Cardiac Immune-Related Adverse Events in Immune Checkpoint Inhibition Therapy

Aaron D Brumbaugh1, Roshni Narurkar2, Kaushal Parikh2

  • 1From the Department of Medicine, Allegheny Health Network, Pittsburgh, PA.

Cardiology in Review
|June 19, 2018
PubMed

Insights

Immune checkpoint inhibitors can cause serious cardiovascular side effects like myocarditis. Current guidelines lack clear identification protocols, despite potentially high mortality rates for these immune-related adverse events (irAEs).

Area of Science:

  • Oncology
  • Immunology
  • Cardiology

Background:

  • Immune checkpoint inhibitors (ICIs) are revolutionizing cancer therapy but can trigger immune-related adverse events (irAEs).
  • Cardiovascular irAEs, particularly autoimmune myocarditis, represent a significant clinical challenge.
  • Existing guidelines for anticancer drug cardiovascular effects contrast with the lack of specific protocols for ICI-induced irAEs.

Purpose of the Study:

  • To highlight the spectrum and severity of cardiovascular irAEs associated with immune checkpoint blockade.
  • To underscore the critical need for diagnostic guidelines for ICI-related cardiovascular events.
  • To emphasize the potential underestimation of myocarditis prevalence and the importance of case studies.

Main Methods:

  • Review of existing literature and databases (e.g., WHO database) on ICI-associated cardiovascular irAEs.
  • Analysis of documented cases to understand clinical presentation, outcomes, and potential prevalence.
  • Comparative analysis with guidelines for other cardiotoxic anticancer agents.

Main Results:

  • Autoimmune myocarditis is the most characterized cardiovascular irAE, with reported mortality rates ranging from 36% to 67%.
  • Cardiovascular irAEs can lead to rapid and fatal clinical deterioration.
  • Recent studies suggest autoimmune myocarditis may be more prevalent than previously thought.

Conclusions:

  • There is an urgent need for standardized guidelines for identifying and managing ICI-related cardiovascular irAEs.
  • Improved case identification and understanding are crucial for better patient outcomes.
  • The potential severity and possible underestimation of these events necessitate further research and clinical vigilance.

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