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Just a minor point about EBRT/IMRT. I was on ADT beginning June 07, then radiation in Sept & Oct 07. All 12 biopsy samples were 5 to 70% PC, the Gleason was 9, the PSA went from 8 to 14 in 8 months. MRI, CAT, rad bone scan, all negative for pc outside prostate. The rad oncologist suggest/felt strongly that the pc was probably out of the prostate, but was not detectable. So, I agreed to the pelvic cavity radiation for the first half of 39 days, then ultra-sound guided radiation of the prostate for the remaining days. I chose this method because even after surgery I would have needed(?) pelvic cavity radiation.
So, what about you. Any decision you make must be between you, your partner, & your doctor that will administer the treatment. The point here is that the web will not treat you. The web can help you understand what is happening and what MAY happen after treatment.
I found somewhat helpful, "Report to the Nation on Prostate Cancer, a Guide for Men and Their Families" published by the Prostate Cancer Foundation. It is a big document. The best part is the list of questions that you should ask your doctor, and demand answers. Unfortunately, I did not know about yananow.net until several months after my treatment.
I would also suggest that you talk to someone in Behavioral Health Services. How you chose to deal with pc can be difficult for your brain and your personal relationships.
Have faith & hope, & know that we are all thinking about you, and we are interested in how you make it through this difficult time.
PSA on routine blood testing 65. PSA bounced around between 45 and 65 for five years with no symptoms, including normal DRE.
Yes, five years ... I was in denial and afraid of having the biopsy performed. Yeah, silly but true.
PSA jumped to 115 in 2007. Family/friends persuaded me to have the biopsy. It was positive.
Started hormone therapy to reduce the prostate size and lower the testosterone.
Had every scan known to mankind over the next several months ... all were negative for metastasis.
10/07 had radiation seed implant followed by external beam radiation in 12/07 & 01/08.
PSA in 7/08 was 3.
Now, a year after the radiation treatments ... still on FLOMAX with some burning on urination but those symptoms have improved greatly and some, very little improvement in ED. Feel like I'm doing fine.
Thanks for your reply, it's realy a very similar situation, except I'm trying to deal with it right now, at an early (?) stage. I hope it will make some difference. Allow me to ask a few more questions about your biopsy. What was your Gleason Score ? How many positive samples ? Why haven't you considered surgery ? I'm deeply grateful to you and others who are helping with their experiences.
I too had a high PSA - 182, back in 2005, but MRIs found that bones and lymph nodes were clear.
Now, this is purely my own personal opinion, but I am glad that surgery wasn't an option in my case.
Like others here, I had hormone therapy and radiotherapy, and have come through it all unbelievably well.
I have had no cancer meds at all for 15 months now yet my PSA is stable at around the 1.0 level.
It's been a long journey and I did suffer the usual side effects of treatment, but they have now all disappeared.
The full history is on here on the Mentors pages at:
Whatever decision you make, may I wish you the very best of luck and full recovery.
Hi George, thanks for your attention. I read your story, and noticed that you chose hormone therapy right from the beginning. Why was that ? Why have you rejected surgery ? Was it just based on your high PSA ? I'm very concerned on making such serious decision only based in an inaccurate blood test !!!
I'm sure you have heard it said, but each prostate cancer has a unique set of circumstances. What worked for one person may not for another. There are nomograms online that can help determining if it has escaped the prostate. They told me mine hadn't, but all the nomograms said it had. It had. I had a low PSA, but a Gleason score of 9 (5+4). Not many options. I went with LRP. Now I'm on Hormonal therapy.
Mark ... I absolutely agree and in no way meant to suggest that my choice of treatment was the one for Paul or anyone else. I was merely addressing his request for "similar experiences".
I still don't know if I made the right decision. Unfortunately I had already made the decision prior to joining this forum.
My Urologist and Oncologist were heavily pushing radiation treatment as the likely choice for me and I found no dissent from second and even third opinions so I went with it.
As many of us on here already know and folks like Paul are soon to discover, after the shock of hearing the "C" word we enter the very strange world of "decision making".
The options are seemingly endless and, yes, there are those that have agendas to promote in our decisions. They'll throw facts and figures at us that, quite frankly, we don't understand and promise this or that in side effects and treatment results which may or may not be reliable.
The bottom line is that we must trust someone we feel that has the knowledge to point us in the right direction and that's tuff to do in a life/death situation.
I trust the folks on here and wish I had found this place before making my decision.
Good luck to you Mark and feel free to join us in the "finger crossing" (grin).