{"description":"Adverse events will be assessed using CTCAE version 5.0. All cause mortality will be reported as all cause mortality within the two year time frame that was analyzed for the primary endpoint.\n\nPlease note that the number of participants at risk for all-cause mortality is greater than the number of participants at risk for adverse events. Only participants who received intervention are eligible for adverse events reporting.","eventGroups":[{"deathsNumAffected":7,"deathsNumAtRisk":487,"description":"Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, dacarbazine IV, and nivolumab IV over 30 minutes on days 1 and 15. Patients may receive pegfilgrastim SC on days 2 and 16, or filgrastim SC or IV on days 6-10 and 21-25. Treatment repeats every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. After completion of cycle 6, patients may receive radiation therapy 5 days per week for approximately 4 weeks at the discretion of the treating physician. Patients also undergo peripheral blood specimen collection and CT, PET/CT and MRI on study.","id":"EG000","otherNumAffected":468,"otherNumAtRisk":481,"seriousNumAffected":140,"seriousNumAtRisk":481,"title":"Arm I (Chemotherapy, Nivolumab, Radiation)"},{"deathsNumAffected":14,"deathsNumAtRisk":483,"description":"Patients receive doxorubicin hydrochloride IV, vinblastine sulfate IV, dacarbazine IV, and brentuximab vedotin IV over 30 minutes on days 1 and 15. Patients may receive pegfilgrastim SC on days 2 and 16, or filgrastim SC or IV on days 6-10 and 21-25. Treatment repeats every 28 days for 6 cycles in the absence of disease progression or unacceptable toxicity. After completion of cycle 6, patients may receive radiation therapy 5 days per week for approximately 4 weeks at the discretion of the treating physician. Patients also undergo peripheral blood specimen collection and CT, PET/CT and MRI on study.","id":"EG001","otherNumAffected":465,"otherNumAtRisk":476,"seriousNumAffected":18,"seriousNumAtRisk":476,"title":"Arm II (Chemotherapy, Brentuximab Vedotin, Radiation)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","stats":[{"groupId":"EG000","numAffected":251,"numAtRisk":481},{"groupId":"EG001","numAffected":252,"numAtRisk":476}],"term":"Anemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","stats":[{"groupId":"EG000","numAffected":23,"numAtRisk":481},{"groupId":"EG001","numAffected":28,"numAtRisk":476}],"term":"Eosinophilia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","stats":[{"groupId":"EG000","numAffected":8,"numAtRisk":481},{"groupId":"EG001","numAffected":30,"numAtRisk":476}],"term":"Febrile 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