{"description":"TEAEs included those from first administration of study treatment up to and including 90 days after last dose of study treatment or up to date of initiation of the first subsequent anticancer therapy (whichever occurred first). Data from the global cohort and China cohort safety analysis sets was summarised separately. 6 patients in the China cohort were also included in the global cohort.","eventGroups":[{"deathsNumAffected":225,"deathsNumAtRisk":266,"description":"During Chemotherapy:\n\nPatients received durvalumab (D) 1500 mg in combination with tremelimumab (T) 75 mg IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9).\n\nPost-Chemotherapy:\n\nPatients then continued to receive durvalumab 1500 mg IV infusion Q4W from Week 12 until PD, unless there was unacceptable toxicity, withdrawal of consent, or another discontinuation criterion was met. Patients also received an additional dose of tremelimumab 75 mg IV infusion post-chemotherapy (in combination with durvalumab) at Week 16 if they completed all 4 doses of durvalumab + tremelimumab during chemotherapy.","id":"EG000","otherNumAffected":249,"otherNumAtRisk":266,"seriousNumAffected":126,"seriousNumAtRisk":266,"title":"Global Cohort: D + T + EP"},{"deathsNumAffected":218,"deathsNumAtRisk":265,"description":"During Chemotherapy:\n\nPatients received durvalumab (D) 1500 mg IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9).\n\nPost-Chemotherapy:\n\nPatients then continued to receive durvalumab 1500 mg IV infusion Q4W from Week 12 until PD, unless there was unacceptable toxicity, withdrawal of consent, or another discontinuation criterion was met.","id":"EG001","otherNumAffected":247,"otherNumAtRisk":265,"seriousNumAffected":86,"seriousNumAtRisk":265,"title":"Global Cohort: D + EP"},{"deathsNumAffected":247,"deathsNumAtRisk":266,"description":"For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). An additional 2 doses of EP (at Weeks 12 and 15) could be given at the investigators' discretion if clinically indicated.","id":"EG002","otherNumAffected":248,"otherNumAtRisk":266,"seriousNumAffected":97,"seriousNumAtRisk":266,"title":"Global Cohort: EP"},{"deathsNumAffected":50,"deathsNumAtRisk":65,"description":"During Chemotherapy:\n\nPatients received durvalumab (D) 1500 mg in combination with tremelimumab (T) 75 mg IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9).\n\nPost-Chemotherapy:\n\nPatients then continued to receive durvalumab 1500 mg IV infusion Q4W from Week 12 until PD, unless there was unacceptable toxicity, withdrawal of consent, or another discontinuation criterion was met. Patients also received an additional dose of tremelimumab 75 mg IV infusion post-chemotherapy (in combination with durvalumab) at Week 16 if they completed all 4 doses of durvalumab + tremelimumab during chemotherapy.","id":"EG003","otherNumAffected":65,"otherNumAtRisk":65,"seriousNumAffected":31,"seriousNumAtRisk":65,"title":"China Cohort: D + T + EP"},{"deathsNumAffected":51,"deathsNumAtRisk":61,"description":"During Chemotherapy:\n\nPatients received durvalumab (D) 1500 mg IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9).\n\nPost-Chemotherapy:\n\nPatients then continued to receive durvalumab 1500 mg IV infusion Q4W from Week 12 until PD, unless there was unacceptable toxicity, withdrawal of consent, or another discontinuation criterion was met.","id":"EG004","otherNumAffected":61,"otherNumAtRisk":61,"seriousNumAffected":26,"seriousNumAtRisk":61,"title":"China Cohort: D + EP"},{"deathsNumAffected":55,"deathsNumAtRisk":62,"description":"For chemotherapy (EP), patients received etoposide (80-100 mg/m\\^2) with either carboplatin (area under the curve 5-6) or cisplatin (75-80 mg/m\\^2) IV infusion Q3W for 4 doses/cycles (Weeks 0, 3, 6 and 9). An additional 2 doses of EP (at Weeks 12 and 15) could be given at the investigators' discretion if clinically indicated.","id":"EG005","otherNumAffected":61,"otherNumAtRisk":62,"seriousNumAffected":22,"seriousNumAtRisk":62,"title":"China Cohort: EP"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 23.0","stats":[{"groupId":"EG000","numAffected":40,"numAtRisk":266,"numEvents":54},{"groupId":"EG001","numAffected":27,"numAtRisk":265,"numEvents":37},{"groupId":"EG002","numAffected":29,"numAtRisk":266,"numEvents":34},{"groupId":"EG003","numAffected":16,"numAtRisk":65,"numEvents":26},{"groupId":"EG004","numAffected":5,"numAtRisk":61,"numEvents":5},{"groupId":"EG005","numAffected":5,"numAtRisk":62,"numEvents":5}],"term":"Diarrhoea"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA 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failure"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 23.0","stats":[{"groupId":"EG000","numAffected":3,"numAtRisk":266,"numEvents":5},{"groupId":"EG001","numAffected":4,"numAtRisk":265,"numEvents":4},{"groupId":"EG002","numAffected":6,"numAtRisk":266,"numEvents":6},{"groupId":"EG003","numAffected":5,"numAtRisk":65,"numEvents":5},{"groupId":"EG004","numAffected":2,"numAtRisk":61,"numEvents":2},{"groupId":"EG005","numAffected":4,"numAtRisk":62,"numEvents":4}],"term":"Leukocytosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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