I love Roy's response... spot on. I'm certainly no oncologist or doctor of any kind, but I've been counseling hundreds of EC patients around the world for over 3 years. I'm only 4 1/2 years since dx, and just over 4 years post-op. I've had Signatera testing done every 3 months since Oct 2020.
I admit I'm puzzled when I see others reporting Signatera results while they are stage 4 and undergoing treatments. There's zero doubt your cancer is out and about and will certainly be seen in your bloodstream. But the relativeness of these numbers... I'm a bit suspect of. For many of us, Natera testing is started post-op, when it is believed we've reached NED status from all our chemoradiation treatments and subsequent esophagectomies. Are we truly NED at a month or two post-op... who the hell knows... and even our many doctors can not be sure. And if they tell you that you are now cancer free... They're full of sht... and irresponsible.
But... it's a good starting point, and if a zero baseline is achieved, future Signatera testing will be a good relative indicator of what's floating around in the bloodstream (ctDNA). But this is not the Be All End All... just another tool to monitor us like our scans and endoscopies and symptoms we are feeling. But again... I'm not sure just significance there is from running Signatera tests on active stage 4s receiving chemo treatments.
We do see protein monitoring in general... for CA 19-9, CEA, CA 125, etc. But even these numbers jumping around... can be a bit misleading. But Signatera testing... looking for YOUR cancer's signature in YOUR bloodstream, is different. All the best.
Gary
@mrgvw Thank you for your comments. I was dx stage 4 appendix cancer in 2021. I started fortnightly CEA protein blood tests before my fortnightly Folfiri + Avastin infusions. I chose to leave Folfox to plan B if needed.
I asked my oncologist not to tell me my results, unless we needed to worry and look at Folfox. I didn’t want the stress if I didn’t need it. Only once was he concerned and said we may need to change after my next results. Next infusion he said any concerns had gone and it was business as usual. I have no idea what my numbers ever were. My choice.
After a year of various treatments including 2 major surgeries I was finally NED in 2022 . I chose to stop treatment then. I haven’t been treated since. My oncologist says my gamble worked for me and now we only attack if/when the cancer comes back on my tests. I am periodically scanned (3 monthly now 4 monthly) PET-CT and CEA etc blood tests and meet my oncologist to hear his take on the results.
I have never had Signatera but have read about it. Our Medicare system in Australia doesn’t cover it. In a way I’m glad I haven’t. This stress seems awful.
I hope everyone who is worrying about their Signatera numbers fights on if needed 🙏🙏 That’s my plan if my tests show anything that concerns my oncologist 🙏🙏