PET/PSMA / Decipher test results back (0.69). Radiation/hormone now.
Well. Was diagnosed with PC back in Oct of last year (53 year old).
My numbers are/were Gleason 7, Stage 2, PSA 8.8, so intermediate risk prostate cancer.
From posting here with my initial diagnosis of PC to now, after researching, weighing my treatment options, and just dealing with the other aspects of life, I finally decided on radiation rather than surgery. So had a PET/PSMA scan a few weeks ago and sample sent in for decipher test. I just got the results of a PSMA/PET scan and Decipher test. While the decipher test is not part of the normal process, I was hoping that results might show a less aggressive type of cancer that might possibly allow me to just have the radiation and forgo the hormone therapy. Unfortunately, even though the PET/PSMA did not show any spread outside the prostate, it is right up against the rectum, and apparently a decipher score of 0.69 is also considered high. So now I will need to start hormone therapy with radiation and possibly some additional drugs for treatment.
It seems that even though my docs advised that I could take my time making a decision on treatment ("Take weeks, months, but not years"), now, based on these latest test results, there seems to be more urgency for treatment. Can't believe it's been over 10 months since my initial diagnosis. Just hoping I didn't take too long to get all these additional tests and decide and put the success of my treatment at risk. I think just an inability to make a decision (surgery vs radiation) and life distracted me.
Interested what others might have to say. Just got off the phone with my doc so just processing the reality of starting treatment as soon as next week and the recent urgency that was conveyed from my oncologist to start treatment.
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TY for your feedback...What is your situation...if I may ask???
I was diagnosed in 2010 Gleason 3+4. Had surgery and they found it to be a 4+3. 3 1/2 years later my PSA started rising, so I had radiation. 2 1/2 years later, I came back again and I started on Lupron. 2 1/2 years later, my PSA started rising, so I was put on Biclutamide. One year later, my PSA started rising and I was put on Zytiga. 2 1/2 years later after a third and serious Afib event my oncologist told me off of Zytiga and put me on Darolutamide. A few months later, I had my one metastasis zapped with SBRT and my PSA has stayrd below .1 for the last 10 months. Just a matter of time before Darolutamide fails and then I can start a PARP inhibitor since I found out I am BRCA2 two years ago and that’s why it keeps coming back.
Now on Orgovyx instead of Lupron, 7+ years with ADT which is so feared by many, not a real problem.
14.5 years now and I really have no side effects from all the drugs, other than some hot flashes and a little brain fog.
I think your on the right course. You're being proactive- thats important . Both methods ( Surgery and Radiation) have similar outcomes from my study , depending on how you go into each setting . One point to ponder on surgery is that you get to do entire pathology on prostate - this is helpful to see exactly what the biology of the prostate is . However , you probably knew this. I had the surgery 3 years ago .... then radiation ( external beam ) 2 years ago at 0.14 PSA . My PSA was rising slowly , so had 22 sessions of radiation. PSA has since gone from 0.14 , then 0.072 , then 0.056 . Next PSA test tomorrow ....hence anxiety . You have this . you seem very well studied ! God Bless . Keep us informed of how your doing Sir . God Bless . James on Vancouver Island .