PSA Trends after Salvage RT and 6 Months of Orgovyx
I completed 6 months of Orgovyx 4 months ago and finished 39 IMRT Salvage radiation treatments 6 months ago. Just had a ultrasensitive PSA test result of .04. I'm told this is a very good result. I am curious as to what PSA trends others have experienced in the first year after completing salvage radiation and 6 months of Orgovyx. Thank you.
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Since .014 is less than < .04 you are in even better shape, another PSA test really isn’t needed with this low a PSA. You are undetectable with either number.
It could be the first lab doesn’t test below .04 while the second one did.
Sorry to hear of your recurrence…but what are your DRS waiting for? Your PSA going from undetectable to .99 and that is an indication that something’s on the move.
I would want to be put on some form of ADT, but first have a PSMA to see if anything lights up. At .99 something must be there, right?
You may only have a small single metastasis which can be successfully treated with SBRT. There have been cases of distant metastases showing up as far away as the clavicle but not present anywhere else. That one particular patient lived for another 14 yrs before he succumbed to something else. Guess we all gotta go from something😁
I had RP in 10/21 and had the usual initial incontinence which gradually improved over the next year. I had gotten to where I didn't need a pad sleeping or at home and could play a round of golf walking and not have any significant leakage in a very light Tena pad.
As part of my treatment for rising PSA in last Q of 2022, I had triple therapy followed by 37 pelvic radiation treatments in April/May 2023. My incontinence has gradually increased since and I have been forced to wear a pad 24/7 and completely soak a light absorbency pad playing golf.
The good news is my PSA has remained undetectable (even with ultra sensitive assay) since my second chemo treatment in Nov 2022. My MO stopped my Darolutamide at the end of my 3 months of chemo and took me off Lupron after one year (last injection was 7/23). My T has failed to return to anywhere near normal levels (52 earlier this month). My MO has referred me to an endocrinologist to begin TRT. He said I am a 90 year old man living in a 70 year old body without T. From his extensive experience (>500 publications on prostate cancer and related topics, 30 years treating this disease, Director of prostate cancer research at Hopkins etc) he believes my aggressive cancer clones have been killed and if my PSA rises on the TRT it can be controlled.
I realize this is a controversial approach. It is not for everyone. It depends on extent of disease, response to treatment, type of treatment, etc etc. I begin my TRT next week and am looking forward to feeling like myself again. The fatigue, muscle loss (despite exercise), diminished libido, depression-all side effects from the very low T, have been difficult to endure. I will be interested to see if my incontinence improves as I continue to do core/kegel exercises and the T helps strengthen these muscles.
Good luck to everyone fighting this beast.