{"description":"All-cause mortality was collected for all participants enrolled/randomized in the study and is presented according to the randomized treatment arm. Serious AEs and other AEs were collected for all participants in the safety population who received at least one dose of study drug. Participants in the safety population were analyzed according to the treatment arm corresponding to the actual treatment received.","eventGroups":[{"deathsNumAffected":22,"deathsNumAtRisk":226,"description":"Carfilzomib was administered twice-weekly intravenously as a 10 ± 5 minute infusion using an infusion pump on Days 1, 2, 8, 9, 15, and 16 of each 28-day cycle. The dose was 20 mg/m\\^2 on Days 1 and 2 of Cycle 1 and 27 mg/m\\^2 beginning on Day 8 of Cycle 1 and thereafter. Participants also received lenalidomide 25 mg daily orally on Days 1 to 21 of each cycle and dexamethasone 40 mg weekly orally or intravenously. Participants were treated for up to 12 28-day cycles.","id":"EG000","otherNumAffected":190,"otherNumAtRisk":231,"seriousNumAffected":75,"seriousNumAtRisk":231,"title":"Twice-weekly KRd 20/27 mg/m^2"},{"deathsNumAffected":26,"deathsNumAtRisk":228,"description":"Carfilzomib was administered once-weekly intravenously as a 30 ± 5 minute infusion using an infusion pump on Days 1, 8, and 15 of each 28-day cycle. The dose was 20 mg/m\\^2 on Day 1 of Cycle 1 and 56 mg/m\\^2 beginning on Day 8 of Cycle 1 and thereafter. Participants also received lenalidomide 25 mg daily orally on Days 1 to 21 of each cycle and dexamethasone 40 mg weekly orally or intravenously. Participants were treated for up to 12 28-day cycles.","id":"EG001","otherNumAffected":182,"otherNumAtRisk":223,"seriousNumAffected":84,"seriousNumAtRisk":223,"title":"Once-weekly KRd 20/56 mg/m^2"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 26.0","stats":[{"groupId":"EG000","numAffected":55,"numAtRisk":231},{"groupId":"EG001","numAffected":56,"numAtRisk":223}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 26.0","stats":[{"groupId":"EG000","numAffected":73,"numAtRisk":231},{"groupId":"EG001","numAffected":65,"numAtRisk":223}],"term":"Neutropenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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AEs were collected from first dose of study drug to last dose of study drug + 30 days; median treatment duration (any study treatment) was 11.8 months."}