In our non-small cell lung cancer cohort, PFS, objective response rate and disease control rate had obvious superiority in the patients with PBRM1 mutation than those without PBRM1 mutation (PFS: HR = .268, 95% CI: 084-.854, p = .04, ORR: 55.56% vs. 20.00%, p = .027, DCR: 100% vs. 75.20%)...the above were fully illustrated the links between the PBRM1 mutation and ICIs response in pan-cancer patients with treated ICIs. PBRM1 mutation be used to a promising immunotherapeutic signature that could guide clinical management and personalized immunotherapy.