阿列克替尼
间变性淋巴瘤激酶
克里唑蒂尼
医学
肺癌
碱性抑制剂
融合基因
癌症研究
基因重排
肿瘤科
生物
基因
生物化学
恶性胸腔积液
作者
Liang Qi,Huanhuan Xu,Yiqian Liu,Weimin Zhang,Chongqi Sun,Meng Hu,Yi-Zhi Zhu,Shanyue Tan,Xian Xu,Sumeng Wang,Lingxiang Liu
出处
期刊:Lung Cancer
[Elsevier BV]
日期:2021-12-01
卷期号:162: 86-89
被引量:5
标识
DOI:10.1016/j.lungcan.2021.10.015
摘要
The echinoderm microtubule-associated protein-like 4 gene (EML4) and anaplastic lymphoma kinase gene (ALK) fusion is the most common ALK rearrangements in non-small cell lung cancer (NSCLC). Herein, we firstly report that coexistence of a novel Neurobeachin (NBEA)-ALK, EML4-ALK double-fusion is sensitive to alectinib.Hematoxylin-eosin staining (HE), fluorescent in situ hybridization (FISH), and next-generation sequencing (NGS) was performed on the biopsy sample.The patient responded to alectinib as a second-line treatment and achieved stable disease for 11 months, without significant symptoms of toxicity. Significantly, the liquid biopsy also validated clinical benefit, with the disappearance of NBEA-ALK and EML4-ALK fusion variants. We also provided a comprehensive review of all 50 ALK fusion genes in NSCLC.This is the first report on one patient with a novel NBEA-ALK, EML4-ALK double-ALK fusion beneficial from alectinib. Alectinib may be a viable therapeutic option for NSCLC patients with double-ALK fusion, and liquid biopsy could dynamically monitor clinical curative effect.
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