The objective of the study was to study the potency of PD-1 inhibitors in patients with NSCLC....Combined results showed that PD-1 inhibitors provided longer OS for EGFR wild-type individuals (HR 0.68; 95% CI, 0.60–0.78; P <0.00001), while did not for EGFR mutant individuals (HR 1.04; 95% CI, 0.70–1.53; P = 0.85) compared with non-PD-1 inhibitor therapy (Figure 3G).