PSA six weeks after radical prostatectomy
My PSA was 7.75 and MRI showed prostate lesion with extension into left nerve bundle, no other areas affected. I decided to have radical prostatectomy. Gleason score was 4+3=7 with minor tertiary gleason pattern 5. Pathology came back clear of additional spread to surrounding tissue. At my six week follow up my PSA was 9.9 and my urologist stated he had never witnessed in over a thousand cases a PSA being higher six weeks after surgery and ordered another test. One week later it was 10.3. He and the oncologist said they had never seen this before. I am now being scheduled for a PSMA Pet scan. Has anyone experienced a similar outcome or seen a similar case?
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Thanks Jim. I'm in southwest virginia and not real close to any of the high rated facilities. The virtual route seems to make sense. Both Cleveland and Cedars are top rated and they obtain your records, evaluate them and deliver a written report usually within two weeks. You'd probably be months getting the same results in person.
No symptoms at all. My PSA was elevated at my yearly physical and that's what started it all.
I have not used a virtual service, but this seems like a good idea. You have a lot of data they can review. Also, their second opinion may be useful to an Oncologist you choose for treatment. I'm sure you have a list of questions for your Urologist next week but if you're like me sometimes after getting home and digesting the consult I have further questions. A virtual meeting with a second party would be a good place to ask these new questions in addition to your Urologist. Good luck and I pray your future treatments will be successful.
Thanks Perry, good feedback
Hi went to receive my results from my PSMA hoping that I had no more than the 3 small lesions had not grown or increased as to allow targeted radiotherapy. It was not to be as I now have spots to lymph nodes , peritoneum & one rib. My Oncologist was as gobsmacked as I was. Straight on the chemotherapy next week which hopefully buys me some time. Good luck to all who are hit with this horrible disease. First detection was 2013 & after 9 good years my luck has certainly deserted me of late. All the best & keep the faith.
Geez. What lousy news. I've seen plenty of posts on this site with people who have had spread who keep it in check via chemotherapy and other drugs. I wish you the best of luck in your treatment and keep fighting this lousy "C".