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Updated: Jun 14, 2026

Isolation and Identification of Extravascular Immune Cells of the Heart
Published on: August 23, 2018
Predictors of Immune-Related Cardiac Adverse Events in Patients Receiving Immune Checkpoint Inhibitors: A
Ileana-Raluca Pătru1,2, Andreea-Iuliana Ionescu1,2,3, Alina Gabriela Negru4
1Medical Oncology Department, Colțea Clinical Hospital, 030167 Bucharest, Romania.
None:
Background/Objectives: Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events (irAEs), including cardiac toxicities, which may have significant clinical impact. Data regarding predictors of immune-mediated cardiac toxicity remain limited. The aim of this study was to evaluate the association between cardiovascular comorbidities and the development of cardiac irAEs, as well as to assess their potential role in predicting non-cardiac irAEs. Methods: We conducted a retrospective observational study including oncological patients treated with immune checkpoint inhibitors at Colțea Clinical Hospital. Patients with complete clinical data and documented cardiac and non-cardiac irAEs were included. Demographic characteristics, prior oncological treatments, cardiovascular comorbidities, and relevant clinical parameters were analyzed. Univariate and multivariate logistic regression analyses were performed to identify predictors of immune-related adverse events. Results: Hypercholesterolemia, atrial fibrillation, history of acute coronary syndrome, and heart failure were significantly associated with the development of cardiac irAEs. In multivariate analysis, hypercholesterolemia and pre-existing cardiovascular disease remained independent predictors of cardiac toxicity. No significant association was observed between non-cardiac irAEs and cardiac irAEs. The predictive model demonstrated high specificity but moderate sensitivity. Conclusions: Cardiovascular comorbidities play a significant role in the development of immune-related cardiac toxicities. Identification of these risk factors may improve patient stratification and support individualized monitoring strategies in patients receiving immune checkpoint inhibitors.
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