Prostatectomy or Radiation? Lot of stress over which to choose

Posted by bobby1313 @bobby1313, Dec 2 11:45am

I'm having a lot of stress over which to choose.The more I research the more I'm concerned.

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Hi there.

No huge time intervals wwith me - uncontrollable pain after Pluvicto # 2, did Botox, Colonoscopy (thankfully no cancer, pollups, but they did 'discover' the ulcer and confirmed the fissure. Recommended solution to removing irritant from the areas was colostomy; divert the waste and give the ulcer and fissure chance to heal. That was 6 weeks ago. Still experiencing considerable pain and pressure, and their only solution is more drugs more often. Pallitive Care folks want to do what they do - peddle drugs. Surgeon wants to cut. Oncologist is very fuzzy and I now have a colostomy, etc. and no reduction in pain or pressure. Thanks for your energy, and I pray for healing daily (for myself and other men battling this). Part of my 'issue' is other medical things going on in me - I have Prostate cancer which has metastasized, and a lung condition also requiring much medication. Thanks again and blessings, Michael

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Profile picture for michaelbryan6998 @michaelbryan6998

Hi there.

No huge time intervals wwith me - uncontrollable pain after Pluvicto # 2, did Botox, Colonoscopy (thankfully no cancer, pollups, but they did 'discover' the ulcer and confirmed the fissure. Recommended solution to removing irritant from the areas was colostomy; divert the waste and give the ulcer and fissure chance to heal. That was 6 weeks ago. Still experiencing considerable pain and pressure, and their only solution is more drugs more often. Pallitive Care folks want to do what they do - peddle drugs. Surgeon wants to cut. Oncologist is very fuzzy and I now have a colostomy, etc. and no reduction in pain or pressure. Thanks for your energy, and I pray for healing daily (for myself and other men battling this). Part of my 'issue' is other medical things going on in me - I have Prostate cancer which has metastasized, and a lung condition also requiring much medication. Thanks again and blessings, Michael

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@michaelbryan6998
I am really disturbed by what you are going through. The side effects are just way more than acceptable and I really extend to you my sympathy. I just hope you have some relief soon.

Am I misunderstanding what you have said? You seemed so negative about radiation that I thought that’s when you got the fissure. Did you get it there and it was aggravated by Pluvicto, Or did you actually get it from the second Pluvicto treatment?

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Profile picture for jeff Marchi @jeffmarc

@michaelbryan6998
I am really disturbed by what you are going through. The side effects are just way more than acceptable and I really extend to you my sympathy. I just hope you have some relief soon.

Am I misunderstanding what you have said? You seemed so negative about radiation that I thought that’s when you got the fissure. Did you get it there and it was aggravated by Pluvicto, Or did you actually get it from the second Pluvicto treatment?

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@jeffmarc

I do not know the source of the fissure or ulcer. Rectal surgeon speculates it was caused by the doc who did the latest colonoscopy, but no way to know.
Everyone except the radiation oncologist agrees it was aggravated by Pluvicto. At this point, they will not give me more Pluvicto till Im healed.

Appreciate your concern and sensitivity.

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Profile picture for michaelbryan6998 @michaelbryan6998

4 plus years into Prostate Cancer experience. Had three chemo treatments, two year interlude, radiation directly to. prostate (20 treatments) three years ago, and in February 2025 took Pluvicto - two treatments. Radiation irritated (caused?) fissure and ulcers in rectum. EXTREME pain and pressure. NO relief. Oncologist sent me to colorectal sturgeon to remove irritant (stool passing over fissure and ulcer and irritating them) and of course the surgeon recommended surgery - divert the bowel and eliminate the problem. So, I submitted to a surgery five weeks ago and now have a colostomy bag, etc. for the rest of my life. STill have pain, pressure, and extreme discomfort and pressure.

Problem is that they are still 'practicing,' and two things: (1) they do NOT tell you all the side effectss, and when confronted, the radioactive docs deny any responsibility while (2) every article on the net and in medical communication says that radiation proctitis is a direct result of more radiation, and is irritated by the same drugs they prescribe to manage the pain. =

Instead of curing the problem which they created, the system prescribes more strrong narcotics, more frequently, and the docs get their prescription kickbacks, etc. and patients suffer.

My two cents: remove the prostate and never let them radiate you. There are many pleasurable ways to make love, not just one, and it sounds cold, but consider their situation. The docs cannot do anything that the insurance. ompanies won't pay for, or do it in the prescribed sequence, and NO ONE HAS THE PATIENT'S WELL BEING AS FIRST PRIORITY.

For months now all focus of my treatment has been on pain managment and keeping me drugged - meanwhile, the cancer grows and spreads and we talk about 'will this work?' "Lets try this?'

Praying you have wisdom, a doctor not interested in only making money and tikking off boxes. but in seeing you healed fully, and a strong support system for you. "Fight, fight, fight.'

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@michaelbryan6998 So sorry you are going thru this- it sounds absolutely awful. I do have a question, however; why does this colostomy have to be permanent? Can’t it be reversed once the fissure and rectum heal? That should happen but the timeline varies for each individual. Best,
Phil

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I decided to go with surgery earlier this year. I think the main factor for me was the information I was given about how radiation can continue to cause side effects, even new side effects, as well as damage surrounding tissues, months after the treatment. That just didn't sound like the route I wanted to go down. I have been happy with results from surgery overall, hoping that I don't see a rise in PSA which would possibly mean radiation treatments.

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Profile picture for heavyphil @heavyphil

@michaelbryan6998 So sorry you are going thru this- it sounds absolutely awful. I do have a question, however; why does this colostomy have to be permanent? Can’t it be reversed once the fissure and rectum heal? That should happen but the timeline varies for each individual. Best,
Phil

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@heavyphil PS: I suffered with a fissure years ago - with no radiation involved - and until you’ve experienced it, no one can fully appreciate the agonizing pain it causes.
I described it to friends as ‘shitting out barbed wire and broken glass coated with acid’ but even that doesn’t cover it. With radiation on top of it, I can’t even imagine…
Phil

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I chose the prostatectomy in major part because the scans suggested I might have EPE. So I wanted to nail that down. In the event the prostatectomy pathology report said there was none, that my Gleason was 3+4 (my biopsy suggested it'd be 4+3) no positive margins; no affected lymph nodes; no cribiform or intraductal; no metasis etc. But there was +PNI
I felt I was home but a year later I had BCR. And I've been dealing with it ever since. Apparently it was the +PNI that was the culprit in its escape.
I'd still choose the prostatectomy because of all the definitive info I got up front that then made my salvage radiotherapy much more well informed.
Another reason-
the adage I had drilled into my head over half a century ago at Ft Benning training as an infantry lieutenant for Vietnam-
"Lieutenant-always bring the boss bad news first.
Good news takes care of itself."

Good luck!!!

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hi Phil

Yes, in the realm of possibility, the procedure could be reversed. There is cause for optimism.

Blessings,

Michael

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Profile picture for icorps @icorps

I chose the prostatectomy in major part because the scans suggested I might have EPE. So I wanted to nail that down. In the event the prostatectomy pathology report said there was none, that my Gleason was 3+4 (my biopsy suggested it'd be 4+3) no positive margins; no affected lymph nodes; no cribiform or intraductal; no metasis etc. But there was +PNI
I felt I was home but a year later I had BCR. And I've been dealing with it ever since. Apparently it was the +PNI that was the culprit in its escape.
I'd still choose the prostatectomy because of all the definitive info I got up front that then made my salvage radiotherapy much more well informed.
Another reason-
the adage I had drilled into my head over half a century ago at Ft Benning training as an infantry lieutenant for Vietnam-
"Lieutenant-always bring the boss bad news first.
Good news takes care of itself."

Good luck!!!

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@icorps
PNI is extremely common in biopsy results.

I had it my brother had it. I know so many other people that have had it in their biopsies that it doesn’t seem to be a real issue over time.

I would suspect it’s a lot more likely that EPE would be the main issue rather than PNI.

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Profile picture for bobby1313 @bobby1313

Hello everyone.... I'm very grateful for all of the comments, thoughts and experiences that this whole community has shared. As expected,there were sooooo many different experiences.So a quick update on my next steps.... I'm going for a second opinion at Vanderbilt. The Doctor I'm going to is a specialist.... His education is from Mayo Clinic....A Fellowship at Mayo... Masters in Science...and last but not least...an Assistant Professor..... I really think his opinion could help me in many ways.....won't see him until Dec.17th. Will keep y'all posted.Once again, thank you all.

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@bobby1313, how did the second opinion consult go? I'm sure the info the guys shared with you helped you feel prepared for the appointment and equipped with questions to ask. Did the appointment help bring clarity to your decisions? Next steps?

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