about.

Second, even if the cancer is not under control, you may actually
benefit more from intermittent hormone therapy than from
continuous HT.  The idea is to wait until the PSA reaches some
threshold (don't know what that should be and I don't know if there
is any scientific consensus on it), then knock it back with HT, then
wait again for it to reach the threshold.  Some doctors believe that
intermittent HT provides longer survival as well as fewer side
effects as compared to continuous HT.

Hormones _do_ have side effects and hot flashes are not
necessarily the worst of them.  Bone weakening and osteoporosis
are possibilities.  Joint pain is a possibility.  Loss of libido is a
certainty.  Muscular weakness and tiredness are possibilities.
Some doctors seem to take the view that hormone therapy is
no big deal and it provides protection against growth of the disease.
But the side effects are real and the protection is limited.

   Alan
Olfart - 17 Jan 2005 15:40 GMT
> > Diagnosed 01/03 Gleason T2B/T2C 4:3, PSA =13,  Age 69. Hormones started
> > 02/03 (Lupron & Casadex).
[quoted text clipped - 37 lines]
>
>     Alan

I agree with Allen and Steve 100%. Went "intermittant last week. In addition
to their comments let me add that there is no such thing as "Hormones
Forever". At some point in time - 2 or three years is a good guestimate you
will become Hormone Refractive which means the cancer cells, if any still
exist, will no longer be starved by the lack of testosterone and will
comence growing again. Intermittant hormone therapy may should give a longer
time to use the therapy before is becomes useless.  Monitoring PSA and
Testosterone levels will tell your Uro if and when to restart hormone
therapy - could be you may never need to resume it.
Talk to your Doc and get a second opinion if he refuses to consider
intermittant. A Medical Oncologist would be a good choice. And good luck on
your decision - keep us posted. We are not doctors-but we are in the same
shoes as yours - and we care.
George
Age - 69
8/12/02 - PSA 3.7
10/13/03 - PSA 4.69
11/11/03 - PSA 4.8
11/18/03 - Biopsy - 10 cores
one core-25% of core-Gleason 4+4=8
all other cores benign tissue
12/10/03 - Consult - Oncologist MD
12/16/03 - Consult - Radiation Oncologist
Treatment Plan - Northeast Ga Cancer Center
HT - started 12/17/03 - Eulixen & Lupron (2nd 4 mo Lupron-4/26)
2/10/04 - Started - Flowmax and Megastrol
Radiation - IMRT to begin 3/30/04 - 42 treatments - Completed 6/8/04
No seeds due to Prostate problems
8/30/04 - 1 yr Viadur Implant instead of 4mo Lupron
12/14/05 - Removed implant - trying intermittant HT for a while.
I.P. Freely - 17 Jan 2005 17:19 GMT
My university team of oncologists (a whole interdisciplinary tumor board
that discusses me weekly) want me on HT post-RP for at least two years
despite PSA = .006 (it was 8.8 pre-RP) just because I was Gleason 7 and 8
and was T3cN0M0 with negative margins . . . just in case one of those
Gleason 8 cells is lurking out there.

That's the conservative side of the adjuvant therapy coin, aiming at a
complete cure while any micromets are at their most vulnerable.

I.P.
Alan Meyer - 18 Jan 2005 03:05 GMT
> My university team of oncologists (a whole interdisciplinary tumor board
> that discusses me weekly) want me on HT post-RP for at least two years
[quoted text clipped - 6 lines]
>
> I.P.

I wish the doctors knew more about all this but, unfortunately,
precise knowledge about the value of HT, how it should be used,
and for how long, does not seem to yet be available.

When I was planning radiation treatment for my Gleason 4+3
cancer at the National Cancer Institute (not a shabby organization),
I asked my doctor about getting neoadjuvant HT.  Another
oncologist had recommended it to me.  She said I could have it
if I wanted it, but she recommended against it on the grounds that
the long term effects of HT are not known.

I opted to get HT, but discontinued it after 4 months of treatment,
in part because I didn't like it, in part because I thought from some
reading I had done that the main benefit would be had before and
during RT rather than after, and in part because it appeared to have
caused dangerously elevated liver enzymes in my system.

I'm still waiting to see some definitive studies that everyone agrees
on that tell us what to do.  In the meantime, like so much in PCa
treatment, it seems that we have to make personal choices as best
we can.

   Alan
 
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