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

There 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 pat...

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Published in:PloS one 2024-12, Vol.19 (12), p.e0314555
Main Authors: Kwan, Jennifer M, Shen, Miles, Akhlaghi, Narjes, Hu, Jiun-Ruey, Mora, Ruben, Cross, James L, Jiang, Matthew, Mankbadi, Michael, Wang, Peter, Zaman, Saif, Lee, Seohyuk, Im, Yunju, Feher, Attila, Liu, Yi-Hwa, Ma, Shuangge S, Tao, Weiwei, Wei, Wei, Baldassarre, Lauren A
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Language:English
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Summary:There 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. We 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. In 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 (P
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0314555