Home | Contact Us | FAQ | Search & Site Map | Link to Us
Sign In | Join | Other 45 Sites in Network
Home
Discussion Groups
General
GeneralCardiologyVisionDentistryPharmacyLaboratoryNutritionAlternative
Diseases and Disorders
AIDSAlzheimer'sArthritisAsthmaCancerBreast CancerDiabetesEpilepsyGlaucomaHepatitisHerpesLupusProstate BPHProstate CancerProstatitisSinusitisTinnitus

Medical Forum / Diseases and Disorders / Prostate Cancer / September 2007

Tip: Looking for answers? Try searching our database.

When (if ever) can we consider ourselves cured

Thread view: 
Enable EMail Alerts  Start New Thread
Thread rating: 
David&Joan - 26 Aug 2007 23:16 GMT
Well, I stirred up a bit of controversy over my statement that I considered
myself "cured" after 14 months of straight PSA zeros following surgery.

Perhaps we all have our own definitions of "cured". I believe that I have
less chance now of recurring PCa than a 60 year old (my age) developing PCa
who has not yet been diagnosed with PCa and has a PSA of <4. I know that
isn't really cured. It just makes me feel better to think that way.

But seriously now. What are my chances of recurrence? I started with a PSA
of 5, Gleason 6 (later raised to 7 after surgery), type T1c, bi lateral
invovlement, negative margins and negative lymph node involvment. Isn't it
somewhere in the 5% range?

And what are the mechanisms of recurrence. I presume that PCa cells escape
from the gland through the blood stream and lymphatic system, ie
metasticiscm (is that a word?). Metastatic PCa cells are trapped and
destroyed by our immune system. It is only those little critters that get by
our immune system and settle somewhere and multiply. Do I have this right?

Given that I had a tiny amount of PCa cells to start with and they all
stayed within the gland (at least the gross masses that can be detected by
pathology) then I would think that the metastatic types are slim and
hopefully now none. What do you guys think?

David

David
ronju99 - 26 Aug 2007 23:45 GMT
Probably the only way we'll be considered cured is when we die of something
other than prostate cancer.  It's never 100%. But if calling oneself cured
makes one sleep better at night then call it and sleep tight.

Ron S.
ronju99 - 27 Aug 2007 12:08 GMT
I obviously respectfully disagree with the mainstream definition of cure.
Cure means you have no prostate cancer cells in your body. Setting
artificial time periods for a definition is only done for two reasons. One
to help reduce the stress of not knowing and the other to promote a
treatment option.

Bottom line; There is no Cure for prostate cancer.
Anyone that tells you otherwise is blowing smoke somewhere.

All anyone has after being diagnosed with prostate cancer are choices of
treatment that will keep the cancer at bay hopefully until he dies of
something else.

Ron S.
djperry42@sbcglobal.net - 27 Aug 2007 16:44 GMT
The only people cured of cancer are those who died of something else
before a recurrence of the cancer.  As mentioned by others, people get
recurrences five, ten and more years out.  Stats I've seen indicate
that 30% of all men treated for prostate cancer will get a recurrence,
and of those 70% will get a return in the first three years, 25% the
next two years, and 5% after that.  These figures of course are for
all stages and pathological outcomes.  An individual with a Gleason 6,
no positive margins, etc., has better percentages than someone with
less favorable numbers.

By the way, something someone somewhere might need to know some day, I
was at a barbeque on Saturday where there were some doctors and
somehow a discussion of sex-change surgery came up.  It turns out when
a male is surgically altered to female status, the prostate is left
intact so DRE's continue to be part of the physical exam although it
is done both rectally and vaginally offering a more complete exam than
the anal approach alone can provide.  Just another one of those "gee
whiz" things you might want to know.
Dave Perry
Just - 26 Aug 2007 23:58 GMT
snip........

>Given that I had a tiny amount of PCa cells to start with and they all
>stayed within the gland (at least the gross masses that can be detected by
>pathology) then I would think that the metastatic types are slim and
>hopefully now none. What do you guys think?
>
>David

Hi David!

I had salvage RT some two years ago - six years after RP.

At that time I met another guy having salvage RT that had RP fifteen
years prior (yes, 15 years...). Probably this guy had considered
himself cured. Luckily for him, he carried on having regular PSA
tests...

Just
Steve Kramer - 27 Aug 2007 00:08 GMT
> What do you guys think?

2 years without cancer    99%
5 years without cancer    98%
7 years without cancer    97%

This is from the Slone-Kettering nomogram, based on what I think you have
told us.  But..

7. What should I do with the results produced by the nomogram?

These nomograms cannot definitively answer the question of which treatment
is most appropriate for an individual patient. These tools simply provide
information useful for the decision-making process, which should be carried
out in consultation with a physician.
Steve Jordan - 27 Aug 2007 00:17 GMT
On August 26, David wrote:

> Perhaps we all have our own definitions of "cured". I believe that I have
> less chance now of recurring PCa than a 60 year old (my age) developing PCa
> who has not yet been diagnosed with PCa and has a PSA of <4. I know that
> isn't really cured. It just makes me feel better to think that way.

Endless chewing over of the numbers will not change the fact that no one
considers a case of PCa "cured" until the passage of at least five years
from primary treatment (tx) with no recurrence. "Recurrence" is defined
differently by various entities. The ASCO (American Society of Clinical
Oncology) defines it as three consecutive rises in PSA. Also called
biological or clinical failure.

> But seriously now. What are my chances of recurrence? I started with a PSA
> of 5, Gleason 6 (later raised to 7 after surgery), type T1c, bi lateral
> invovlement, negative margins and negative lymph node involvment. Isn't it
> somewhere in the 5% range?

The uro, no matter what he claims, simply does not have any means of
being *certain* that PCa cells have not found homes elsewhere, likely
the lymph nodes, possibly bones. But maybe not. No one can tell.

> And what are the mechanisms of recurrence. I presume that PCa cells escape
> from the gland through the blood stream and lymphatic system, ie
> metasticiscm (is that a word?). Metastatic PCa cells are trapped and
> destroyed by our immune system. It is only those little critters that get by
> our immune system and settle somewhere and multiply. Do I have this right?

Close enough, I think.

> Given that I had a tiny amount of PCa cells to start with and they all
> stayed within the gland (at least the gross masses that can be detected by
> pathology) then I would think that the metastatic types are slim and
> hopefully now none. What do you guys think?

This guy thinks that, to paraphrase a piece of wisdom, eternal vigilance
is the price of optimum outcome. Keep testing.

It appears that there is a fairly good chance that there will not be any
recurrence. But I would not bet my life on it and kick back and forego
periodic tests to determine what's going on....

Caveat: Everyone is different.

Regards,

Steve J

"As a physician, I am painfully aware that most of the decisions we make
with
regard to prostate cancer are made with inadequate data."
-- Charles L. "Snuffy" Myers, MD
Medical oncologist. PCa survivor.
ron - 27 Aug 2007 00:22 GMT
Hi David...I've responded within your original text...Best wishes and
good health, ron

On Aug 26, 4:17 pm, "David&Joan" <djmarch...@cox.net> wrote...snip...
> But seriously now. What are my chances of recurrence? I started with a PSA
> of 5, Gleason 6 (later raised to 7 after surgery), type T1c, bi lateral
> invovlement, negative margins and negative lymph node involvment. Isn't it
> somewhere in the 5% range?

More questions, were you a 3+4 or 4+3?  And, how many years down the
road are you asking about?

You can use the Hopkins' nomograms which give you a snapshot of how
Walsh's patients faired over time, your surgeon may do better or
worse.  I provided a hard and a web reference in the earlier thread.
If one of Walsh's men were a pathological 3+4 with organ-confined
disease and a pre-op PSA in the 4-10 range, then at 10 years post-
treatment he'd have about an 11% chance of biochemical recurrence, on
average.  If he were a 4+3, the number would increase to around 23%,
again at 10 years.  To a first approximation, recurrence rates are
roughly linear with time (actually, I suspect this is a worst case
assumption, because there does appear to be some flattening in the
curves for higher-risk men, that I'd like to believe is also there for
lower-risk men).  So, at 5-years cut the numbers in half; at twenty
years, double them.  Also, these numbers were projections for men
treated in 1999.  Walsh and others have found that men have better
results the later the year of surgery ("year of RP factor").  This is
probably due to a multitude of factors, some real, like improved
surgical methodologies, and some artificial, like Gleason grade
inflation.

> And what are the mechanisms of recurrence. I presume that PCa cells escape
> from the gland through the blood stream and lymphatic system, ie
> metasticiscm (is that a word?). Metastatic PCa cells are trapped and
> destroyed by our immune system. It is only those little critters that get by
> our immune system and settle somewhere and multiply. Do I have this right?

PCa tumor cells can be detected in the blood system prior to
treatment, their concentration seems to generally parallel the
aggresiveness of the disease.  If none of them survived, and if the
prostate was effectively removed or ablated such that no cancer cells
remained in prostatic tissue, and no healthy prostate tissue remained
for the genetic error to be repeated, then, I think, you would be
cured.  Even if these conditions are not met, you may be "effectively"
cured.  That is, you may die from something else before detectable
concentrations of tumor cells reappear.

> Given that I had a tiny amount of PCa cells to start with and they all
> stayed within the gland (at least the gross masses that can be detected by
> pathology) then I would think that the metastatic types are slim and
> hopefully now none. What do you guys think?

The numbers above give some idea of the odds.  To borrow and slightly
alter an old phrase, "Hope for the best, but verify."

> David
>
> David
Bob Anthony - 27 Aug 2007 21:57 GMT
David:

The one thing that is certain, this a very frustrating and confounding
disease. Even experts disagree on the treatment choices available and
just when and how to implement them.
Firstly, there are the many treatment options which is strictly an
individual choice, of course depending upon the educated guess work of
the Partin Tables and the small amount of biopsy samples taken.
Secondly, there the side effects from each specific treatment which can
be different for each individual.
Thirdly, there is the constant blood testing to see if the treatment has
indeed worked with the never ending 3 or 6 month psa tests. It kind of
reminds me of a prisoner going to the parole board.
Fourthly, if all that were not enough, there are the uncertainties of
being really cured 2, 5, 10, 15 years out! Please! It took x amount of
time for the PCa to be detected in the first place, and it stands to
reason that everyone is a test away from some kind of medical problem of
one kind or another PCa or not.
Fifthly, no one really knows how we really got the damn thing in the
first place and how to have prevented it from even happening! Of course,
not to mention the sexual frustration that can go hand in hand with PCa
and treatments and the psychological toll it takes on us in our
otherwise healthy bodies.
This tells me is that the current slash/burn methods for cancer are
really not excellent definitive cures at all, be it PCa or for any
cancer for that matter.
Until medical science delves much much deeper, until medical science
really understands the root of cancer; the prevention, as well as the
definitive cure will continue to be uncertain at best to us all. I feel
that medical science is only on the cusp of knowing what can ultimately
happen to us regarding the final outcome of such a complex disease as
PCa whatever the pathology may be. Again, some on this newsgroup have a
better knowledge of their final outcomes due to their advanced cases.
Even then, there may be cures for them too only years away.
I remember about 5 or 6 years ago when a friend of mine had to go for a
triple bypass surgery and a mitro valve repair. I assured him then that
everything would go well because it is was a pretty cut and dry
procedure, even if it is considered very a major surgery. After all, "it
was not cancer" I had told him. Only now do I really feel what I had
meant when I uttered those words, "It's was not cancer".

B.A.
chasjac too - 28 Aug 2007 01:52 GMT
Hello:

I've been staying away from the term "cured" in all my dealings with friends
who ask about it.  When I must refer to my status, I simply say that I am a
cancer survivor.  I will probably never know if it's gone.  But I am alive,
so it has not gotten me so far.  

--charlie

Signature

6/2006 PSA 5.2, DRE suspicious
7/2006 Biopsy:  2 of 10 positive, Gleason 7(3+4)
11/2006 LRP:  Clear margins
PSA < 0.01 on 1/2007, 3/2007, 6/2007
so far, so good ...

I.P. Freely - 28 Aug 2007 17:59 GMT
> Hello:
>
> I've been staying away from the term "cured" in all my dealings with friends
> who ask about it.  When I must refer to my status, I simply say that I am a
> cancer survivor.  I will probably never know if it's gone.

What he said.

When they ask if it's in remission, or cured, or more cautiously how I'm
doing, I  say -- because it's the most honest and likely assessment --
that I had the source cut out, it will probably return to bite me some
day, but until then it's usually less bothersome than, say,
telemarketers or tailgaters. You might call it "hypothetical cancer" at
this point.

As I was walking past a lady who knows I had PC, I overheard her make a
joke to someone about her "performance anxiety" in some unnamed arena. I
told her the cure for that was to have her prostate removed. She didn't
have to press for details to get the implications and the  joke. I don't
think of myself as a "cancer survivor" any more than a shoulder
reconstruction survivor or a hernia repair survivor or a broken rib
survivor; each laid me up for a few weeks, after which life resumed. My
*pads* are real, but my PC is just hypothetical for now.

Those of us who have not yet encountered treatment failure mustn't let
our now-hypothetical cancer obscure the many other, often more
manageable, maladies that arise at our age. What I'm more immediately
concerned about and paying more attention to now is my rising blood
glucose, aka prediabetes. I think that's statistically and practically a
bigger but more manageable threat than my hypothetical PC over the next
decade or so, so it deserves more attention.

I.P.
kh - 30 Aug 2007 01:03 GMT
> Given that I had a tiny amount of PCa cells to start with and they all
> stayed within the gland (at least the gross masses that can be detected by
> pathology) then I would think that the metastatic types are slim and
> hopefully now none. What do you guys think?

I think you're worried about the wrong thing.

I'm 3 years out from IMRT/pd seeds/8 months Lupron.  I recurred to
beat the band, went from PSA 1 to 60 in about a year.  This thing
almost killed me.

I'm back on Lupron and did 3 months of Casodex.  It seems under
control.  My PSA dropped like a rock. I'll get some blood pulled for a
PSA reading tomorrow.

I know I gotta watch this and the docs say that I'll be on Lupron
forever.

As bad as this is, consider that I know two guys who went into cardiac
arrest in their 40's.  Fortunately both survived.

Stuff happens.  We gotta deal with it.

Thus far, I have the following Lupron issues.  Intermittent sharp pain
in small joints.  Hot flashes, 3 or 4 times a day.  Some sleep
disorders.

On the other hand, I can still raise the flag. It's not easy and it
doesn't go all the way up the pole but it's better than nothing.

My fasting blood sugar is in the 100-110 range on two 850 glucophage/
day.

My weight is down 20 pounds from the peak last year.

I can run up 3 or 4 flights of stairs, then walk a half mile to cool
down.

If your PSA is under 1, just track it.  If it rises, see a medical
oncologist.   I think the focus should be your quality of life.

Diabetes, heart disease, stroke, other ailments are a bigger issue.
I don't like being on Lupron but so far, it's worked well.  I'm not
counting on it but I'm hoping for that silver bullet.  It might be
Provenge.  It might not.

-kh
Leonard Evens - 03 Sep 2007 16:31 GMT
> Well, I stirred up a bit of controversy over my statement that I considered
> myself "cured" after 14 months of straight PSA zeros following surgery.
[quoted text clipped - 8 lines]
> invovlement, negative margins and negative lymph node involvment. Isn't it
> somewhere in the 5% range?

I think my case may be similar to yours, and I've tried to make
estimates of recurrence sometime during my lifetime.  I believe that the
probability of recurrence in any given year is pretty small, so it would
be irrational to worry about it. My cancer was diagnosed and treated
when I was 67, and I am now 74.   There hasn't been a recurrence, and
while that might happen, it is much more likely that I will die of some
other disease, and that even if I do have a recurrence, it will have a
relatively minor effect on my life span and quality of life.

To see why it is difficult to make estimates of this kind consider the
following model of what might be happening in cases like ours.  The only
data we really have show the number of men without recurrence at any
given year after treatment for ten years or longer.   The data is noisy
enough in low risk cases so that it is not possible to determine the
shape of that curve, particularly for later years.   It  could be just
linear or it could tend to flatten out.   If it were linear, the risk in
any given year would actually be going up slightly with time, and if it
flattens out, the risk could be constant or could be decreasing over
time.   Now to make estimates you have to invent a mathematical model of
what is going on.  Presumably some men are cured completely and have no
trace of prostate cancer in their bodies.  For such men, recurrence is
impossible.   Other men may still have traces of prostate cancer which
the body keeps under control.  Such men may have a recurrence, but in
cases like ours, that risk may still remain small in in any given year.
 Unless you know just how the cases break up,  you can't really
construct a plausible model to use to make estimates.  The best you can
come up with is aworst case analysis, but that could be very far off.

My calculations show that in my case  T1C, PSA 4.5, Gleason 7=3+4, the
likelihood of recurrence within 25 years after my surgery is perhaps as
high as 23 percent, but probably it is significantly less than that.
Also, the model I am using may be entirely wrong.  I am now 74, and I
doubt very much that I will make it to 99, so it would be foolish of me
to worry about recurrence given what I know.  That doesn't mean that I
don't get up tight each year when I have my PSA tested, but that is the
only time I am bothered by such fears.

> And what are the mechanisms of recurrence. I presume that PCa cells escape
> from the gland through the blood stream and lymphatic system, ie
> metasticiscm (is that a word?). Metastatic PCa cells are trapped and
> destroyed by our immune system. It is only those little critters that get by
> our immune system and settle somewhere and multiply. Do I have this right?

Remember that what is happening at the level of cells may be very
complex.   A naive model which might make sense to your or me may be far
wide of the mark.  Also, even an expert doing research in the filed may
not know enough to say just what is going on.  Think of the parable of
the blind men and the elephant.

> Given that I had a tiny amount of PCa cells to start with and they all
> stayed within the gland (at least the gross masses that can be detected by
> pathology) then I would think that the metastatic types are slim and
> hopefully now none. What do you guys think?

As I said, it is quite possible that you now have no cancer cells in
your body at all.  But this is something that no one may ever be certain
about.  Even if a thorough autopsy is done after you die, it might not
be able to find cancer cells that are still present.  On the other hand,
some researcher might develop a test which can show the presence of a
small number of cancer cells tomorrow.  It is pointless, I think, to
conjecture about such things.

> David
>
> David

Good luck.
I.P. Freely - 03 Sep 2007 18:47 GMT
> It is pointless, I think, to
> conjecture about such things.

And that, IMO, is very important. I've done all I'm willing to do to
"cure" any hypothetical remaining PC, because the next step would
significantly degrade my QOL with very little -- and only hypothetical
-- benefit. (History: PSA 8.8 but rising rapidly pre-RRP, Gleason 8,
negative RRP margins, zero PSA for almost three years now, age 64 now,
but recurrence is probably still a coin toss because of the G-8 and
seminal vesicle involvement).

If my PSA starts rising again -- it's gonna do whatever it's gonna do --
  I'll hit the books again and research my next step once a next step
is justified by facts rather than fear. In the meantime any remaining PC
in my body is on its own, as I have many more rewarding and/or
productive pursuits to carry on.

Or maybe I should read the Walsh thread before hitting SEND.

Nahh ... If that changes my mind, I can always change my mind and plan.
PC gives us that kind of time.

I.P.
 
Sign In
Join
My Latest Posts
My Monitored Threads
My Blog
My Photo Gallery
My Profile
My Homepage

Start New Thread
Enable EMail Alerts
Rate this Thread



©2008 Advenet LLC   Privacy Policy - Terms of Use
This website includes both content owned or controlled by Advenet as well as content owned or controlled by third parties.