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Participants received IV infusion of atezolizumab during maintenance treatment phase until loss of clinical benefit.","id":"EG000","otherNumAffected":467,"otherNumAtRisk":473,"seriousNumAffected":252,"seriousNumAtRisk":473,"title":"Arm A (Atezolizumab+Nab-Paclitaxel+Carboplatin)"},{"deathsNumAffected":108,"deathsNumAtRisk":131,"description":"Participants received IV infusion of carboplatin on Day 1 and nab-paclitaxel on Days 1, 8, and 15 of each 21-day cycle for 4 or 6 cycles or until disease progression whichever occurs first during induction treatment phase. Participants received best supportive care during maintenance treatment phase. Switch maintenance to pemetrexed was also permitted. Participants who were consented prior to approval of protocol Version 5 were given the option to cross over to receive atezolizumab as monotherapy until disease progression. This Arm B group includes participants who did not crossover to receive atezolizumab as monotherapy.","id":"EG001","otherNumAffected":127,"otherNumAtRisk":131,"seriousNumAffected":63,"seriousNumAtRisk":131,"title":"Arm B Without Crossover Participants (Nab-Paclitaxel+Carboplatin)"},{"deathsNumAffected":70,"deathsNumAtRisk":101,"description":"Participants received IV infusion of carboplatin on Day 1 and nab-paclitaxel on Days 1, 8, and 15 of each 21-day cycle for 4 or 6 cycles or until disease progression whichever occurs first during induction treatment phase. Participants received best supportive care during maintenance treatment phase. Switch maintenance to pemetrexed was also permitted. Participants who were consented prior to approval of protocol Version 5 were given the option to cross over to receive atezolizumab as monotherapy until disease progression. This Arm B group includes participants who crossed over to receive atezolizumab as monotherapy.","id":"EG002","otherNumAffected":100,"otherNumAtRisk":101,"seriousNumAffected":24,"seriousNumAtRisk":101,"title":"Arm B With Crossover Participants (Nab-Paclitaxel+Carboplatin, After Crossover Atezo Monotherapy)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA version 23.1","stats":[{"groupId":"EG000","numAffected":259,"numAtRisk":473,"numEvents":357},{"groupId":"EG001","numAffected":67,"numAtRisk":131,"numEvents":79},{"groupId":"EG002","numAffected":50,"numAtRisk":101,"numEvents":55}],"term":"ANAEMIA"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA version 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