Medical Forum / Diseases and Disorders / Prostate Cancer / November 2007
just got back from Uro
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fatcat - 06 Nov 2007 17:11 GMT Thank you to everyone for all the information and support. Had a Ct scan and MRI, blood work, just got the results. Everything fine except gallstones, psa stable, further Biopsy showed DNA shows slow growing. confined to one small section. Since I'm 59, healthy, a little overwiehgt, lost 60 lbs so far. Will see raidology oncologist (sp) later this week. My Uro who does Cyro, did not recommend it, due to age and possible side effects, he said any of the approved, to include W W, would work for me with basically the same results except W W. It would be up to me. Leaning strongly toward Surgery laproscopic (sp). He would send me to Atlanta, would have to drive about 4 hours oneway, have friends in Atlanta. Side effects bother me a little. Will wait on final choice after seeing Radologist, he is local, get to stay home. Any thoughts between the 2 methods, Surgery or Radiation. Choice on the radition is IGRT or Seeds. Thank You again for everything
djperry42@sbcglobal.net - 06 Nov 2007 18:08 GMT I'm a little confused about the "DNA" - do you mean Gleason? Also, congratulations on having a uro who's honest - didn't recommend Cyro (you mean Cryo?) even though it would help him make his next BMW payment. As for the treatment you finally opt for, if you ask this group you're going to get biased opinions on all sides with little clinical evidence to support one treatment being significantly better than another. You just have to look in the archives to find every argument for all sides - they're all there many times over. I think the most useful thing to consider is the possibility that you might end up with side effects and to decide on which side effects would be the most tolerable for you. In my case, I opted for laparoscopic surgery for two reasons. First off, I had throat surgery many years ago that left me with a scar that is numb to this day and I get the heebie-jeebies anytime I or someone else touches it. That's just me, go figure. I didn't want another running up my belly. Secondly, a side effect of radiation is bowel problems up to and including fecal incontinence, especially since that part of my anatomy is already delicate to start with - hemorrhoids for instance. Yeah, I know you rad types are going to pooh-pooh it (pun intended) because it's so rare but any possibility greater than zero is more than I wanted since brown diapers will pretty much preclude any social life except among a very few closest friends who would deserve a special place in heaven for their understanding. As it turned out, I do have urinary incontinence which isn't a big deal for me and little Willie only functions marginally even with all the crutches - pills, pumps, shots, et al. Best of all though, and really the only thing that counts is my PSA is still <0.1 at four years, three months post-op.
Good luck with whatever treatment you choose and hopefully you won't have any side effects at all. Keep us posted on your progress. Dave Perry
> Thank you to everyone for all the information and support. Had a Ct > scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 10 lines] > Any thoughts between the 2 methods, Surgery or Radiation. Choice on > the radition is IGRT or Seeds. Thank You again for everything I.P. Freely - 06 Nov 2007 20:40 GMT > a > side effect of radiation is bowel problems up to and including fecal > incontinence, especially since that part of my anatomy is already > delicate to start with - hemorrhoids for instance. Yeah, I know you > rad types are going to pooh-pooh it (pun intended) because it's so > rare Walsh and others disagree with it's being that rare; I'd research the short and long term bowel problem severities and likelihoods closely. IMO, bowel hassles would vastly exceed my moderate urinary incontinence.
I.P.
djperry42@sbcglobal.net - 06 Nov 2007 20:55 GMT I didn't want to start another war on this issue so I thought I'd just mention it and let Fatcat investigate for himself. I've seen studies that indicate long term bowel side effects of radiation as high as 20%. I don't know how many of these are incontinence but 20% is way too high for my tender blowhole. Dave Perry
> djperr...@sbcglobal.net wrote: > > a [quoted text clipped - 9 lines] > > I.P. Steve Jordan - 06 Nov 2007 21:20 GMT On November 6, Dave Perry wrote:
> I didn't want to start another war on this issue so I thought I'd > just mention it and let Fatcat investigate for himself. I've seen > studies that indicate long term bowel side effects of radiation as > high as 20%. I don't know how many of these are incontinence but 20% > is way too high for my tender blowhole. Well, there are different types of RT with different SEs.
I can't find anything that says 20%, even for all rectal SEs, and especially for current RT methods, but maybe I'm not looking in the right places.
Can Dave cite his source?
Thanks.
Regards,
Steve J
djperry42@sbcglobal.net - 07 Nov 2007 17:55 GMT There are plenty of sources citing 5-20% bowel problems post radiation therapy. Most of these are rectal bleeding and pain. Bowel incontinence seems to hover around the 2% level. Go to Pub Med and do a search. One interesting study can be found by typing in 17497319. That's the PubMed ID number. This is a study that looks at bowel problems 15 years after EBRT. Granted there are more advanced techniques today with much lower levels of bowel toxicity but it's interesting to see what those poor buggers are going through at the 15 year mark. Patients answered various questions involving QOL issues and one response was quite striking. "Quite a Bit/Much" stool leakage was reported by 20% of the patients at the 15-year followup. And in another response, 39% reported no bowel problems (apparently 61% did.) I'm sure more recent patients with all the 3-D's, conformals, et at will fare better at the fifteen year mark.
As for myself, I'm not concerned with whether it's 0.2% or 20.2%. Any percentage higher than zero for bowel issues is more than I want to deal with, especially since I'm one of the 2% who had a SE with a vasectomy, one of the 5% who has urinary incontinence and one of the 50% with a limp Willie with prostatectomy. Not a good track record. It's 100% if it happens to me. Dave Perry
> On November 6, Dave Perry wrote: > [quoted text clipped - 17 lines] > > Steve J Steve Jordan - 07 Nov 2007 19:01 GMT On November 7, Dave replied to me:
> There are plenty of sources citing 5-20% bowel problems post radiation > therapy. Most of these are rectal bleeding and pain. Bowel > incontinence seems to hover around the 2% level. (snip)
OK, we're actually on the same page, as the particular topic was bowel incontinence, not the overall "bowel problems," which can, as Dave and the article mention, cover a wide variety of situations. I searched only for bowel incontinence.
A problem with the study Dave cited, as is the case with so many retrospective surveys, is that the RT procedures were performed several years prior to the survey. I don't believe that those procedures are in use at this time, at least not in the modern world, great strides in accuracy and preservation of uninvolved tissue having been made.
One example is a friend of mine who is a 15-year PCa survivor. Initially, 15 years ago, he was offered whole-pelvis RT and declined.
Dave did mention that modern methods are better, and I think that we all should bear that in mind when reading such studies.
It's like the oft-repeated claim that chemotherapy offers only a few months survival at best. But what is ignored is the fact that the brave and selfless men who participated in the clinical trials were for the most part on their last legs and had no hope. IOW, they were in the worst possible condition and those of us who start chemo earlier can reasonably expect better results.
> As for myself, I'm not concerned with whether it's 0.2% or 20.2%. Any > percentage higher than zero for bowel issues is more than I want to > deal with, especially since I'm one of the 2% who had a SE with a > vasectomy, one of the 5% who has urinary incontinence and one of the > 50% with a limp Willie with prostatectomy. Not a good track record. > It's 100% if it happens to me. True enough, and I wish Dave well.
Regards,
Steve J
Steve Jordan - 06 Nov 2007 21:08 GMT On November 6, Dave Perry replied to "fatcat":
(snip)
> ...................Secondly, a > side effect of radiation is bowel problems up to and including fecal > incontinence, especially since that part of my anatomy is already > delicate to start with - hemorrhoids for instance. Yeah, I know you > rad types are going to pooh-pooh it (pun intended) because it's so > rare but any possibility greater than zero is more than I wanted..... Here's some science:
Florino C et al., "Clinical and Dosimetric Predictors of Late Rectal Syndrome after 3D-CRT for Localized Prostate Cancer: Preliminary Results of a Multicenter Prospective Study."
Int J Radiat Oncol Biol Phys. 2007 Sep 17
PubMed ID: 17881142
Fecal incontinence was experienced by 15 of 1132 patients, which is 1.32%.
PubMed, a division of the National Institutes of Health is at www.pubmed.gov
Anecdotes: Two friends have undergone image-guided RT (IGRT) also called Tomotherapy. The rad onc says that the radiation exposure is shaped such that the rectum is spared. Neither of my friends has complained of any fecal incontinence. YMMV, of course.
(IGRT is a refinement of IMRT)
Regards,
Steve J
BH - 06 Nov 2007 18:23 GMT You will probably get several lengthy responses on the question of surgery vs. radiation, so I'll keep mine short. Generally, if one has surgery first, and it fails (PSA starts rising again) the option of radiation is still available. If one chooses radiation first, the possibility of surgery later (in case the radiation fails) is at least reduced. That's because the radiation can affect surrounding tissue (colon, bladder, etc.) and leave scar tissue that makes surgery difficult, at best. I don't know if seeds can cause that sort of damage, or not. Someone else will have to address that.
Regarding your earlier question about riding a motorcycle, if you are riding any kind of fairly comfortable street bike, you'll have no problems after the surgery heals - if you choose surgery. Radiation would cause no problems at all. If you have incontinence issues, that might be exacerbated by a motorcycle saddle, though. But, that's also manageable.
I also had my gall bladder removed a few years ago. If you need any thoughts on that, let me know by email and I'll share my experience that way - to keep it out of the PCa group. My body's reduced ability to handle fat after the removal of the gall bladder does, I think, add to affects of radiation on my colon, though. That presents some interesting and unplesant problems sometimes!
BTW, I grew up in Watkinsville, a small town about 7 miles south of Athens. I now live in WA.
Good luck! Burney
>Thank you to everyone for all the information and support. Had a Ct >scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 10 lines] >Any thoughts between the 2 methods, Surgery or Radiation. Choice on >the radition is IGRT or Seeds. Thank You again for everything RP in 1995 (age 52) RT in 2000 ADT (Casodex) 10/06 - 8/07
burney dot huff at mindspring dot com
Peter - 06 Nov 2007 19:29 GMT Hi fatcat,
Sounds like you are well on your way of information gathering and making your best shot at making a decision regarding your treatment. I will speak to your concerns of surgery in Atlanta and the side effects of laparoscopic surgery. Again, these are my personal anecdotal experiences but they may be similar to your own.
My experience with the robotic lap. radical prostatectomy is such that if you had a place to stay directly after hospital discharge would be great. I live 2 hrs away from NYC where the surgery took place. I spent the first night at my mom's house 40 min away. The town car ride was bumpy and I felt ok to be out of the hospital. Wasn't quick on my feet but being in a comfort zone helped. I was walking a few blocks the first day, 1/2 mile the second. Only stopped when I saw red colored urine in the catheter tube. Freaked me out, was told that it was no problem. Having some contacts with simple questions also was nice. As far as the side effects with the robotic lap. the effects seem to be easing a bit. My surgery was only on 10/13 so this is good news for me. My erectile response is returning nicely except I am concerned that my experimenting with self arousal may be early. I can achieve a erection and orgasm but I probably should ease up and wait a bit more. Urinary issues are easing a bit but more slowly. I am dry all night and when I am standing/ walking I leak more. I go through a few diapers a day supplemented with sanitary pads. I practice the Kegels and expect there will be a change towards drier soon. Hope that my experiences shed a light on the darkness of your predicament. If my health rebound is any light in the darkness, I feel my experience has been positive so far and I would do the same path over again. Good luck, Peter I choose the surgery for the reason given that side effect will improve with time after the surgery, radiation is the opposite in that symptoms could get worse with time.
> Thank you to everyone for all the information and support. Had a Ct > scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 10 lines] > Any thoughts between the 2 methods, Surgery or Radiation. Choice on > the radition is IGRT or Seeds. Thank You again for everything ron - 06 Nov 2007 19:31 GMT On Nov 6, 10:11 am, fatcat <d127geng...@embarqmail.com> wrote...snip...
> Any thoughts between the 2 methods, Surgery or Radiation. fatcat...There are now (at least) 5 peer-reviewed papers that have been published and suggest that surgery has an edge over radiation in terms of outcome in the treatment of PCa; in 4 of the 5 studies at least one of the authors is an established PCa researcher and the publication occurs in a major journal.
The following long-term studies compare RP, RT and WW: Urology. 2006 Dec;68(6):1268-74; Long-term survival probability in men with clinically localized prostate cancer treated either conservatively or with definitive treatment (radiotherapy or radical prostatectomy); Tewari A, Raman JD, Chang P, Rao S, Divine G, Menon M. J Urol. 2007 Mar;177(3):911-5; Long-term survival in men with high grade prostate cancer: a comparison between conservative treatment, radiation therapy and radical prostatectomy--a propensity scoring approach; Tewari A, Divine G, Chang P, Shemtov MM, Milowsky M, Nanus D, Menon M. J Urol. 2007 Mar;177(3):932-6; 13-year outcomes following treatment for clinically localized prostate cancer in a population based cohort; Albertsen PC, Hanley JA, Penson DF, Barrows G, Fine J. Arch Intern Med. 2007 Oct;8;167(18):1944-50; Short- and Long-term Mortality With Localized Prostate Cancer; Merglen A, Schmidlin F, Fioretta G, Verkooijen HM, Rapiti E, Zanetti R, Miralbell R, Bouchardy C.
The following reference just compares RP and RT: J Clin Oncol. 2003 Jun 1;21(11):2163-72; Cancer-specific mortality after surgery or radiation for patients with clinically localized prostate cancer managed during the prostate-specific antigen era; D'Amico AV, Moul J, Carroll PR, Sun L, Lubeck D, Chen MH
That said, if your GS is valid and with only 1 stick out of 13 positive, I doubt that you will see much of a difference between RT and RP in your case. Consider the following points in making your decision: 1. Select a treatment based on the best doctor available to you. 2. Compare the long-term side effects (SEs) likely to occur from each treatment and select a treatment based on your sensitivities. Note that RT SEs may take up to 6 years to show up. The following references may be useful: http://www.medscape.com/viewarticle/548683_print J Clin Oncol. 2005 Apr 20;23(12):2772-80; Long-Term Outcomes Among Localized Prostate Cancer Survivors: Health-Related Quality-of-Life Changes After Radical Prostatectomy, External Radiation, and Brachytherapy; Miller DC, Sanda MG, Dunn RL, Montie JE, Pimentel H, Sandler HM, McLaughlin WP, Wei JT. 3. The length of the membranous urethra, as determined by endorectal MRI, appears to correlate with post-RP return to continence (J Urol. 2002 Sep;168(3):1032-5; Urinary continence after radical retropubic prostatectomy: relationship with membranous urethral length on preoperative endorectal magnetic resonance imaging; Coakley FV, Eberhardt S, Kattan MW, Wei DC, Scardino PT, Hricak H.); if yours is short, well, just something else to consider in advance, if possible. 4. If RT is your choice, then a) have your AUA score measured [it's a written test], if it is high, RT will only make your urinary symptoms worse; b) RT is contra-indicated for any small vessel disease such as diabetes mellitus (there is a higher liklihood of RT SEs with diabetics than non-diabetics) and c) discuss the likelihood of seconday cancers with your rad onc, while the risk appears to be a few percent ten years out from treatment, it is real and should be understood going in. 5. If you consider AS, a color doppler ultrasound or endorectal MRI would be an excellent test to help you confirm that AS is applicable in your case, and also it will be useful as a long-term tracking tool.
...Best wishes and good health, ron
safire - 06 Nov 2007 21:07 GMT > Thank you to everyone for all the information and support. Had a Ct > scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 10 lines] > Any thoughts between the 2 methods, Surgery or Radiation. Choice on > the radition is IGRT or Seeds. Thank You again for everything I understand your Gleason is 3+3 and your PSA is 4.9. Since you're a little overweight, 59, concerned about side effects, if I were you, I would avoid both surgery and radiation, i.e. opt for "observation". Look at the September 2005 NCCN guidelines and you'll see that that is a very responsible decision. Don't let hysterical people scare you that you should "get rid of the beast inside". When there is no compelling reason for treatment, why would you take the considerable risk of side effects?
Steve Kramer - 06 Nov 2007 21:29 GMT > I understand your Gleason is 3+3 and your PSA is 4.9. Since you're a > little overweight, 59, concerned about side effects, if I were you, I [quoted text clipped - 3 lines] > should "get rid of the beast inside". When there is no compelling reason > for treatment, why would you take the considerable risk of side effects? For the most part, I concur with safire. You should research watchful waiting (or active surveillance or its other monikers) and determine if it's good for you. I suspect that you will find that you are too young and that you will want to get the cancer out before it gets out of your prostate. But, if you don't research it, you will always wonder if you should have.
 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 PSAD 0.19 years EBRT 05-07/2002 @ 47 PSA .34 .22 .15 .21 .32 PSAD .056 years Lupron 07/03 (1 mo) 8/03 and every 4 months there after PSA .07 .05 .06 .09 .08 .132 .145 PSAD 1.4 years Casodex added daily 07/06 PSA <0.04, <0.05, <0.04, <0.04 10/11/07 Non Illegitimi Carborundum
Alan Meyer - 06 Nov 2007 22:00 GMT > > I understand your Gleason is 3+3 and your PSA is 4.9. Since > > you're a little overweight, 59, concerned about side effects, [quoted text clipped - 12 lines] > cancer out before it gets out of your prostate. But, if you > don't research it, you will always wonder if you should have. I agree with safire that WW is not unreasonable in your case, but also agree with Steve that your age is a tad on the young side for long term WW. If it takes 10 years for you to develop metastatic cancer, you'll only be 69 at the time, and might die by, say, age 75. I don't have the numbers in front of me, but I seem to remember that 15 years after diagnosis without symptoms is about as long as the average man gets, though some do better. If you were 69 now, or 75 now, that starts to look more attractive than treatment.
However, safire isn't recommending no treatment, he's merely recommending no treatment right now. Watch it and wait and if/when it starts to look like it could become more dangerous, then take action.
In your particular circumstance, this has some special appeal. You are way overweight. If you go on a firm diet and lose 10 pounds per month, in less than a year you'll be in athletic trim - ready for any treatment you might choose. Your numbers look okay for waiting at least that long.
There is apparently some evidence that diet and weight play some role in cancer. How much is not well known. But it's conceivable that getting yourself in shape will slow the growth of the cancer. So that's another benefit of doing that.
Watchful waiting, if you do it, should involve a plan, not the absence of a plan. You should have a plan for how often you will get PSA tests and what threshold of PSA and/or PSA velocity will signal that it's time to get treatment. Your uro should be able to help with such a plan.
I think I would certainly opt for treatment if my PSA went up near 10, which would move you from the "low" to the "intermediate" risk category.
Alan
ron - 06 Nov 2007 22:31 GMT On Nov 6, 3:00 pm, Alan Meyer <amey...@yahoo.com> wrote...snip...
> I agree with safire that WW is not unreasonable in your case, > but also agree with Steve that your age is a tad on the young [quoted text clipped - 5 lines] > If you were 69 now, or 75 now, that starts to look more > attractive than treatment. Hi Alan...I agree with most of what you wrote, but would like to add to the above paragraph. Your numbers are basically correct, but they would only apply to a man with a cancer that will become life threatening during his lifetime. There are many men who are diagnosed today but have an "indolent" cancer that will never become life threatening during their lifetime. If these men seek treatment, then they will become part of the overtreated population.
Prior to PSA screening, it used to be that few men were overtreated and many men died from advanced PCa. Now with widespread screening in the US, far fewer men die from advanced PCa, but many men who would not have had any symptoms during their lifetime and would have died from something other than PCa are now identified and their indolent cancer is treated. Estimates of PCa overtreatment in todays US population range from 10-15% to 60-70%. Personally, from papers I've read (especially Moul's and Klotz's work), I think the floor is around 20%. Here is a recent abstract:
Overdiagnosis and Overtreatment of Early Detected Prostate Cancer; C. H. Bangma, S. Roemeling & F. H. Schr?der; World J. Urology, v. 25 (2007), 3-9
Abstract: Early detection of prostate cancer is associated with the diagnosis of a considerable proportion of cancers that are indolent, and that will hardly ever become symptomatic during lifetime. Such overdiagnosis should be avoided in all forms of screening because of potential adverse psychological and somatic side effects. The main threat of overdiagnosis is overtreatment of indolent disease. Men with prostate cancer that is likely to be indolent may be offered active surveillance. Evaluation of active surveillance studies and validation of new biological parameters for risk assessment are expected...
and an excerpt from the paper:
"The impact of overdiagnosis and unnecessary treatment and of its side effects on patient health is also unclear; however, application of a mathematical model (the Miscan model) on data from the ERSPC has shown that, in an annual screening program for men aged 55-67 years, 56% of diagnosed cases would constitute instances of overdiagnosis [22]. If this estimate proves to be realistic (as it appears to be the case), nationwide screening programs may not be acceptable using the present screening regimens, even if benefits in terms of mortality reduction were shown"
Of course, the rub is that we have no foolproof way to separate men with indolent or "pussycat" disease from men whose PCa will eventually threaten their life. So if one does decide to start along the AS/WW path, vigilance is a must. BTW, AS is not a walk in the park; repeat biopsies, medical tests, etc. There are SEs with AS as well. For many, the psychological stress of the situation becomes to great and they seek treatment.
I don't want this to turn into a screening debate, that's another issue. But there are many young men being diagnosed today who don't need treatment; whose lives become dramatically altered due to SEs resulting from treatment. AS is a valid option for young men to consider if they meet stringent criteria. Just my thoughts...Best wishes and good health, ron
Steve Jordan - 06 Nov 2007 22:57 GMT (snip)
> I don't want this to turn into a screening debate, that's another > issue. But there are many young men being diagnosed today who don't > need treatment; whose lives become dramatically altered due to SEs > resulting from treatment. (snip)
Perhaps.
But *who are they?*
No one knows.....
I don't want some beancounter deciding whether my disease should be treated. That is *my* job, and mine alone.
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.
rosbif - 07 Nov 2007 07:53 GMT >(snip) > [quoted text clipped - 8 lines] > >But *who are they?* Ron S posted up a good link.
GL</=6, T1c-T2a, PSA<10, PSADT >/=3 years, and not 'too young'.
Apparently 42% of these had doubling better than 10 years.
WW (and aliases) isn't a determination to do nothing, ever, but to do nothing for the moment other than staying vigilant. The PSADT above is based on 3 tests in 6 months. Looks like a good plan.
ronju99 - 07 Nov 2007 12:44 GMT The problem with the study is that it was done for patients over 70 years old that one wouldn't expect to live much longer than 15 years on average. For someone as young as Fatcat an assuming a long life expectancy, the study may put one on a course for disaster not knowing how it will play out for longer terms but possibly putting someone in jeopardy of not being able to either have a chance for a cure or waiting too long and not being fit to handle the treatment choice.
Here is the links; http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=ShowDetailView&TermToSear ch=15535443&ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel. Pubmed_RVAbstractPlus
An; http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=pubmed&dopt=AbstractPlu s&list_uids=15582244
Ron S.
rosbif - 08 Nov 2007 21:38 GMT >The problem with the study is that it was done for patients over 70 years >old that one wouldn't expect to live much longer than 15 years on average. [quoted text clipped - 3 lines] >able to either have a chance for a cure or waiting too long and not being >fit to handle the treatment choice. I'd forgotten the study focused only on the over-70s. Even so, despite the total absence of reliable longer term data on younger patients, I don't think it would be reckless for a newly diagnosed at 60 yrs, who could tick all the low-grade boxes, to consider WW for a year or so in order to establish his PSA dynamics. If I looked to be on course for a 10 year doubling time, I'd be inclined to remain on WW until that forecast began to shrink significantly.
ronju99 - 09 Nov 2007 00:22 GMT I agree with you in that if it was me and knowing what I know now, I would monitor my psa doubling time and delay surgery as long as possible and enjoy the fact that I didn't have to deal with side effects any sooner than necessary. However, I would be surprised if he did do active surveillance.
Ron S.
rosbif - 07 Nov 2007 07:50 GMT >> Thank you to everyone for all the information and support. Had a Ct >> scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 18 lines] >should "get rid of the beast inside". When there is no compelling reason >for treatment, why would you take the considerable risk of side effects? Safire, you apparently were a watchful waiter who had surgery (?). What were your stats at diagnosis (commencement of WW) and at what point (time, PSA etc) did you opt for treatment?
Steve Kramer - 06 Nov 2007 21:23 GMT > Thank you to everyone for all the information and support. Had a Ct > scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 9 lines] > final choice after seeing Radologist, he is local, get to stay home. > Any thoughts between the 2 methods, My only thoughts are you are doing really well in your decision-making process. I have nothing otherwise to add with regard to surgery vs. radiation.
SRK
Beverley - 07 Nov 2007 23:08 GMT Here's a few questions to ask your rad-onc.
How many brachytherapies has he done? Does he do them on high PSA's (over 10) and on high Gleason's (7 or more)? How long has he been doing them? What is his success rate? Number of patients with ED, bowel problems, urinary problems? Define ED! (Some figure if they use Viagra and are successful then they don't consider it ED) How many years does he follow-up with his patients?
Our brachy doc has been doing them since 1989. He does between 5 to 10 per week. (He's at a huge teaching hospital and at a large Veteran's facility.) He can count the number of ED patients on less than ten fingers. (He considers anything less than natural spontaneous erections as being ED) No bowel problems and the number patients with long-term urinary problems are under 20. (The common urinary problem is difficulty starting the stream and for most men the problem vanishes as the prostrate is destroyed. It is correctable with meds and only a few have a problem after about 18-20 months) He does not do anyone over a PSA of 10 or a Gleason higher then 6. He follows them as long as they are alive. His average patient gets 121 of Iodine-125 seeds. He has not had a single failure in all those years! He admits he's waiting for the shoe to drop, but says he's not alone as there are plenty of doc with the same statistics.
One of the big objections to brachytherapy is the concept that it if doesn't work you have no further recourse. 5 weeks of EBRT followed by brachytherapy is equivalent to a RP with salvage radiation. If that doesn't get it then the RP with salvage radiation wasn't going to get it either!
Brachy can be done without the added EBRT, and the EBRT will still be an option later if required.
My husband had a combination of EBRT on the IMRT and brachytherapy (Gleason 6 (3+3) PSA 4.9 and fPSA 8.9% , he was 56 when the treatment was started.) Five years later, my husband was a postmortem organ donor and they purposely searched looking for cancer cells related to his PSA. He did not have a single cancer cell to be found in his body.
Brachytherapy does work! My husband missed almost nothing in the way of time from work. He went each morning before work for his EBRT and then missed the day (Friday) they inserted his seeds (brachytherapy). He came home and unwillingly played couch potato as he felt just fine. He did admit it was fun being spoiled. You are supposed to stay very quiet after brachy for about 3 days so that you don't lose a seed.
The other myth that needs de-bunking is the concept that you will be radioactive for a while. Apparently you can set off the metal detectors at an airport, etc. and I've heard others say they have asked the doctor for a note if they travel, etc.. But you are not going to damage your wife or child/grandchild with radioactivity. The seeds "reach" only a quarter of an inch with true radioactivity. You could slap a radiation badge on your wife's pelvis and sleep snuggled and she will never register on the badge.
Some docs will cover their a.s and tell a patient to not hold a baby for the first 6 weeks. Our doc was a nuclear physicist before he got is MD in '89. He was part of the govt's nuclear regulatory panel and he swears it is perfectly safe. He says if you don't feel comfortable then don't do it. I know they load the seeds by hand and all of the docs and their residents wear "a ring" on their finger to detect radioactive exposure. They have direct exposure to the seeds all the time and they've never had a problem.
As with any PC treatment if you still were entertaining the idea of more children then you should consider banking your sperm before treatment. Brachy will eliminate ejaculate as most of the fluid produced is made in the prostrate. Unlike RP where the vas are cut, during brachy they do remain somewhat intact so it seems as if it would be possible to pass sperm.
Some men complain about dry orgasms both after RP or RT. It's different. My husband never complained, but he did admit it was an odd sensation. Although he said it was still satisfying.
RCOG is in Georgia and somebody out here had brachy done by a doc trained at RCOG but had left to start is own practice. Wish I could remember who it was. Maybe Steve might know.
If you are a Vietnam vet you are instantly covered through the VA system. The trick is to apply for the coverage. (yes, they pay you money and they will pay for the treatment. If you need help with that let me know as I still have that information.
Please contact me if you have any questions! Bev
> Thank you to everyone for all the information and support. Had a Ct > scan and MRI, blood work, just got the results. Everything fine except [quoted text clipped - 10 lines] > Any thoughts between the 2 methods, Surgery or Radiation. Choice on > the radition is IGRT or Seeds. Thank You again for everything ron - 08 Nov 2007 02:26 GMT On Nov 7, 4:08 pm, "Beverley" <beverly.brow...@verizon.net> wrote...snip...
> RCOG is in Georgia and somebody out here had brachy done by a doc trained at > RCOG but had left to start is own practice. Wish I could remember who it > was. Hi Bev...Dr F. Critz was the head guy at RCOG, he had a falling out with his two assocoiates. Ham Williams still practices in the area, can't remember the other guys name. They are top-notch...Best, ron
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