Early evaluation of severe immune checkpoint inhibitor-associated myocarditis: a real-world clinical practice
Xin Tang1, Yuan Li1, He Huang2
1Department of Radiology, Functional and Molecular Imaging Key Laboratory of Sichuan Province, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Insights
Predictors for severe immune checkpoint inhibitor (ICI)-associated myocarditis were identified. Prior chemotherapy and higher neutrophil ratios indicated poorer outcomes, while lymphocyte and CD4+ T cell ratios suggested better cardiac outcomes in ICI-treated patients.
Area of Science:
- Cardiology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) are crucial in cancer therapy but can cause severe myocarditis.
- Early identification of severe ICI-associated myocarditis is critical for patient management.
Purpose of the Study:
- To investigate clinical features and examination results that predict the severity of immune checkpoint inhibitor (ICI)-associated myocarditis.
- To identify prognostic markers for severe ICI-induced myocarditis.
Main Methods:
- Retrospective analysis of 81 cancer patients with ICI-associated myocarditis.
- Endpoints included Common Terminology Criteria for Adverse Events (CTCAE) grades 3-5 and major adverse cardiovascular events (MACE).
- Logistic regression analyzed predictive values of clinical and laboratory factors.
Main Results:
- Over half of patients (53.1%) experienced CTCAE grades 3-5 myocarditis; 34.6% had MACE.
- Severity correlated with affected organs, initial symptoms, and prior chemotherapy.
- Higher neutrophil ratios predicted poorer outcomes; lymphocyte, monocyte, CD4+ T cell, and CD4/CD8 ratios predicted better outcomes.
- Cardiovascular magnetic resonance showed predictive value, while echocardiography and ECG had limited utility.
Conclusions:
- Clinical characteristics and specific immune cell ratios predict ICI-associated myocarditis severity.
- Identifying these predictors aids in early detection and management of severe ICI-induced myocarditis.
Purpose:
Immune checkpoint inhibitor (ICI)-associated myocarditis is a rare but severe complication for patients treated with immunotherapy. This study aims to explore the predictive significance of patients' clinical features and examination results for the severity of ICI-associated myocarditis.
Methods:
Data from a real-world cohort of 81 cancer patients who developed ICI-associated myocarditis after immunotherapy were retrospectively analyzed. The development of myocarditis of Common Terminology Criteria for Adverse Events (CTCAE) grades 3-5 and/or the major adverse cardiovascular event (MACE) was set as endpoints. Logistic regression was used to evaluate the predictive value of each factor.
Results:
CTCAE grades 3-5 and MACE developed in 43/81 (53.1%) and 28/81 (34.6%) cases, respectively. The likelihood of CTCAE grades 3-5 and MACE increased with the accumulation of organs affected by the ICI-associated adverse events and initial clinical symptoms. Concurrent systematic therapies during ICI treatment did not raise the risk of myocarditis severity, while prior chemotherapy did. Besides classical serum cardiac markers, a higher neutrophil ratio was also related to poorer cardiac outcomes, whereas higher lymphocyte and monocyte ratios were predictors of favorable cardiac outcomes. The CD4+ T cell ratio and CD4/CD8 ratio were negatively related to CTCAE grades 3-5. Several cardiovascular magnetic resonance parameters were associated with myocarditis severity, whereas the predictive value of echocardiography and electrocardiogram was weak.
Conclusion:
This study comprehensively evaluated the prognostic value of patients' clinical characteristics and examination results and identified several predictors of severe ICI-associated myocarditis, which will facilitate early detection of severe ICI-associated myocarditis in patients receiving immunotherapy.
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