Conflicted/Confused, any Guidance/Advice out there?
I will be 61 at the end of this month. MRI on August 2022 revealed an area of suspicion measuring 2.2 cm x 1.4 cm within the left transitional zone mid gland base. Impression from Biopsy September 2022 showed 2.2 cm PI-RADS 5 lesion within the left transitional zone mid gland/base with probable extraprotastic extension. 18 cors pulled 3 were cancerous. Gleason score was given 3+3 but my second opinion stated 3+4. Was told low risk and AS is OK.
Second biopsy Jan 2024 for samples revealed 3+3 and 3+4 Gleeson scores. The report came back with 55 mL gland. Redemonstration of PI-RADS 5 lesion in the left anterior transitional zone with probable ECE. My last PSA in Aug. 2023 was 5.7. I was then told I’m no longer low risk but low intermediate unfavorable. I don’t believe there was any big differences that I can understand for the status change. I was scheduled for external beam radiation this week but chickened out after reading the side effects, especially with a bad baseline for bowel symptoms.
If anyone can make some sense of all of this and provide opinions, I would greatly appreciate it. I am trying to make a decision on what treatment to go with. I’m in the Boston area and we have great Hospitals and Doctors but that doesn’t make the decision any easier.
Thanks and best of luck to everyone.
Interested in more discussions like this? Go to the Prostate Cancer Support Group.
Good to know. I hope I'm a good candidate for Tulsa but won't know until I have my consultation.
I wish you the best of luck. Take care!
RP is not just for younger guys. At 74, G9, CR , aggressive and advanced, my UCLA doctors recommended 6 months ADT and Erleada, then Robo surgery, then 6 more months of the same drugs. I started this 30 months ago and my PSA remains at .01. I am hoping for the best, however, I think my UCLA doctors gave me good advise and good service for a difficult PC case
This is interesting. So you did ADT before RP? I might ask about this at my next appointment. I don’t want to role the dice but could use a little time deciding. I feel incredibly pressured to make a choice. As I mentioned in one of my other posts, I should have been doing my research earlier. I want to feel like I’m making the right choice. Thanks for sharing your story. Everyone in this group has been most helpful. Best of luck to you.
72 @ RP 2022
I had excellent surgical experience and postop recovery. Would elect surgery again.
However, others have done well with radiation.
Information is that outcomes are similar.
Best of luck to you with your challenging decisions.
Batsam 10, My treatment was part of an Erleada clinical trial for high risk cancers and meds before RP was not then SOC. My surgeon recommended the clinical trial for me because the meds before surgery made the tumors smaller and gave the surgery a better chance of success
OK, understood and wishing you the very best outcome. Take care.
I recommend reading the PCF.org and PCRI.org information on exactly this situation and also get an opinion from a radiological oncologist that specializes in prostate cancer. You still have time to make the right decision for you and those resources provide an unbiased summary of risks and benefits of both treatment options. Also consider a scan to check for the spread of cancer outside of your prostate, as this may affect your decision or surgery versus radiation. There are also two books that help to guide you through this decision (Dr Patrick Walsh and another by Dr. Mark Schultz).
I have been watching the pcri videos which are great. I like Dr Schultz and wished he was in my area. I have reached out to their help line. I’ve asked about a scan and all of the urologists I have seen say they don’t do scans for Gleeson 7 which I’m not happy about. It would help on making a decision. It could be an insurance issue that they are aware of. Thank you for posting and sharing your information.
It is probably an insurance issue. Before my clinical trial started they directed me to do a PET scan and when I went in for it, the attendant told me that it was not covered by insurance and it would cost $3,000. I paid that and afterwards successfully argued with medicare and blue cross. Good luck to you, this cancer stuff is more than irritating