Dr Buchbinder on Treatment Decisions After Severe irAEs With Nivolumab/Ipilimumab in Melanoma

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Elizabeth Buchbinder, MD, discusses the rationale for investigating nivolumab maintenance therapy in patients with melanoma who experienced severe immune-related adverse effects due to combination therapy with nivolumab and ipilimumab, and details the findings of this investigation.

Elizabeth Buchbinder, MD, assistant professor, Medicine, Harvard Medical School, senior physician, Medical Oncology, Dana-Farber Cancer Institute, discusses the rationale for investigating nivolumab (Opdivo) maintenance therapy in patients with melanoma who experienced severe immune-related adverse effects (irAEs) due to combination therapy with nivolumab and ipilimumab (Yervoy), and details the findings of this investigation.

Many patients with metastatic melanoma who are treated with the combination of ipilimumab and nivolumab in the frontline develop toxicity following only a few doses, Buchbinder begins. Typically, this means that treatment is stopped, and the patient will then receive steroids or another immunosuppressive therapy, followed by the decision of whether to resume immunotherapy, she says. Notably, these patients will have residual disease on the scan, Buchbinder explains.

To combat this difficult decision, some patients in this situation will be treated with nivolumab alone, Buchbinder expands. Many of the irAEs could stem from the combination of these therapies, leading to the decision to treat with nivolumab alone. However, some clinicians will opt for observation until patients experience disease progression before deciding on another treatment, Buchbinder says. Based on these varying practice patterns, investigators further examine each approach, Buchbinder emphasizes.

A retrospective analysis presented at the 2023 ASCO Annual Meeting found differences in practice that weren't based on patient factors; rather, they were based on physician factors, Buchbinder continues. Findings showed that patients who resumed nivolumab monotherapy (n = 46) experienced a 68% reduction in the risk of death compared with those who did not resume nivolumab (n = 76; HR, 0.32; 95% CI, 0.12-0.84). Among patients who resumed treatment, 26% (n = 12) experienced any-grade irAEs, and 5 patients had grade 3 irAEs. No grade 4 or 5 irAEs were reported.

Given the rates of irAEs and improved survival for patients who resumed maintenance nivolumab, these data suggest that giving more immunotherapy following the resolution of initial severe irAEs could be beneficial and should be prospectively studied, she concludes.

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