{"description":"All-cause mortality reported for deaths that occurred during study based on ITT, which included all randomized participants. Serious \\& other adverse events reported based on safety population, which included participants who received any amount of any component of study treatment.","eventGroups":[{"deathsNumAffected":11,"deathsNumAtRisk":196,"description":"Participants in the Global population received intravenous infusions of placebo in combination with carboplatin to achieve an initial target AUC of 5 mg/mL/min followed by etoposide 100 mg/m\\^2 on Day 1 of every 21-day cycle during the induction phase (Cycles 1-4). On Days 2 and 3 of every 21-day cycle during the induction phase (Cycles 1-4), etoposide 100 mg/m\\^2 was administered alone. Thereafter, participants received maintenance (Cycle 5 onward) placebo on Day 1 of every 21-day cycle until persistent radiographic PD, symptomatic deterioration, intolerable toxicity, withdrawal of consent, death, or study termination by the Sponsor.","id":"EG000","otherNumAffected":187,"otherNumAtRisk":196,"seriousNumAffected":69,"seriousNumAtRisk":196,"title":"Placebo + Carboplatin + Etoposide - Global"},{"deathsNumAffected":5,"deathsNumAtRisk":198,"description":"Participants in the Global population received intravenous infusions of atezolizumab 1200 milligrams (mg) in combination with carboplatin to achieve an initial target area under the concentration-time curve (AUC) of 5 milligrams per milliliter per minute (mg/mL/min) followed by etoposide 100 milligrams per square meter (mg/m\\^2) on Day 1 of every 21-day cycle during the induction phase (Cycles 1-4). On Days 2 and 3 of every 21-day cycle during the induction phase (Cycles 1-4), etoposide 100 mg/m\\^2 was administered alone. Thereafter, participants received maintenance (Cycle 5 onward) atezolizumab 1200 mg on Day 1 of every 21-day cycle until persistent radiographic PD, symptomatic deterioration, intolerable toxicity, withdrawal of consent, death, or study termination by the Sponsor.","id":"EG001","otherNumAffected":191,"otherNumAtRisk":198,"seriousNumAffected":81,"seriousNumAtRisk":198,"title":"Atezolizumab + Carboplatin + Etoposide - Global"},{"deathsNumAffected":1,"deathsNumAtRisk":52,"description":"Participants in the China population received intravenous infusions of placebo in combination with carboplatin to achieve an initial target AUC of 5 mg/mL/min followed by etoposide 100 mg/m\\^2 on Day 1 of every 21-day cycle during the induction phase (Cycles 1-4). On Days 2 and 3 of every 21-day cycle during the induction phase (Cycles 1-4), etoposide 100 mg/m\\^2 was administered alone. Thereafter, participants received maintenance (Cycle 5 onward) placebo on Day 1 of every 21-day cycle until persistent radiographic PD, symptomatic deterioration, intolerable toxicity, withdrawal of consent, death, or study termination by the Sponsor.","id":"EG002","otherNumAffected":52,"otherNumAtRisk":52,"seriousNumAffected":14,"seriousNumAtRisk":52,"title":"Placebo + Carboplatin + Etoposide - China"},{"deathsNumAffected":3,"deathsNumAtRisk":57,"description":"Participants in the China population received intravenous infusions of atezolizumab 1200 milligrams (mg) in combination with carboplatin to achieve an initial target area under the concentration-time curve (AUC) of 5 milligrams per milliliter per minute (mg/mL/min) followed by etoposide 100 milligrams per square meter (mg/m\\^2) on Day 1 of every 21-day cycle during the induction phase (Cycles 1-4). On Days 2 and 3 of every 21-day cycle during the induction phase (Cycles 1-4), etoposide 100 mg/m\\^2 was administered alone. Thereafter, participants received maintenance (Cycle 5 onward) atezolizumab 1200 mg on Day 1 of every 21-day cycle until persistent radiographic PD, symptomatic deterioration, intolerable toxicity, withdrawal of consent, death, or study termination by the Sponsor.","id":"EG003","otherNumAffected":56,"otherNumAtRisk":57,"seriousNumAffected":22,"seriousNumAtRisk":57,"title":"Atezolizumab + Carboplatin + Etoposide - China"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA version 25.0","stats":[{"groupId":"EG000","numAffected":69,"numAtRisk":196,"numEvents":84},{"groupId":"EG001","numAffected":86,"numAtRisk":198,"numEvents":101},{"groupId":"EG002","numAffected":40,"numAtRisk":52,"numEvents":50},{"groupId":"EG003","numAffected":46,"numAtRisk":57,"numEvents":76}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system 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