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Multicenter Study
. 2018 Apr 24;71(16):1755-1764.
doi: 10.1016/j.jacc.2018.02.037. Epub 2018 Mar 19.

Myocarditis in Patients Treated With Immune Checkpoint Inhibitors

Syed S Mahmood  1 , Michael G Fradley  2 , Justine V Cohen  3 , Anju Nohria  4 , Kerry L Reynolds  3 , Lucie M Heinzerling  5 , Ryan J Sullivan  3 , Rongras Damrongwatanasuk  2 , Carol L Chen  6 , Dipti Gupta  6 , Michael C Kirchberger  5 , Magid Awadalla  7 , Malek Z O Hassan  7 , Javid J Moslehi  8 , Sachin P Shah  9 , Sarju Ganatra  9 , Paaladinesh Thavendiranathan  10 , Donald P Lawrence  3 , John D Groarke  4 , Tomas G Neilan  11
Affiliations
Multicenter Study

Myocarditis in Patients Treated With Immune Checkpoint Inhibitors

Syed S Mahmood et al. J Am Coll Cardiol. .

Abstract

Background: Myocarditis is an uncommon, but potentially fatal, toxicity of immune checkpoint inhibitors (ICI). Myocarditis after ICI has not been well characterized.

Objectives: The authors sought to understand the presentation and clinical course of ICI-associated myocarditis.

Methods: After observation of sporadic ICI-associated myocarditis cases, the authors created a multicenter registry with 8 sites. From November 2013 to July 2017, there were 35 patients with ICI-associated myocarditis, who were compared to a random sample of 105 ICI-treated patients without myocarditis. Covariates of interest were extracted from medical records including the occurrence of major adverse cardiac events (MACE), defined as the composite of cardiovascular death, cardiogenic shock, cardiac arrest, and hemodynamically significant complete heart block.

Results: The prevalence of myocarditis was 1.14% with a median time of onset of 34 days after starting ICI (interquartile range: 21 to 75 days). Cases were 65 ± 13 years of age, 29% were female, and 54% had no other immune-related side effects. Relative to controls, combination ICI (34% vs. 2%; p < 0.001) and diabetes (34% vs. 13%; p = 0.01) were more common in cases. Over 102 days (interquartile range: 62 to 214 days) of median follow-up, 16 (46%) developed MACE; 38% of MACE occurred with normal ejection fraction. There was a 4-fold increased risk of MACE with troponin T of ≥1.5 ng/ml (hazard ratio: 4.0; 95% confidence interval: 1.5 to 10.9; p = 0.003). Steroids were administered in 89%, and lower steroids doses were associated with higher residual troponin and higher MACE rates.

Conclusions: Myocarditis after ICI therapy may be more common than appreciated, occurs early after starting treatment, has a malignant course, and responds to higher steroid doses.

Keywords: cardio-oncology; checkpoint inhibitor; ipilimumab; myocarditis; nivolumab; pembrolizumab.

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Figures

FIGURE 1
FIGURE 1. Clinical Presentation of Patients With ICI-Associated Myocarditis
Time from ICI to onset of clinical myocarditis in each of the 35 cases of myocarditis (A). The ICI was administered on day 0. A description of the results for the ECG (B), troponin (C), LVEF (D), and natriuretic peptides (E), standard tests performed at the time of presentation with myocarditis, in patients with myocarditis related to ICI. ECG = electrocardiography; ICI = immune checkpoint inhibitors; LVEF = left ventricular ejection fraction; NT-proBNP = N-terminal pro–B-type natriuretic peptide.
CENTRAL ILLUSTRATION
CENTRAL ILLUSTRATION. Algorithm for Work-Up and Management of Immune-Mediated Myocarditis
Algorithm based on study findings, and institutional experience with 35 cases of ICI-associated myocarditis. CVD = cardiovascular; ECG = electrocardiogram; ICI = immune checkpoint inhibitors.
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