| Literature DB >> 28781805 |
Yuto Yasuda1, Yasuyo Nishikawa2, Yuichi Sakamori1, Makoto Terao3, Kentaro Hashimoto4, Tomoko Funazo1, Takashi Nomizo1, Takahiro Tsuji1, Hironori Yoshida1, Hiroki Nagai1, Hiroaki Ozasa1, Toyohiro Hirai1, Young Hak Kim1.
Abstract
Crizotinib is one of the molecularly-targeted agents targeted against anaplastic lymphoma kinase (ALK)-rearranged non-small-cell lung cancer (NSCLC). Although its effects appear to be promising, crizotinib may cause adverse effects in patients with ALK-rearranged NSCLC. Hepatic laboratory abnormalities are frequently observed with crizotinib and treatment discontinuation is occasionally required. We herein report the case of a 51-year-old woman diagnosed with relapsed ALK-rearranged NSCLC, who received crizotinib as second-line systemic chemotherapy. After 17 days of crizotinib therapy, the patient developed grade >3 hepatotoxicity. Treatment discontinuation improved the laboratory abnormalities and fifth-line oral desensitization with crizotinib achieved successful response without hepatotoxicity. Therefore, oral desensitization with crizotinib may be a viable option following crizotinib-induced hepatitis.Entities:
Keywords: anaplastic lymphoma kinase; crizotinib; desensitization; hepatitis; non-small-cell lung cancer
Year: 2017 PMID: 28781805 PMCID: PMC5532690 DOI: 10.3892/mco.2017.1310
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450