Medical Forum / Diseases and Disorders / Prostate Cancer / September 2007
When (if ever) can we consider ourselves cured
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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.
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