Cardiovascular Toxicities of Immune Checkpoint Inhibitors: JACC Review Topic of the Week.

J Am Coll Cardiol

Brigham and Women's Hospital Heart & Vascular Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts. Electronic address:

Published: October 2019

AI Article Synopsis

  • Immune checkpoint inhibitors (ICIs) have significantly improved survival rates in cancer patients, but they can lead to cardiovascular adverse events (CVAEs), particularly myocarditis.
  • Common CVAEs related to ICI use also include pericardial diseases, Takotsubo syndrome, arrhythmias, and vasculitis, which physicians should recognize as serious but rare side effects.
  • Effective management of severe myocarditis typically requires high-dose corticosteroids and stopping ICI treatment, alongside updated guidelines from the National Comprehensive Cancer Network on handling these toxicities.

Article Abstract

Immune checkpoint inhibitors (ICIs) have been an important therapeutic advance in the field of cancer medicine, resulting in a significant improvement in survival of patients with advanced malignancies. Recent reports provided greater insights into the incidence of cardiovascular adverse events (CVAEs) with ICI use. Myocarditis is the most common CVAE associated with ICI. Pericardial diseases, Takotsubo syndrome, arrhythmias, and vasculitis constitute other significant AEs. Physicians should be aware of these infrequent, but potentially fatal toxicities associated with ICIs as their therapeutic use becomes widespread with a myriad of approvals by the U.S. Food and Drug Administration. Management involves prompt administration of high-dose corticosteroids and discontinuation of ICIs in severe myocarditis. This review summarizes the most updated evidence on epidemiology, pathophysiological mechanisms, and management strategies of various CVAEs associated with ICIs. Highlights from recent guidelines published by National Comprehensive Cancer Network on ICI-related CV toxicities have also been incorporated.

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Source
http://dx.doi.org/10.1016/j.jacc.2019.07.079DOI Listing

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