What we found in FOOTPATH was that if you sequence FOLFOX and FOLFIRI, you retain a good efficacy in terms of progression-free survival, but you also have lower toxicities. So your patients, upon being progressive on the first line regimen, still have reserves in terms of bone marrow reserve or polyneuropathy to go on to other treatment regimens. And also looking into the future, we’re now talking about combining RAS inhibitors and novel agents with frontline chemotherapy...
What we found in FOOTPATH was that if you sequence FOLFOX and FOLFIRI, you retain a good efficacy in terms of progression-free survival, but you also have lower toxicities. So your patients, upon being progressive on the first line regimen, still have reserves in terms of bone marrow reserve or polyneuropathy to go on to other treatment regimens. And also looking into the future, we’re now talking about combining RAS inhibitors and novel agents with frontline chemotherapy. If you’re stacking up multiple agents, chemo plus targeted agents, it might really get a little bit toxic. If you know that you can split at least a chemotherapeutic backbone and top that up with a targeted agent, that could be informative for the future.
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