PLoS ONE (Jan 2024)

Adverse cardiovascular events and cardiac imaging findings in patients on immune checkpoint inhibitors.

  • Jennifer M Kwan,
  • Miles Shen,
  • Narjes Akhlaghi,
  • Jiun-Ruey Hu,
  • Ruben Mora,
  • James L Cross,
  • Matthew Jiang,
  • Michael Mankbadi,
  • Peter Wang,
  • Saif Zaman,
  • Seohyuk Lee,
  • Yunju Im,
  • Attila Feher,
  • Yi-Hwa Liu,
  • Shuangge S Ma,
  • Weiwei Tao,
  • Wei Wei,
  • Lauren A Baldassarre

DOI
https://doi.org/10.1371/journal.pone.0314555
Journal volume & issue
Vol. 19, no. 12
p. e0314555

Abstract

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BackgroundThere is an urgent need to better understand the diverse presentations, risk factors, and outcomes of immune checkpoint inhibitor (ICI)-associated cardiovascular toxicity. There remains a lack of consensus surrounding cardiovascular screening, risk stratification, and clinical decision-making in patients receiving ICIs.MethodsWe conducted a single center retrospective cohort study including 2165 cancer patients treated with ICIs between 2013 and 2020. The primary outcome was adverse cardiovascular events (ACE): a composite of myocardial infarction, coronary artery disease, stroke, peripheral vascular disease, arrhythmias, heart failure, valvular disease, pericardial disease, and myocarditis. Secondary outcomes included all-cause mortality and the individual components of ACE. We additionally conducted an imaging substudy examining imaging characteristics from echocardiography (echo) and cardiac magnetic resonance (CMR) imaging.ResultsIn our cohort, 44% (n = 962/2165) of patients experienced ACE. In a multivariable analysis, dual ICI therapy (hazard ratio [HR] 1.23, confidence interval [CI] 1.04-1.45), age (HR 1.01, CI 1.00-1.01), male sex (HR 1.18, CI 1.02-1.36), prior arrhythmia (HR 1.22, CI 1.03-1.43), lung cancer (HR 1.17, CI 1.01-1.37), and central nervous system (CNS) malignancy (HR 1.23, CI 1.02-1.47), were independently associated with increased ACE. ACE was independently associated with a 2.7-fold increased risk of mortality (PConclusionDual ICI therapy, prior arrhythmia, older age, lung and CNS malignancies were independently associated with an increased risk of ACE, and dual ICI therapy was also independently associated with an increased risk of myo/pericarditis, highlighting the utmost importance of cardiovascular risk factor optimization in this particularly high-risk population. Fortunately, the occurrence of myo/pericarditis was relatively uncommon, and the overall cardiovascular risks of dual ICI therapy appeared to be offset by a significant mortality benefit. The use of multimodal cardiac imaging can be helpful in stratifying risk and guiding preventative cardiovascular management in patients receiving ICIs.