TY - JOUR
T1 - Cardiovascular magnetic resonance in immune checkpoint inhibitor-Associated myocarditis
AU - Zhang, Lili
AU - Awadalla, Magid
AU - Mahmood, Syed S.
AU - Nohria, Anju
AU - Hassan, Malek Z.O.
AU - Thuny, Franck
AU - Zlotoff, Daniel A.
AU - Murphy, Sean P.
AU - Stone, James R.
AU - Golden, Doll Lauren Alexandra
AU - Alvi, Raza M.
AU - Rokicki, Adam
AU - Jones-O'Connor, Maeve
AU - Cohen, Justine V.
AU - Heinzerling, Lucie M.
AU - Mulligan, Connor
AU - Armanious, Merna
AU - Barac, Ana
AU - Forrestal, Brian J.
AU - Sullivan, Ryan J.
AU - Kwong, Raymond Y.
AU - Yang, Eric H.
AU - Damrongwatanasuk, Rongras
AU - Chen, Carol L.
AU - Gupta, Dipti
AU - Kirchberger, Michael C.
AU - Moslehi, Javid J.
AU - Coelho-Filho, Otavio R.
AU - Ganatra, Sarju
AU - Rizvi, Muhammad A.
AU - Sahni, Gagan
AU - Tocchetti, Carlo G.
AU - Mercurio, Valentina
AU - Mahmoudi, Michael
AU - Lawrence, Donald P.
AU - Reynolds, Kerry L.
AU - Weinsaft, Jonathan W.
AU - Baksi, A. John
AU - Ederhy, Stephane
AU - Groarke, John D.
AU - Lyon, Alexander R.
AU - Fradley, Michael G.
AU - Thavendiranathan, Paaladinesh
AU - Neilan, Tomas G.
N1 - Publisher Copyright:
© 2020 Published on behalf of the European Society of Cardiology. All rights reserved.
PY - 2020/5/7
Y1 - 2020/5/7
N2 - 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.
AB - 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.
KW - Cardiovascular magnetic resonance
KW - Immune checkpoint inhibitor
KW - Myocarditis
UR - http://www.scopus.com/inward/record.url?scp=85084379344&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehaa051
DO - 10.1093/eurheartj/ehaa051
M3 - Article
C2 - 32112560
AN - SCOPUS:85084379344
SN - 0195-668X
VL - 41
SP - 1733
EP - 1743
JO - European Heart Journal
JF - European Heart Journal
IS - 18
ER -