Hi guys. I've been following this community for a little while now and always admired the knowledgeable responses to questions. I've finally reached the point of having PC diagnosed. Will speak to my urologist (surgeon) in a few weeks and also plan to speak with a radiation oncologist. Any advice on what I should ask, and what direction I should be thinking of.
I'm a Gleason 3+4=7, grade group 2. 5% high grade (pattern 4) being 5%. The carcinoma
involves 10%, 10%, 15% and 30% of all cores. There's no cribriform architecture, or apparently any perineural, vascular or extra prostatic infiltration or extension.
I'm not certain if I've got all the info needed, but it's a beginning. I'm living in country Australia.