As we all know, there are multiple IO-based regimens for the first-line treatment of advanced non-small cell lung cancer. And there’s a lot of clinical equipoise about who may benefit from IO intensification with dual checkpoint blockade. And there’s been a lot of interest in biomarkers that may predict benefit from that intensification, such as KEAP1 or STK11...
As we all know, there are multiple IO-based regimens for the first-line treatment of advanced non-small cell lung cancer. And there’s a lot of clinical equipoise about who may benefit from IO intensification with dual checkpoint blockade. And there’s been a lot of interest in biomarkers that may predict benefit from that intensification, such as KEAP1 or STK11. And so the motivation behind our study was to take a look at whether intensification improves outcomes in real-world populations and specifically in populations with those high-risk alterations in their cancers. So our findings were that, much to our surprise, intensification did not benefit the overall population and did not benefit specifically those patients with high-risk cancers. And so that was a surprise to us because we felt like, you know, we had a good preclinical hypothesis. There’s been a lot of subgroup analyses of the Poseidon trial looking at that. And so I think what it shows us is that there may be a difference between clinical trial populations and the general lung cancer population at large. You know, I don’t think it’s a surprise to say that the general population tends to be sicker, more frail, have more comorbidities. And because of that, is the benefit that folks are getting from dual checkpoint blockade being outweighed by the toxicity that they’re experiencing as well, especially in non-clinical trial populations.
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