{"description":"The analysis population is comprised of all treated participants both starting induction and starting maintenance. SAEs are defined per protocol and OAEs represent all remaining adverse events collected (any treatment attribution and any grade) reported on study case report forms. SAEs and OAEs are reported as maximum grade by toxicity type.","eventGroups":[{"deathsNumAffected":0,"deathsNumAtRisk":42,"description":"Lenalidomide (R): 25 mg on days 1-14 orally Subcutaneous Bortezomib (sqV): 1.3 mg/m\\^2 on days 1, 4, 8 and 11 Dexamethasone (d): 20 mg on days 1, 2, 4, 5, 8, 9, 11 and 12 Stem cell mobilization occurs at the end of Cycle 4. Participants may elect to stop treatment at the end of Induction Cycle 4 and proceed to autologous stem cell transplant (ASCT) with melphalan 200 mg/m\\^2 conditioning, or receive a full 8 cycles of RsqVd induction therapy. RsqVd cycle duration is 21-days.","id":"EG000","otherNumAffected":42,"otherNumAtRisk":42,"seriousNumAffected":8,"seriousNumAtRisk":42,"title":"Lenalidomide, Subcutaneous Bortezomib, Dexamethasone - Induction Phase"},{"deathsNumAffected":0,"deathsNumAtRisk":35,"description":"Maintenance follows induction with the specific regimen determined by risk category. High-risk participants defined as those with International Staging System (ISS) stage II or stage III disease and/or high-risk cytogenetics including t(4;14), t(4; 16), del(17p) receive sqV of 1.3 mg/m\\^2 on days 1 and 15 in addition to R 10mg (15mg after cycle 3 if tolerated) on days 1-21 of 28-day cycle. Standard-risk participants receive R monotherapy.","id":"EG001","otherNumAffected":30,"otherNumAtRisk":35,"seriousNumAffected":8,"seriousNumAtRisk":35,"title":"Lenalidomide, [Subcutaneous Bortezomib] - Maintenance Phase"}],"frequencyThreshold":"0","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"CTCAE (4.0)","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":42},{"groupId":"EG001","numAffected":0,"numAtRisk":35}],"term":"Abdominal distension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"CTCAE (4.0)","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":42},{"groupId":"EG001","numAffected":2,"numAtRisk":35}],"term":"Abdominal pain"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Skin and subcutaneous tissue disorders","sourceVocabulary":"CTCAE 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