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Treatment repeats every 21 days for 5 cycles in the absence of disease progression or unacceptable toxicity.","id":"EG000","otherNumAffected":206,"otherNumAtRisk":287,"seriousNumAffected":11,"seriousNumAtRisk":287,"title":"Arm I (ABVE-PC)"},{"deathsNumAffected":2,"deathsNumAtRisk":298,"description":"Patients receive brentuximab vedotin IV on day 1. Patients also receive doxorubicin hydrochloride, etoposide, prednisone or methylprednisolone, and cyclophosphamide as in Arm I and vincristine sulfate IV on day 8. 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Ineligible patients are excluded. 5 patients (Arm I: 2 patients; Arm II: 3 patients) were also excluded from adverse events reporting due to never receiving any treatment, but their mortality status was observed. All-Cause Mortality includes all deaths collected on the study."}