What's your radiation therapy experience as a pT3b cancer patient?
At six-months post-RP, and despite having two consecutive post-op PSA test values of < 0.1 ng/ml, my status as a pT3b has seen my urologist write an order for consultion with a radiation oncologist to do 40-days (8 weeks) of radiation therapy, knowing there is about a 25% recurrence of prostate cancer in pT3b patients. Therefore, for you as a same pT3b patient (meaning you had one or both seminal vesicles invaded by the cancer):
1) Did you have radiation therapy?
2) If you had radiation therapy, how soon after surgery did you have it?
3) Were your first two, and any subsequent, PSA values < 0.1 ng/ml (essential "zero"), and you had an order for radiation therapy written by your urologist anyway?
4) After having your 40-days of radiation therapy, did your pT3b cancer return, and if so, how long after your radiation (number of months or years) did it take to return? Or...how long have you been cancer-free with recurrence?
5) What were your side-effect symptoms during and after radiation therapy? I heard you can have excessive fatigue, and temporary or permanent changes with urinary continence as well as rectal/bowel issues that are temporary or permanent. I also heard that flatulence (gas) can be a problem during radiation therapy (after too?).
6) If your cancer came back after radiation therapy, what was your next treatment/therapy?
7) Did you suffer any of the ~5% negative serious side-effects of radiation therapy like bladder cancer or rectal cancer?
8) Anything else I should know?
My urologist was kind of "should we or shouldn't we" do radiation "now" vs "wait" until/if my PSA elevates to 0.2 ng/ml or greater? He is concerned that I am a pT3b with a very high likelihood that my cancer will come back "within" five years (could be next year, or two years, or unto to the full five years...but is likely to come back)...this despite having my first two post-op PSA values at < 0.1 ng/ml.
9) How many of you fellow pT3b patients out there have survived 15 years or more?
I appreciate any/all comments from fellow pT3b patients regarding any/all of the above.
Thanks
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
Connect

@rlpostrp
You are a Gleason 3+4. Your cancer would be very slow growing and the likelihood of you having a reoccurrence is around 60% with pT3b according to documents found by AI, not the 100% Your doctor said. Yes they did find the margins were not clear but radiation can resolve that.. I went back and read other responses you made so I have more information to respond this time, had to go back and re-edit this message.
I know guys with Gleason eight and nine that you’re still around 15, 20 and 30 years later. No reason you can’t be.
With my BRCA2, I am guaranteed to have reoccurrence, but I’m still here 16 years later After four of them. The drugs worked for me.
Even if you have a reoccurrence, you can have radiation, which will keep it under control for even more time.
If you would follow up with ADT and an ARSI it could keep you alive for decades because new stuff is coming out all the time to treat advanced cases.
Don’t let this diagnosis get you down. You have something that’s very treatable with what’s available today, and treatment can keep you alive for a long time. Your main risk is not taking the treatments that are available, that’s something that can shorten life.
@climateguy
I went back and I still don’t see you quoting your Gleason score. Maybe that’s why the doctor says you are high risk. You’re an eight or nine.
You definitely want to find out what was in the biopsy. Were any of these things found in the biopsy like intraductal, cribriform, Seminal vesicle invasion, EPE or ECE (Extraprostatic extensions extra capsular extensions)
Those things can make it more aggressive. You want to know exactly what was found.
When they did the MRI were any tumors found and what were the PIRADS score for those tumors.
The more you know the more you can be involved in your treatment decisions. You learn a lot here and you need to know things so you can discuss them with your doctor.