EML4-ALK Mutations in Lung Cancer That Confer Resistance to ALK Inhibitors

Young Lim Choi(Jichi Medical University), Manabu Soda(Jichi Medical University), Yoshihiro Yamashita(Jichi Medical University), Toshihide Ueno(Jichi Medical University), Junpei Takashima(Osaka Prefectural Medical Center), Takahiro Nakajima(Chiba Cancer Center), Yasushi Yatabe(Aichi Cancer Center), Kengo Takeuchi(Japanese Foundation For Cancer Research), Toru Hamada(Jichi Medical University), Hidenori Haruta(Jichi Medical University), Yuichi Ishikawa(Cancer Institute (WIA)), Hideki Kimura(Chiba Cancer Center), Tetsuya Mitsudomi(Aichi Cancer Center), Yoshiro Tanio(Osaka Prefectural Medical Center), Hiroyuki Mano(Jichi Medical University)
New England Journal of Medicine
October 27, 2010
Cited by 1,181Open Access
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Abstract

The EML4 (echinoderm microtubule-associated protein-like 4)-ALK (anaplastic lymphoma kinase) fusion-type tyrosine kinase is an oncoprotein found in 4 to 5% of non-small-cell lung cancers, and clinical trials of specific inhibitors of ALK for the treatment of such tumors are currently under way. Here, we report the discovery of two secondary mutations within the kinase domain of EML4-ALK in tumor cells isolated from a patient during the relapse phase of treatment with an ALK inhibitor. Each mutation developed independently in subclones of the tumor and conferred marked resistance to two different ALK inhibitors. (Funded by the Ministry of Health, Labor, and Welfare of Japan, and others.).


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