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. 2022 Jul;11(7):1247–1267. doi: 10.21037/tlcr-22-527

Table 6. Postoperative adjuvant immunotherapy for NSCLC.

Trial Eligible patients Intervention following surgery Estimated enrolment (N) Primary endpoint Median follow-up HR
IMpower 010 IB–IIIA
NSCLC
Arm A: platinum doublet (4 cycles) followed by atezo (16 cycles).
Arm B: platinum doublet (4 cycles) followed by best supportive care
1,280 DFS 32.8 m 0.66 (95% CI: 0.50–0.88) in PD-L1 + II–IIIA patients
PEARLS/KEYNOTE-091 IB–IIIA
NSCLC
Arm A: (optional chemotherapy) pembro (1 year).
Arm B: (optional chemotherapy) placebo (1 year)
1,080 DFS 35.6 m 0.76 (95% CI: 0.63–0.91) in ITT patients. 0.82 (95% CI: 0.57–1.18) in PD-L1 TPS ≥50% patients
ANVIL IB–IIIA
NSCLC
Arm A: (optional chemotherapy and RT) nivolumab (1 year).
Arm B: (optional chemotherapy and RT) observation
903 DFS/OS NG NG
BR31 IB–IIIA
NSCLC
Arm A: (optional chemotherapy and RT if N2) duva (1 year).
Arm B: (optional chemotherapy and RT if N2) placebo (1 year)
1,360 DFS NG NG
ALCHEMIST IB–IIIA
NSCLC
Arm A: platinum doublet (4 cycles).
Arm B: platinum doublet (4 cycles)
followed by pembrolizumab (17 cycles).
Arm C: platinum doublet plus pembrolizumab (4 cycles)
followed by pembrolizumab (additional 13 cycles)
1,263 DFS/OS NG NG

NSCLC, non-small cell lung cancer; atezo, atezolizumab; pembro, pembrolizumab; duva, durvalumab; DFS, disease-free survival; OS, overall survival; NG, not given; ITT, intention-to-treat; TPS, tumor proportion score; PD-L1, programmed cell death-ligand 1.