
Nicolas Girard, MD, on the Rationale and Design of the Phase 3 CheckMate 816 Trial in Resectable NSCLC
In an interview with CancerNetwork®, Nicolas Girard, MD, discussed the rationale for assessing nivolumab and chemotherapy in resectable non–small cell lung cancer and the design of the phase 3 CheckMate 816 trial.
In an interview with CancerNetwork® during the
In addition to highlighting previous findings with the combination, he detailed the design of the phase 3 CheckMate 816 trial (NCT02998528), which assessed the regimen vs chemotherapy alone in the aforementioned patient population.
Transcript:
We have many phase 2 studies that demonstrated the benefit of neoadjuvant immunotherapy with immune checkpoint inhibitors targeting PD-1 or PD-L1, especially in terms of pathological response. [As these were] only phase 2 studies, it has always been difficult to know whether this is a true benefit compared with the standard of care, which historically has been chemotherapy. In this study, Checkmate 816, we randomized 358 patients to a combination of nivolumab plus chemotherapy vs chemotherapy alone.
[The trial had] 2 primary end points [including] pathological complete response and event-free survival. The advantage of the neoadjuvant approach is to include all the patients eligible for surgical resection of the tumor. With that, we treated the patients for 3 cycles before surgery and then surgery was performed in the majority of patients—83.2% in the experimental [arm] and 75.4% in the control [arm].
Reference
Forde PM, Spicer J, Lu S, et al. CheckMate 816 Investigators. Neoadjuvant nivolumab plus chemotherapy in resectable lung cancer. N Engl J Med. Published online April 11, 2022. doi:10.1056/NEJMoa2202170
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