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Nivolumab-AVD versus brentuximab-vedotin-AVD for advanced-stage classical Hodgkin lymphoma in older patients: subgroup analysis of S1826

Dr. Sarah Rutherford
Dr. Sarah Rutherford

The S1826 trial randomized patients with stage III or IV classical Hodgkin lymphoma to six cycles of nivolumab plus AVD (N-AVD) or brentuximab vedotin plus AVD (BV-AVD) and found better progression-free survival in the N-AVD group. Subgroup analysis among patients aged 60 years and older has now been published. Two-year PFS rate was 89% after N-AVD versus 64% after BV-AVD(HR 0.24; 95% CI 0.09-0.63) and two-year OS rate was 96% versus 85% (0.16; 0.03-0.75). Nonrelapse mortality was 6% with N-AVD and 16% with BV-AVD. Neutropenia, febrile neurtopenis, sepsis, infections, and peripheral neuropathy were more frequent with BV-AVD than with N-AVD. The authors conclude that N-AVD is a new standard of care for older patients with advanced-stage cHL fit for anthracycline-based combination therapy.

Original publicationascopubs.org
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