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Per protocol, participants receiving switch-over, second course, and switch-over plus second course treatment were monitored for ACM and AEs separately.","eventGroups":[{"deathsNumAffected":225,"deathsNumAtRisk":278,"description":"Participants received pembrolizumab 200 mg by intravenous (IV) infusion prior to chemotherapy on Day 1 of 21-day cycle for up to 35 cycles PLUS Investigator's choice of paclitaxel (200 mg/m\\^2 by IV infusion on Day 1 of each 21-day cycle for 4 cycles) or nab paclitaxel (100 mg/m\\^2 by IV infusion on Days 1, 8, 15 of each 21-day cycle for 4 cycles) PLUS carboplatin Area Under Curve (AUC) 6 by IV infusion on Day 1 of each 21-day cycle for 4 cycles.","id":"EG000","otherNumAffected":270,"otherNumAtRisk":278,"seriousNumAffected":128,"seriousNumAtRisk":278,"title":"Pembrolizumab + Chemotherapy Combo"},{"deathsNumAffected":143,"deathsNumAtRisk":281,"description":"Participants received normal saline as placebo by IV infusion prior to chemotherapy on Day 1 of each 21-day cycle for up to 35 cycles (\\~ 2 years) PLUS Investigator's choice of paclitaxel (200 mg/m\\^2 by IV infusion on Day 1 of each 21-day cycle for 4 cycles) or nab-paclitaxel (100 mg/m\\^2 by IV infusion on Days 1, 8, 15 of each 21-day cycle for 4 cycles) PLUS carboplatin AUC 6 by IV infusion on Day 1 of each 21-day cycle for 4 cycles.","id":"EG001","otherNumAffected":272,"otherNumAtRisk":280,"seriousNumAffected":114,"seriousNumAtRisk":280,"title":"Placebo + Chemotherapy"},{"deathsNumAffected":111,"deathsNumAtRisk":118,"description":"Participants who received saline placebo with chemotherapy and who experienced disease progression, switched over to receive pembrolizumab monotherapy at investigator's discretion. 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