@ashley2235 , How long has it been since your surgery? How often are they following up with CA19-9, ctDNA, and imaging?
My Whipple surgeon did not recommend a post-op MRI at the 4-week follow-up, as it "would only show the post-op changes in anatomy."
I'm glad the medical oncologist ordered one anyway, because it provided a clean baseline showing no visible cancer at the surgical site or surrounding areas. It helped make the next MRI 3 months later much more evident that the 1.3 cm mass at the original site was a change from prior. That's pretty fast regrowth, but understandable given no adjuvant chemo.
Similarly, CA19-9 had gone down to 12 one month post-op. Several weeks later it was 33 (different lab, part of a follow-up with my PCP). I didn't freak out; it was still below ULN, and I just assumed it was a return to normal levels, maybe related to the different lab, or worst-case, related to some of the post-op dietary adjustment difficulties I was having. It was about 6 weeks from that, at the same point the MRI discovered my 1.3 cm mass, that CA19-9 reached 77.
They did do an immediate EUS biopsy right after that, which came back negative. Since my ctDNA tests were also coming back negative, the tumor board recommended waiting 6 weeks and following up with another MRI. At that point, CA19-9 was 277, the tumor was 2 cm, radiation was not an option, and the surgeon wanted at least 3 months of demonstrated control on chemo before he would reconsider surgery.
When I asked my oncologist if I should restart chemo immediately, he said it was an option, but "didn't think it would change the outcome" (I really wish I had dug deeper into that statement at the time!) and that he didn't recommend treating while there was no definitive evidence of disease.
When I asked if a PET scan could help speed up the diagnosis, I got some long answer that wound up with me not getting a PET scan. I do believe it would have shown FDG uptake and been a tie-breaker vote leading to earlier chemo.
I'm only a "statistical sample of one" but that's the data that guides how I now interpret data and decisions related to my own body, tumor, and their treatment.
I had surgery 6 months ago. I have CT every 3 months, CA19 every month, but do not have ctDNA done. That has never been mentioned. Or rather, my oncologist said it was not covered by insurance. So never discussed again. My CA19 was 12 prior to surgery, 44 upon discharge, and has since been dropping to a level of 16. My oncologist wanted CA19 every 3 months with CT, but I said I want it every month, as it has been a good indicator for me. I return to Mayo on March 18th for CT. I had a lung micronodule at 5 months that I am trying to not worry about, as none of the clinicians seem to be.