Key result
Prompt high-dose immunosuppression is critical for ICI myocarditis given its ~26% mortality.
Why the study?
Immune checkpoint inhibitor-associated myocarditis is a rare but life-threatening adverse event with limited evidence guiding diagnosis and immunosuppressive management.
Population
Patients with immune checkpoint inhibitor-associated myocarditis
Comparison
High-dose intravenous methylprednisolone first-line therapy versus second-line immunosuppressive agents
Design
Narrative review synthesizing observational data and guideline recommendations
Authors
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Supports prompt ICI-M recognition and corticosteroid use per IC-OS criteria; extends pathways but remains hypothesis-generating.
This narrative review synthesizes current observational evidence and guidelines for the multidisciplinary diagnosis, risk stratification, and immunosuppressive management of immune checkpoint inhibitor-associated myocarditis.
Ahmed et al. (2026) conducted a review in Immune checkpoint inhibitor-associated myocarditis. Immunosuppressive therapy (corticosteroids and second-line agents) was evaluated. Immune checkpoint inhibitor-associated myocarditis is a life-threatening complication with approximately 26% mortality, requiring early recognition and prompt high-dose immunosuppression.
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