Current evidence on the diagnosis and management of immune checkpoint inhibitor associated myocarditis

Immune checkpoint inhibitor-associated myocarditis (ICI-M) is a rare but life-threatening immune-related adverse event. Reported mortality ranges from 27 to 50% in earlier cohorts, with a more recent pooled estimate of approximately 26% in systematic reviews incorporating 2021 to 2022 data. Incidence is approximately 1%, rising to 2 to 4% with combination regimens. We performed a narrative review of the epidemiology, pathophysiology, overlap syndromes, risk stratification, diagnostic criteria, and immunosuppressive management of ICI-M. Diagnosis integrates an obligate rise in high-sensitivity troponin with multimodal imaging, framed by the International Cardio-Oncology Society (IC-OS) 2021 criteria and the 2024 American College of Cardiology (ACC) Consensus Pathway, after exclusion of acute coronary syndrome and infectious myocarditis. Risk stratification is discussed using a recently reported multivariable risk score. High-dose intravenous methylprednisolone is the accepted first-line therapy, with observational data associating higher initial dosing with more favourable biomarkers and survival trends. Up to half of severe cases fail first-line therapy and require escalation. Evidence for second-line agents, including mycophenolate mofetil, tacrolimus, abatacept, anti-thymocyte globulin, infliximab, tocilizumab, and ruxolitinib, derives from case series and small cohorts rather than randomised trials, and is presented with that limitation stated. ICI-M requires a structured, multidisciplinary approach integrating early recognition, systematic risk stratification, prompt high-dose immunosuppression, and a structured escalation approach for steroid-refractory disease, recognising that second-line evidence remains limited. This review synthesises the current, largely observational evidence to support individualised multidisciplinary management, and distinguishes guideline-endorsed recommendations from areas resting on limited or emerging data.

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Publication Details

Journal
Discover Medicine
Published
2026-09-11
DOI
https://doi.org/10.1007/s44337-026-00696-4
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
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article

Current evidence on the diagnosis and management of immune checkpoint inhibitor associated myocarditis

Fahad Farooq, Yasar Ahmed, Hatim Ibrahim, Hebatalla Ismail et al.
Discover Medicine
Cancer Immunotherapy and Biomarkers
article

Current evidence on the diagnosis and management of immune checkpoint inhibitor associated myocarditis

Fahad Farooq, Yasar Ahmed, Hatim Ibrahim, Hebatalla Ismail, Diya M. Sabu
article en

Abstract

Immune checkpoint inhibitor-associated myocarditis (ICI-M) is a rare but life-threatening immune-related adverse event. Reported mortality ranges from 27 to 50% in earlier cohorts, with a more recent pooled estimate of approximately 26% in systematic reviews incorporating 2021 to 2022 data. Incidence is approximately 1%, rising to 2 to 4% with combination regimens. We performed a narrative review of the epidemiology, pathophysiology, overlap syndromes, risk stratification, diagnostic criteria, and immunosuppressive management of ICI-M. Diagnosis integrates an obligate rise in high-sensitivity troponin with multimodal imaging, framed by the International Cardio-Oncology Society (IC-OS) 2021 criteria and the 2024 American College of Cardiology (ACC) Consensus Pathway, after exclusion of acute coronary syndrome and infectious myocarditis. Risk stratification is discussed using a recently reported multivariable risk score. High-dose intravenous methylprednisolone is the accepted first-line therapy, with observational data associating higher initial dosing with more favourable biomarkers and survival trends. Up to half of severe cases fail first-line therapy and require escalation. Evidence for second-line agents, including mycophenolate mofetil, tacrolimus, abatacept, anti-thymocyte globulin, infliximab, tocilizumab, and ruxolitinib, derives from case series and small cohorts rather than randomised trials, and is presented with that limitation stated. ICI-M requires a structured, multidisciplinary approach integrating early recognition, systematic risk stratification, prompt high-dose immunosuppression, and a structured escalation approach for steroid-refractory disease, recognising that second-line evidence remains limited. This review synthesises the current, largely observational evidence to support individualised multidisciplinary management, and distinguishes guideline-endorsed recommendations from areas resting on limited or emerging data.

Discover MedicineVol. 3(1)
University College Dublin (IE), St. Vincent's University Hospital (IE)
Good health and well-being
Openalex Percentile: Top 13%
Cancer Immunotherapy and Biomarkers
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