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Author Spotlight: Investigating HR-Dependent Cardiac Function in Mouse Models Through a Novel Atrial-Pacing Approach
Published on: July 21, 2023
Heart failure in cancer: role of checkpoint inhibitors
Murilo Delgobo1,2, Stefan Frantz1,2
1Department of Internal Medicine I, University Hospital Würzburg, Würzburg, Germany.
Abstract:
The introduction of immune checkpoint inhibitors have greatly improved clinical outcomes in several cancer types, revolutionizing the management of a wide variety of tumors endowed with poor prognosis. Despite its success, high grade immune related adverse events were observed in patients treated with checkpoint inhibitors. While cardiotoxicity was largely underestimated in initial studies, numerous reports of fulminant myocarditis and fatal heart failure (HF) have been recently described. In this review we discuss possible mechanisms involved in cardiac toxicity triggered by inhibition of cytotoxic T lymphocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1) pathway, the most prominent checkpoint inhibitors available in the clinic. Major cardiovascular events associated with checkpoint inhibitors adds another layer of complexity in cancer therapy and urges for an interdisciplinary approach between oncologists, cardiologists, and immunologist.
Insights
Immune checkpoint inhibitors improve cancer outcomes but can cause severe heart problems like myocarditis and heart failure. Understanding these immune-related adverse events is crucial for patient safety.
Area of Science:
- Oncology
- Immunology
- Cardiology
Background:
- Immune checkpoint inhibitors (ICIs) have transformed cancer treatment, improving outcomes for various malignancies.
- Despite efficacy, ICIs are associated with immune-related adverse events (irAEs).
- Cardiac toxicity, including myocarditis and heart failure, is a serious, increasingly recognized irAE.
Purpose of the Study:
- To review the mechanisms underlying cardiac toxicity induced by ICIs.
- To highlight the clinical significance of cardiovascular events associated with ICI therapy.
Main Methods:
- Literature review of studies on ICI-induced cardiotoxicity.
- Discussion of proposed mechanisms involving CTLA-4 and PD-1 pathways.
Main Results:
- ICI therapy can precipitate severe cardiac events, including fulminant myocarditis and fatal heart failure.
- Mechanisms involve immune system activation against cardiac tissues.
Conclusions:
- Cardiotoxicity is a significant concern in ICI therapy, requiring careful monitoring.
- An interdisciplinary approach involving oncologists, cardiologists, and immunologists is essential for managing ICI-induced cardiotoxicity.
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