Do you regret having had a prostatectomy vs. radiation, or vice-versa?
Just wondering whether there are some of you that already had a prostatectomy that they regret, and wish they had instead opted for radiation. Conversely, perhaps others chose radiation, but now regret not having just had a prostatecomy.
I'm currently wrestling with this question beforehand, and there seems a consensus that the curative results are equivalent, so I guess I'm wondering more about side effects and the like.
It might be helpful if you mention how long ago you had the respective procedure, please.
Thanks in advance!
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
Well, again, I am dealing with a "center of cancer excellence" at a university, so I generally trust that, as experienced professionals, they're going to be on top of current research.
Have you some new treatment in mind, by way of example?
( I haven't actually been scheduled for surgery yet, and even then, that won't be carved in stone.)
Big macro view is there is active surveillance, surgical, radiation, and focal therapy options. Each has it's controversies. My local urologist was pushing for surgical/radiation treament. I went to center of excellence robotic surgical urlogist for couple years and later was upgraded to grade group 2 so needed to take some action. Consulting a focal specialist and my research, they suggested tulso pro. I ended doing this in December 2024. Tulso Pro is appropriate for right cases. The point here is my center of exellence urlogist was not expert outside of surgical solutions and had some misconception. My "cure" rate is at 70 to 80 percent. I am will take this chance to kick the can down the road a few more years. Should I need another treatment, I would consider the sbrt MRI-guided LINAC (viewray) treatment for it's precision. there many radiaton treatment options as their are other focal therapy technologies. Same is true with Prostatectomy techniques.
Thank you for taking the time to write down your experience. I wondered a couple things as we are not so far apart in age (63). I am debating the same issue and, at 63, the early word is - up to you, you are right on the edge age wise. My health is very good, active person, family history of no cancer. Gleason 7 (3+4) with cribriform and PNI - in 2 tumors. 2 other tumors Gleason 6.
Did you have PNI or Cribriform? Cribriform is tough to eliminate.
Best of health to you.
I was diagnosed at age 51 and gave RT some serious thought. I opted for RARP in the end (to recent to evaluate outcomes). But I definitely would have chosen RT if I were in my 70s.
Hey Jayhall,
congrats on the Qof Life. can you tell me when you got the RARP? and how old you are???
RARP would be good if it was guaranteed - I wonder if death would have been better.
EBRT would be good if it was guaranteed - I wonder if death would have been better.
SBRT would be great if it was guaranteed - I wonder if death would have been better.
ADT SUCKS - I wonder if death would have been better.
Erections - ha ha
Peyronie disease - gimme a break guys
Sorry - not a cheerleader for this fucked up condition
I got my RARP in early May and I'm 60.
I'm with you. Urologist wants to RARP, Oncologist wants to SBRT. Turned down by Mayo for Tulsa Pro, going to Moffitt for IRE consultation. If that fails, I may let it play out as earlier death may be better than RARP or ADT. I'm 67, 4+3. Still searching for decent alternatives.
You could also try radiation without or only short-term ADT. Would give you better odds than doing nothing.
I did that 39 SBRT with 6 months Lupron on the second-round year after RARP. Came out of that with bowel issues and tinnitus; that was 2016 (still ringing and pooping is no fun). But was undetectable for 8 years.
My point is the treatments have left me in an undesirable state, and I wonder how long I might have enjoyed younger women had I done nothing