Key result
ICI myocarditis carries ~46% mortality, demanding rapid diagnosis and multidisciplinary management.
Why the study?
Immune checkpoint inhibitor-related myocarditis carries a mortality rate reaching 46%, necessitating rapid diagnosis and a multidisciplinary management approach.
This review highlights the critical need for rapid diagnosis and multidisciplinary management of ICI-associated myocarditis due to its high mortality rate of up to 46%.
Demands vigilance for cardiac symptoms during ICI therapy; leaves open optimal diagnostic and management protocols pending prospective data.
Immune checkpoint inhibitors (ICI) have caused radical changes in the treatment scheme of many types of cancer in the past 10 years. ICIs are specific monoclonal antibodies that increase T-cell mediated immune response against cancer cells. Despite important advances in cancer treatment, uncontrolled activation of cytotoxic T cells has brought along many autoimmune clinical side effects, especially acute myocarditis. Although the incidence of ICI-related myocarditis is about 1%, it is remarkable in terms of mortality rate reaching 46% and demonstrating the necessity of rapid diagnosis and multidisciplinary approach. The present review aimed to summarize the heterogeneous symptomatology of ICI-associated myocarditis, clinical presentation ranging from elevated asymptomatic cardiac enzyme levels to cardiogenic shock, prominent diagnostic value of cardiac magnetic resonance imaging, and current information on the effectiveness of immunosuppressants in therapy.
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Muhammet Gürdoğan (2020) conducted a review in Immune checkpoint inhibitor-associated myocarditis. Immune checkpoint inhibitors was evaluated. Immune checkpoint inhibitor-related myocarditis has an incidence of approximately 1% but carries a high mortality rate reaching 46%, necessitating rapid diagnosis and a multidisciplinary approach.
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