Why is TNBC coming back when doctors said 0.68% chance?

This situation can feel confusing and concerning when personal experience doesn't match the statistics that were shared. Recurrence rates are based on population studies, but individual experiences within support communities can sometimes make rare events feel more common than the overall data suggests. Many others here have navigated similar feelings about statistics versus reality, and this community understands the unique challenges that come with this diagnosis - sharing experiences and questions like this helps everyone process these difficult situations together.

So sorry to hear this is happening to you. I just had bilateral mastectomies after chemo, lumpectomy at which time they found DCIS and pleomorphic LCIS, plus I didn’t get a pCR (I’m RCB2). So took Xeloda for 3 months and more Keytruda, then the mastectomies. Of course the hope is that there is no metastasis, but I know that’s a possibility. What treatment are they recommending for you?