Immune checkpoint inhibitors and cardiotoxicity: possible mechanisms, manifestations, diagnosis and management

Expert Rev Anticancer Ther. 2021 Nov;21(11):1211-1228. doi: 10.1080/14737140.2021.1979396. Epub 2021 Sep 21.

Abstract

Introduction: Immune checkpoint inhibitors (ICIs) are a new class of anticancer drugs that enhance the immune system function and activate T cells against cancerous cells. Although cardiac complications are not common, they could be accompanied with high morbidity and mortality.

Areas covered: Regarding the importance of cardiac complications and their subsequent burden on individuals and the healthcare system, this review attempts to discuss the mechanism, diagnosis, and management of myocarditis, besides recapitulating the possible mechanism of other cardiac adverse events. Moreover, we briefly discuss the concurrent administration of other chemotherapeutic agents.

Expert opinion: Due to insufficient knowledge concerning the physiopathology of immune-related adverse events (irAEs) and their potential further complications, cardiovascular complications in particular and in the context of this paper's focus, cooperation of oncologists, immunologists, and cardiologists is necessary for the management of patients. Experimental approaches such as using corticosteroids are becoming a part of guidelines for managing cardiac irAEs. However, a unique algorithm for diagnosis and management is necessary, especially in myocarditis cases. Furthermore, more studies are required to resolve current challenges, including prevention of myocarditis, concurrent administration of other chemotherapeutic agents, and re-introducing patients with ICIs.

Keywords: Immune checkpoint inhibitors; adverse events; cancer; cardiotoxicity; complication.

Publication types

  • Review

MeSH terms

  • Cardiotoxicity / diagnosis
  • Cardiotoxicity / etiology
  • Humans
  • Immune Checkpoint Inhibitors / adverse effects
  • Myocarditis* / chemically induced
  • Myocarditis* / diagnosis
  • Myocarditis* / therapy
  • Neoplasms*

Substances

  • Immune Checkpoint Inhibitors