We have had Foundation One test and Gradient Blood biopsy which both report CDK12 mutation.
There is no “definitive” SOC for this rare mutation.
We are in yr 5 since RP surgery, radiation, and two rounds of Lupron/Casodex.
The Lupron/Casodex has stopped working. PSA went from .9 to 2.9 in 6 months.
He had a PSMA scan two weeks ago … and it came back as “clear” of any activity. No change since PSMA scan in September of 2020.
With his PSA being 2.9 I would think something would have shown up on PSMA scan.
Dr. Antonarakas is suggesting Nebuqa (sp?) with Casodex as next line of treatment.
Any thoughts?
Thank you!