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Mark Yarchoan, MD

Articles by Mark Yarchoan, MD

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Panelists discuss how immune-related adverse events typically occur between 3 and 15 weeks of treatment, with hepatitis being particularly concerning in patients with cirrhosis and requiring careful differentiation from disease progression or worsening cirrhosis, while high-dose steroids remain first-line treatment with consideration of steroid-sparing agents and potential rechallenge strategies for responding patients.

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Panelists discuss how dual checkpoint inhibitors demonstrate significantly higher immune-related adverse event rates (nearly 30% grade 3-4) compared with atezolizumab-bevacizumab, but this increased toxicity is accompanied by meaningfully improved response rates, and the addition of anti-CTLA4 therapy roughly doubles response rates compared with anti-PD1 monotherapy in HCC.

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Panelists discuss how all 3 approved immunotherapy doublets (atezolizumab-bevacizumab, durvalumab-tremelimumab, and nivolumab-ipilimumab) demonstrate superiority over tyrosine kinase inhibitor therapy, with each regimen offering distinct advantages—atezolizumab-bevacizumab for disease control, and dual checkpoint inhibitors for durable complete responses and long-term survival tails.

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