| Literature DB >> 29717400 |
Takuya Oyakawa1, Nao Muraoka2, Kei Iida2, Masatoshi Kusuhara3, Takahisa Kawamura4, Tateaki Naito4, Toshiaki Takahashi4.
Abstract
Crizotinib is a receptor tyrosine kinase inhibitor that has several targets, including c-ros oncogene 1 and the MET proto-oncogene. Considering its known cardiac toxicity, bradycardia is often investigated following treatment with crizotinib. Our patients had bradycardia, QT prolongation, ventricular rhythm, ventricular fibrillation, and pericarditis simultaneously. The cardiotoxicity of crizotinib can sometimes be simultaneous; thus, intensive observation is needed.Entities:
Keywords: Cardiac toxicity; Cardio-oncology; Crizotinib; Lung cancer; MET
Mesh:
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Year: 2018 PMID: 29717400 DOI: 10.1007/s10637-018-0605-x
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850