My mom is currently on Lonsurf and her cancer is slowly progressing. For example her last CEA climbed from 36 to her recent of 48. My mom was in remission when she first did FOLFOX regimen. Has anyone here did FOLFOX after cancer has metastasized? How was the response? How long were you able to tolerate the neuropathy side effects? Did you take a medication to help with the neuropathy side effect? Any experience and/or recommendations would be helpful. In the meantime, we are still looking for trials but wanting to see if FOLFOX was worth using the second time.
STAGE IV COLONRECTAL CANCER
NON-MSI HIGH
KRAS G12V MUTATATION
MALIGNANCY OF LEFT LUNG AND LYMPH NODES
LAST CEA: 36
CURRENT CEA: 48