Medical Forum / Diseases and Disorders / Prostate Cancer / November 2004
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TINKPOTDUDE II - 31 Oct 2004 18:48 GMT I have been diagnosed with very little prostate cancer. Out of 14 snippets taken during my biopsy, only one showed a trace of just 5%.
I refuse to have the prostatectomy! However, I have heard wonderful things about the freezing procedure.
Will some of you be good enough to let me hear from you via email about this method? I understand it only kills the cancer cells.
Thank you for your help in this matter.
Edward
Danny McCarty - 31 Oct 2004 19:04 GMT >Subject: QUESTION >From: MRROTHROCK@webtv.net (TINKPOTDUDE II) [quoted text clipped - 13 lines] > >Edward You left out the other important item- what was the Gleason score. Persons with serious prostate cancer widespread in the prostate frequently have a totally negative biopsy. Your single core with "only" 5% does NOT mean that the cancer is minor. Regardless of the method of doing it, the entire prostate MUST be removed or killed. The choice of method- RRP, radiation, cryo, whatever, is based on efficacy and aftereffects like impotence and incontinence. Read more of this newsgroup, read the Phoenix site, read books. Forget about your sex life for a while. Please. Nevertheless, I wish you good luck.
Stephen Jordan - 31 Oct 2004 21:22 GMT Quoting Edward:
>>I have been diagnosed with very little prostate cancer. Out of 14 >>snippets taken during my biopsy, only one showed a trace of just 5%. [quoted text clipped - 4 lines] >>Will some of you be good enough to let me hear from you via email about >>this method? I understand it only kills the cancer cells. Danny replied:
> You left out the other important item- what was the Gleason score. > Persons with serious prostate cancer widespread in the prostate frequently have [quoted text clipped - 5 lines] > newsgroup, read the Phoenix site, read books. Forget about your sex life for a > while. Please. Danny is absolutely correct about the Gleason grade of the sample, and the fact that it's a tiny sample at best.
Other important -- no, *vital* -- factors are:
1. The TNM score. 2. The PSA score. 3. If "free PSA" and/or PAP (prostatic acid phosphatase) were checked, what result? 4. Edward's age and general health.
Edward is entering into a phase of his life in which PCa very well may be a factor as long as he lives. The earlier he begins the struggle, the better are the prospects for good results. And good results often mean simple survival, not necessarily "cure," however it's defined (and there are differences on that point).
As for cryotherapy: Based upon a Gleason 9 score (4+5, 6 of 7 cores, right side), T2bN0M0 (palpable tumor, no lymph node involvement nor metastases), PSA 4.75 diagnosis, at age 67 (good health, otherwise) I underwent cryosurgery on November 20, 2003.
I am not pleased with the result.
Due to rising PSA observed post-procedure, a second biopsy was performed on July 20, 2004. It disclosed that the Gleason 9 tumor was evidently destroyed by the cryo, BUT one of six cores disclosed a Gleason 8 (4+4) tumor at the left base. The urologist's explanation: "we missed it." Swell.
Side effects: IIRC, cryo results in impotence for some 80% of patients. There is a period of time when a catheter must be used to drain the bladder. In my case, it was a suprapubic catheter through the lower abdomen, though a Foley (through the urethra) might be used, instead. I'm a slow healer, and it took a month before it could be removed. Then, the catheter wound leaked for a couple of weeks while it healed. Fortunately, it was not a constant leakage; only when I urinated. Had to wear a gauze pad, though. Yech.
And, yes, I'm impotent.
I have now just completed a course of high-dose radiotherapy known as Intensity Modulated Radiotherapy (IMRT), and presently am on androgen deprivation therapy (ADT). This from an oncologist recommended by the uro, who it seems gave up on me.
Whether any of this will have a good result remains to be seen. As my onc says, we're going to be together "forever." At the beginning, he told me frankly that he had no idea how this would go, as the cryo "threw a monkey wrench" into his evaluation. So far, though, he's pleased. I hardly need say that I am, too. But it remains to be seen whether it worked as desired. He has one other patient who is in much the same situation, though his new tumor did not manifest itself for over a year post-cryo. For privacy reasons, the onc cannot discuss that patient with me, and the patient did not respond to a phone message I left about a month ago. Reason: unknown.
Regarding invasiveness, I'd place cryo between radical prostatectomy and IMRT (most-invasive --> least invasive).
Each modality has its benefits and its risks. Edward has a choice to make and I recommend that, unlike me, he not be stampeded. Study the various treatments (which include "watchful waiting") and select that in which he places the most confidence. Also: do not be afraid to ask exhaustive questions of his physician. Check the various news groups. Go to ustoo.com and explore. He's probably got time to do research.
If he does so, he'll probably be comfortable with whatever decision he makes.
Meanwhile, if he'll supply the info requested above, I'll try to be helpful. So will others. This is a fine group.
Regards,
Steve J __ And, most importantly,
"Never give in--never, never, never, never, in nothing great or small, large or petty, never give in except to convictions of honour and good sense. Never yield to force; never yield to the apparently overwhelming might of the enemy.'' --Sir Winston Leonard Spencer Churchill
hankmackxxxx@usa.net - 31 Oct 2004 23:00 GMT Don't be too hasty to rule either in or out any particular treatment. PC can be a killer. Read Dr Walsh's book, get several opinions, make a decision and go for it. You will find this newsgroup very helpfull. Good luck. ,
Leonard Evens - 01 Nov 2004 02:35 GMT > I have been diagnosed with very little prostate cancer. Out of 14 > snippets taken during my biopsy, only one showed a trace of just 5%. > > I refuse to have the prostatectomy! However, I have heard wonderful > things about the freezing procedure. Cryosurgery does not have a very good track record in the treatment of prostate cancer.
As others have noted, some more information might help us understand your diagnosis. In particular, your age, your PSA level, the Gleason score, and whether or not your doctor felt anything unusual in digital rectal examination are all important.
Patrick Walsh's book Guide to Surviving Prostate Cancer is a good source of information. Don't reject any form of treatment, including surgery, until you understand all the advantages and disadvantages of all of them.
> Will some of you be good enough to let me hear from you via email about > this method? I understand it only kills the cancer cells. > > Thank you for your help in this matter. > > Edward Robert Austin - 01 Nov 2004 03:35 GMT >I have been diagnosed with very little prostate cancer. Out of 14 >snippets taken during my biopsy, only one showed a trace of just 5%. > >I refuse to have the prostatectomy! However, I have heard wonderful >things about the freezing procedure. Hello Edward and all:
Due to my age my doctor leaned toward cryosurgery. So far I am very pleased with the results. As with all other methods of treating PCa only time will tell whether or not it was completely successful.
I don't know what all the good things you have heard about the procedure, I came home the next day and it took a few weeks to recuperate. I've been through worse things but it was not a walk in the park.
As for killing just the cancer cells, in the words of my doctor, "They turn that sucker into a ball of ice, thaw it, and turn it into a ball of ice again. That kills everything except the urethra which is not frozen because of a warm probe kept inserted in it.
Nerves, tissue, everything is destroyed if the procedure is done properly, if not it the Pc may reoccur.
Sex is still wonderful, but is possible only with the aid of a pump.
Regardless of what option you choose, make sure the surgeon is an expert in the procedure. You are welcome to write me privately.
Bob Austin
Age 75 PSA 7 Free PSA 12 1st round of biopsies clear, 2nd. 2 positives Gleason 9 Cryosurgery 03/11/03 Post Op PSA's 0.4 6 Months 0.1 9 Months 0.2 15 Months 0.21
robertbob.austin@NoSpamearthlink.net
jk - 02 Nov 2004 00:08 GMT > I have been diagnosed with very little prostate cancer. Out of 14 > snippets taken during my biopsy, only one showed a trace of just 5%. [quoted text clipped - 8 lines] > > Edward Kind of like being a "little" pregnant Ed.... whatever you do short of nothing, will kill the and/or get rid of your prostate. Thus..... no more ejaculating, possibly incontinence, and erectile dysfunction. Pick your poison, and choose to life!
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JK Sinrod Sinrod Stained Glass Studios www.sinrodstudios.com Coney Island Memories www.sinrodstudios.com/coneymemories
Ed Friedman - 02 Nov 2004 21:20 GMT > Kind of like being a "little" pregnant Ed.... whatever you do short of > nothing, will kill the and/or get rid of your prostate. Thus..... no more > ejaculating, possibly incontinence, and erectile dysfunction. Pick your > poison, and choose to life! Actually, intermittent triple androgen hormonal blockade is also an option. There are no 15 year statistics available yet, but for patients with stage T1-3, with an average PSA of 12.7 and an average Gleason score of 6.6, the results after 8+ years is no prostate cancer (or treatment related) deaths yet reported for the 109 patients involved in that study. 0% for 8 years is a far better death rate than that reported for any surgery or radiation studies, even though those are usually performed on patients with much lower PSA's.
Ed Friedman
jk - 03 Nov 2004 00:00 GMT > > Kind of like being a "little" pregnant Ed.... whatever you do short of > > nothing, will kill the and/or get rid of your prostate. Thus..... no more [quoted text clipped - 11 lines] > > Ed Friedman Sorry I assumed you were leanming toward getting rid of it forever, as opposed to starving it, with your fingers crossed, and no sex drive. Unless your Gleason is high, almost anything you do, or don't do, will probably leave you alive and kicking in 10 years anyway.
 Signature JK Sinrod Sinrod Stained Glass Studios www.sinrodstudios.com Coney Island Memories www.sinrodstudios.com/coneymemories
Alan Meyer - 04 Nov 2004 06:02 GMT > > Kind of like being a "little" pregnant Ed.... whatever you do short of > > nothing, will kill the and/or get rid of your prostate. Thus..... no more [quoted text clipped - 11 lines] > > Ed Friedman Ed,
I hadn't seen that. Have you got a citation for it?
It's surprising to me and makes me wonder if HT is being properly applied to most patients. Most of the people who have died after RP or RT have also had HT, but it didn't save them for 8 years as this study claims to have done.
Perhaps the usual methods of giving hormone therapy are less effective than the "intermittent triple androgen hormonal blockade" that you cite here. If that's true, it's a very important fact that people who have failed RP or RT should know.
Thanks.
Alan
Stephen Jordan - 04 Nov 2004 06:44 GMT Quoting Ed Friedman:
>>Actually, intermittent triple androgen hormonal blockade is also an >>option. There are no 15 year statistics available yet, but for patients [quoted text clipped - 4 lines] >>for any surgery or radiation studies, even though those are usually >>performed on patients with much lower PSA's. Alan responded:
> I hadn't seen that. Have you got a citation for it? I'd like to see it, too. That regimen, or something very much like it, might be efficacious in my case.
> It's surprising to me and makes me wonder if HT is being > properly applied to most patients. Most of the people who [quoted text clipped - 6 lines] > a very important fact that people who have failed RP or > RT should know. The drugs used for triple blockade (ADT3) are a LHRH agonist such as Zoladex®, an anti-androgen such as Casodex®, and finasteride (Proscar®). Strum reports good results, especially from the intermittent course of treatment (NB: Proscar® is continued during the "off" period).
The results had better be good; that's a very expensive menu.
Strum has written, "ADT is a management issue that continues to be hotly debated (@ 2002 -- SJ), and little agreement on the optimal form of ADT has been reached." He recommends a thorough discussion with one's physician, as well as careful research by the patient, before embarking on a course of ADT treatment. Which I intend to do, although I'm presently on ADT1, a LHRH agonist, solely.
BTW, ADT2 is a LHRH agonist + an anti-androgen.
Regards,
Steve J __ "Never give in--never, never, never, never, in nothing great or small, large or petty, never give in except to convictions of honour and good sense. Never yield to force; never yield to the apparently overwhelming might of the enemy.'' --Sir Winston Leonard Spencer Churchill
Leonard Evens - 04 Nov 2004 15:42 GMT >>> Kind of like being a "little" pregnant Ed.... whatever you do short of >>>nothing, will kill the and/or get rid of your prostate. Thus..... no more [quoted text clipped - 30 lines] > > Alan Keep in mind that there is a vast difference between treating (a) patients who have just been diagnosed through PSA testing followed by biopsy and (b) those who have had a primary treatment such as surgery and radiation and subsequently had a PSA recurrence.
First, for patients in category (a), the disease is at a much earlier stage, probably at least 5 years earlier. Most of these patients would be doing fairly well for five years even without treatment. Second, patients are put on HT after PSA recurrence because it is believed that their cancers have metastasized. That selects out an even higher risk population from all those treated by surgery or radiation.
It should also be noted that even for patients with PSA recurrence, there is some difference of opinion about when to begin HT. Many experts think it should be started immediately, but Walsh seems to think that it should be delayed until clinical symptoms of metastatic cancer develop. I believe that there may be some recent evidence that starting it earlier may prolong life, but it is by no means settled yet.
So this is really a comparison between apples and oranges.
Use of HT as a primary treatment for early prostate cancer is not generally recommended by the great majority or urologists or others treating prostate cancer. If I understand Strum, for example, even he seems to be recommending it for cases where there is a good chance the cancer has already spread because of relatively high PSA and high Gleason score. Such therapy might be appropriate in specific cases, but a typical patient with moderate PSA and Gleason in the range 5-7 probably should still consider either radiation or surgery. But note that often a short term use of HT is recommended in combination with radiation because it seems to make the cancer cells more susceptible to radiation damage. I believe they are now trying to determine the optimum amount of HT to use in such circumstances.
Ed Friedman - 04 Nov 2004 20:33 GMT > Keep in mind that there is a vast difference between treating (a) > patients who have just been diagnosed through PSA testing followed by [quoted text clipped - 7 lines] > their cancers have metastasized. That selects out an even higher risk > population from all those treated by surgery or radiation. Leonard,
What you say about the disease being at an earlier stage for patients recently diagnosed (a) vs. those having failed local therapy (b) is true. However, can you produce any reference for a study of patients (a) whose starting PSA is around 12.7 in which no prostate cancer related deaths are seen after 8 years other than the Leibowitz and Tucker study?
Ed
Leonard Evens - 04 Nov 2004 21:40 GMT >> Keep in mind that there is a vast difference between treating (a) >> patients who have just been diagnosed through PSA testing followed by [quoted text clipped - 17 lines] > related deaths are seen after 8 years other than the Leibowitz and > Tucker study? I haven't searched the literature on that speicific question, so the answer is that I can't. But I don't see the significance of that. Patients with prostate cancer who start off with a PSA greater than 10 are at increased risk of metastatic cancer in any case. You would expect a significant number of such patients who are treated with RP or radiation to suffer treatment failure. If they don't receive followup HT, some of them will die. Presumably the argument for the Liebowitz approach is that for such men, an appropriate kind of hormone therapy started very early is superior to waiting for symptoms to appear. From my reading, I believe there is controversy about that.
It is important not to focus in on one particular study. In time these matters will be settled.
If you constructed your model purely as an intellectual challenge, then you should certainly pursue the matter and submit your paper for publication. You may make an important contribution. But if part of the motivation is to deal with your own actual or potential prostate cancer, I think you may get into trouble. You know the saying that a doctor should not treat himself. The same applies when doing research. If you are personally involved in this way, it is very hard to be objective. You should avoid making decisions on your own medical care based on what you think you have uncovered as a researcher.
> Ed Ed Friedman - 05 Nov 2004 19:24 GMT > If you constructed your model purely as an intellectual challenge, then > you should certainly pursue the matter and submit your paper for [quoted text clipped - 5 lines] > objective. You should avoid making decisions on your own medical care > based on what you think you have uncovered as a researcher. Leonard,
Thank you for your concern. I have already made the decision that if I have a growing prostate cancer, no matter what the stage or gleason score, I will be going to Dr. Leibowitz and Dr. Tucker for treatment. I consider that the chance of their patients developing growing prostate cancer (PCa) in the future is small, but remote. I believe that I can improve on their treatment slightly to bring that chance to close to being impossible. Also, I predict that their followup optional treatment of high dose testosterone replacement therapy will result in enormous increases in the life expectancy of those patients who avail themselves of it. I only wish there were some way to get their final treatment without first having to get PCa.
As a mathematician you can appreciate that sometimes a model takes on a life of its own. This is the case with what I am doing. PCa is full of intriguing studies that seem full of contradictions, e.g., biphasic response of LNCAP to T and DHT, studies showing that T promotes PCa, studies showing that T kills PCa. As I study the literature I am learning new things almost daily. The best part is when the model is complete enough to start making predicitions. Then finding that experiments have already been done that verify what you had just predicted is a great thrill. At this point I am writing my first draft. Every experiment on early stage PCa that I can find is consistent with my model (the last little piece fell into place last night).
Ed
Ed Friedman - 04 Nov 2004 20:27 GMT > Ed, > [quoted text clipped - 14 lines] > > Alan Alan,
Before answering your questions, let me give you a little information about my background. I received a Ph.D. in Biophysics and Theoretical Biology from the University of Chicago in 1993, but since then have been working as a computer specialist and just doing theoretical modeling in my spare time. I became interested in prostate cancer when I had a spike in my PSA in May of 2004. I have become so fascinated by this topic that I am currently preparing a paper for submission detailing an entire theoretical model for early stage prostate cancer. I have shown my model to three major faculty members at the University of Chicago - the current chairman of Health Studies, the former chairman of Theoretical Biology, and a doctor in Geriatrics who is currently doing research in prostate cancer. None of them could fine any flaws in my model, and all of them urged me to publish it as soon as possible.
As part of my research, I have come across fascinating articles which are not part of the general knowledge of the public (or most doctors), but which are predicted by my model.
To answer your specific questions, there are two reasons that HT does not work for 8 years when used by most doctors. First, what kills the patient is the growth of androgen independent prostate cancer(PCa) cells. The more total PCa cells you have, the more likely you are to have mutations that are androgen independent. In the study I was talking about, hormone therapy was started early in order to minimize the total number of PCa cells and thus minimize the chance of any of them being androgen independent. The reference to this paper is http://theoncologist.alphamedpress.org/cgi/content/full/6/2/177 I have been in contact with the authors, and since that paper was published, 1 of the 110 patients was found to have ductile adenocarcinoma and has since died of his cancer. Of the 109 other patients with primary prostate adenocarcinoma, there have been no PCa related deaths, and none currently in danger of dying from it.
Also, they have saved lives of patients who have failed RP or RT, by using a similar initial treatment coupled with antiangiogenic drugs. If you want to take the time to sift through 256 slides, you can see for yourself some such patient records by going to: http://www.prostateweb.com/ppt/Fullerton_March_23_2004.ppt
Also, I have been unable to loate any article that has shown that T promotes prostate cancer growth, except when it is converted to DHT. This means that doctors are aiming at the wrong target when they try to minimize T. The only reason that it is effective at all is because it lowers the level of DHT. The most recent reference that illustrates this is the article at: http://147.52.72.117/OR/2004/volume11/number6/1325.pdf
Ed Friedman
Alan Meyer - 05 Nov 2004 01:16 GMT > > Ed, > > [quoted text clipped - 65 lines] > > Ed Friedman Ed,
Thanks for this extensive response, and thank you for doing this research.
I agree with Leonard that, in spite of the results these doctors are getting, surgery or radiation still seems like a better first line treatment than HT for all but quite old patients. Having had both radiation and HT, I can say that the radiation effects bothered me less than the HT effects and taking hormones for 8, 10 or more years is not something I'd want to do unless I had to. Furthermore, I couldn't help but want to try a curative treatment first, before I chose one that could only delay the growth of the cancer.
However, the PCa community is in desparate need of options for what to do if RP or RT fails. The results these doctors are getting do seem a lot better than the standard results. If they pan out and can be duplicated by others, they are good candidates for setting a new standard.
Personally, if I failed treatment (hasn't happened yet), I'd seriously consider this triple intermittent ADT. I don't see why it would be much worse than the standard Lupron or Zoladex only treatment.
Leonard said:
> It is important not to focus in on one particular study. In > time these matters will be settled. From an academic point of view, I'm sure he's right. But if your life is at stake, as it is for people on HT, there isn't time to wait for all the results to be in and all the dust to settle.
This therapy is an extension of a very standard therapy. The doctors aren't recommending something totally new using mechanisms that are totally new and un- understood. They are taking something that is known to work to some degree, administering the identical therapy, and adding more to it. From where I stand, I'm inclined to think that the risk of wait- and-see may be greater than the risk of jumping in.
But as I so often must say, I'm no expert.
Alan
Alan Meyer - 02 Nov 2004 06:13 GMT > I have been diagnosed with very little prostate cancer. Out of 14 > snippets taken during my biopsy, only one showed a trace of just 5%. [quoted text clipped - 8 lines] > > Edward Edward,
As others suggested, find out what your PSA, Gleason, and staging are. The biopsy result is relatively good (if having cancer can be considered good), but other factors are also important in figuring out how aggressive and advanced the cancer is. Under any circumstances you'll want to spend some time investigating your options, but if all the signs are good, you have still more time.
Your age is also significant. PCa tends to be more aggressive if you get it when you're relatively young.
The two traditional therapies are radiation and surgery. Cryotherapy is a relative newcomer.
I shared your fear of surgery and opted for radiation instead. So far, I've been satisfied with my choice and with the mildness of the after effects. Radiation is painless and I was able to go to work every day that I received it - only taking two days off for each of two HDR brachytherapy procedures I got.
Research radiation and cryotherapy. Research prostatectomy too. If I were you I wouldn't be too quick to rule anything out, or too quick to select one therapy over others.
Another good idea is to meet the people who would perform the procedures. You may find that one of them (the urological surgeon, the cryosurgeon, or the radiation oncologist) inspires more confidence in you than any of the others. That too is a factor in the choice.
Best of luck.
Alan
Steve Kramer - 02 Nov 2004 18:44 GMT Edward,
Having provided merely your biopsy results, I'm guesing that you haven't put a lot of effort into research. As this is a life and death matter, I suggest you do so immediately.
Without your age, Gleason score, PSA, or Stage, there is no way we can even hazard a guess as to what your options are or are not. I can tell you that if you have a Gleason of 5 or 6, low PSA, and a Stage of T1a (which is quite possible with one needle of 14 showing 5%) and are in your 50s or 60s, some here was consider you a damned full for not considering radical prostatectomy.
But, to answer your question, cyro will freeze your prostate killing it and everying in it including your cancer, or that is the hope. There are a few here that have tried it. It seems to have worked for one, maybe not worked for a couple and the others are somewhere in Limbo.
 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 (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50) non illegitimi carborundum
> I have been diagnosed with very little prostate cancer. Out of 14 > snippets taken during my biopsy, only one showed a trace of just 5%. [quoted text clipped - 8 lines] > > Edward Steve Kramer - 02 Nov 2004 18:49 GMT that was supposed to be "some here would consider you a damned fool". Fat fingers.
 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 (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50) non illegitimi carborundum
> Edward, > [quoted text clipped - 26 lines] > > > > Edward Alan Meyer - 04 Nov 2004 06:12 GMT > ... some > here was consider you a damned fool for not considering radical > prostatectomy. ...
I agree it would be a mistake not to consider radical prostatectomy. It is a proven life saver.
But I don't think it would be foolish to conclude, as some do, that it's a mistake for a younger man to choose any other treatment.
I admit that my own experience is still too recent to draw any conclusion from. But so far at least, I'm not sorry I chose radiation at age 57.
Just like prostatectomy, radiation is a proven cancer killer. Like RP, it doesn't always work. Like RP, it can be applied skillfully or clumsily. But when it's done well, I believe it does work.
Unfortunately, in some of us cancer has already established itself outside the area where either RP or RT can reach it. For those men, treatment fails no matter which modality they choose.
Even more unfortunately perhaps, some of us are treated by surgeons or radiologists who don't do a good job and leave some cancer behind.
So picking a good doctor is just as important as picking a good treatment modality.
Alan
Steve Kramer - 04 Nov 2004 17:57 GMT Just so there is no misimpression, including for the new lurkers, I am not stating that Radical Prostatectomy is the only solution. I'm just saying that is should not be dismissed out of hand.
 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 (3 mo) 8/03 (48), 12/03, 4/04 (49), 09/04 (50) non illegitimi carborundum
> > ... some > > here was consider you a damned fool for not considering radical [quoted text clipped - 29 lines] > > Alan Alan Meyer - 05 Nov 2004 01:01 GMT > Just so there is no misimpression, including for the new lurkers, I am not > stating that Radical Prostatectomy is the only solution. I'm just saying > that is should not be dismissed out of hand. I agree with that 100%.
Alan
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