| Literature DB >> 23787064 |
Gouji Toyokawa1, Mitsuhiro Takenoyama2, Kenichi Taguchi3, Ryo Toyozawa1, Eiko Inamasu1, Miyako Kojo1, Yoshimasa Shiraishi1, Yosuke Morodomi1, Tomoyoshi Takenaka1, Fumihiko Hirai1, Masafumi Yamaguchi1, Takashi Seto1, Mototsugu Shimokawa4, Yukito Ichinose1.
Abstract
Anaplastic lymphoma kinase (ALK) fuses echinoderm microtubule-associated protein-like 4 (EML4) to acquire a transforming activity in lung adenocarcinomas. However, the presence of an EML4-ALK fusion gene in other lung cancer histologies is an extremely rare phenomenon. A 43-year-old female was referred to our department due to dyspnea on effort and left back pain. Computed tomography (CT) showed a large mass in the upper lobe of the left lung and a massive left pleural effusion, while a CT-guided needle biopsy confirmed a diagnosis of small-cell lung cancer (SCLC). Surprisingly, the tumor was genetically considered to harbor the EML4-ALK fusion gene (variant 2). Although the patient underwent two regimens of cytotoxic chemotherapy for SCLC, she died approximately seven months after the administration of first-line chemotherapy. Our analysis of 30 consecutive patients with SCLC for EML4-ALK revealed that two patients, including the current patient and a patient we previously reported, harbored the EML4-ALK fusion gene.Entities:
Keywords: EML4-ALK; Oncogenic driver mutation; Small-cell lung cancer
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Year: 2013 PMID: 23787064 DOI: 10.1016/j.lungcan.2013.05.022
Source DB: PubMed Journal: Lung Cancer ISSN: 0169-5002 Impact factor: 5.705