I’ve got mixed ductal PC. I’m post RALP, post-rad, 6 months into ADT. Setting research about the increased likelihood of metastasis with ductal, and the unreliability of PSA in indicating ductal, I’m anxious to touch all bases before it goes to lungs bones brain or liver. I’m already scheduled for every-6-month PSMA PET scans (although I’ll be asking whether FDG PET is available instead).
I should have the initial genetic consult soon, but I’d like to have a good sense of what’s involved in the process beforehand.
I had an Ancestry test years ago and submitted it to Promethease, which identifies SNPs that may be associated with different traits/diseases. I just checked, and I have quite a few associated with PC. So I’m anticipating confirmation with the MD genetic process.
My main question: we identify specific genetic mutations. What then? Are there medicines or chemo specific to the variations? Are those initiated before evidence of metastasis? Questions I should ask them?