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Published on: February 5, 2020
Risk Factors for Immune Checkpoint Inhibitor-Mediated Cardiovascular Toxicities
Laura I Yousif1, Elles M Screever1, Daniëlle Versluis2
1Department of Cardiology, Thorax Center, Erasmus University Medical Center, P.O. Box 2040, 3000CA, Rotterdam, The Netherlands.
Purpose Of Review:
Immune checkpoint inhibitors (ICIs) have improved the field of cancer, especially in patients with advanced malignancies. Nevertheless, cardiovascular immune-related adverse events (irAEs) with high mortality and morbidity have been observed, including myocarditis, pericarditis, and vasculitis. To date, only a few clinical risk factors have been described and are currently being investigated.
Recent Findings:
In this review, we address the four most prevailing risk factors for cardiovascular irAEs. ICI combination therapy is a predominant risk factor for developing ICI-mediated myocarditis. Additionally, ICI combined with other anti-cancer treatments (e.g., tyrosine kinase inhibitors, radiation, chemotherapy) seems to increase the risk of developing cardiovascular irAEs. Other risk factors include female sex, pre-existing cardiovascular disease, and specific tumors, on which we will further elaborate in this review. An a priori risk strategy to determine who is at risk to develop these cardiovascular irAEs is needed. Insights into the impact of risk factors are therefore warranted to help clinicians improve care and disease management in these patients.
Insights
Immune checkpoint inhibitors (ICIs) can cause severe cardiovascular immune-related adverse events (irAEs). Combination therapies, female sex, pre-existing heart conditions, and certain tumors are key risk factors for these dangerous side effects.
Area of Science:
- Cardiology
- Oncology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment, particularly for advanced malignancies.
- However, cardiovascular immune-related adverse events (irAEs), such as myocarditis, pericarditis, and vasculitis, present significant mortality and morbidity risks.
- Current understanding of clinical risk factors for these events remains limited.
Purpose of the Study:
- To review the predominant risk factors associated with cardiovascular irAEs in patients undergoing ICI therapy.
- To highlight the need for an a priori risk strategy to identify patients at high risk for developing cardiovascular irAEs.
- To provide insights into risk factors to improve clinical care and disease management.
Main Methods:
- Literature review focusing on cardiovascular immune-related adverse events associated with immune checkpoint inhibitors.
- Analysis of identified risk factors including combination therapies, patient demographics, and tumor type.
- Synthesis of current evidence to delineate prevailing risk factors for cardiovascular irAEs.
Main Results:
- ICI combination therapy is a significant risk factor for ICI-mediated myocarditis.
- Concomitant use of ICIs with other anti-cancer treatments (tyrosine kinase inhibitors, radiation, chemotherapy) increases the risk of cardiovascular irAEs.
- Additional risk factors identified include female sex, pre-existing cardiovascular disease, and specific tumor types.
Conclusions:
- Understanding the impact of identified risk factors is crucial for predicting and managing cardiovascular irAEs.
- Developing a proactive risk assessment strategy is essential for patient care.
- Further research into risk stratification will aid clinicians in optimizing treatment and monitoring for cardiovascular complications.
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