4.7 Article

Cardiovascular megnetic resonance in immune checkpoint Inhibitor-associated myocarditis

Journal

EUROPEAN HEART JOURNAL
Volume 41, Issue 18, Pages 1733-+

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehaa051

Keywords

Cardiovascular magnetic resonance; Immune checkpoint inhibitor; Myocarditis

Funding

  1. Sarnoff Cardiovascular Research Foundation
  2. National Institutes of Health (NIH)/National Cancer Institute (NCI) [RO1CA229851, UH2CA207355, RO1CA193970, P30CA008748]
  3. Canadian Institutes of Health Research New Investigator Award [FRN 147814]
  4. Ricerca di Ateneo/Federico II University grant
  5. Kohlberg Foundation
  6. NIH/NHLBI [RO1HL130539, RO1HL137562]
  7. NIH/Harvard Center for AIDS Research [P30 AI060354]

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Aims Myocarditis is a potentially fatal complication of immune checkpoint inhibitors (ICI). Sparse data exist on the use of cardiovascular magnetic resonance (CMR) in ICI-associated myocarditis. In this study, the CMR characteristics and the association between CMR features and cardiovascular events among patients with ICI-associated myocarditis are presented. Methods and results From an international registry of patients with ICI-associated myocarditis, clinical, CMR, and histopathological findings were collected. Major adverse cardiovascular events (MACE) were a composite of cardiovascular death, cardiogenic shock, cardiac arrest, and complete heart block In 103 patients diagnosed with ICI-associated myocarditis who had a CMR, the mean left ventricular ejection fraction (LVEF) was 50%, and 61% of patients had an LVEF >= 50%. Late gadolinium enhancement (LGE) was present in 48% overall, 55% of the reduced EF, and 43% of the preserved EF cohort. Elevated T2-weighted short tau inversion recovery (STIR) was present in 28% overall, 30% of the reduced EF, and 26% of the preserved EF cohort. The presence of LGE increased from 21.6%, when CMR was performed within 4 days of admission to 72.0% when CMR was performed on Day 4 of admission or later. Fifty-six patients had cardiac pathology. Late gadolinium enhancement was present in 35% of patients with pathological fibrosis and elevated T2-weighted STIR signal was present in 26% with a lymphocytic infiltration. Forty-one patients (40%) had MACE over a follow-up time of 5 months. The presence of LGE, LGE pattern, or elevated T2-weighted STIR were not associated with MACE. Conclusion These data suggest caution in reliance on LGE or a qualitative T2-STIR-only approach for the exclusion of ICI-associated myocarditis.

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