间变性淋巴瘤激酶
医学
克里唑蒂尼
肺癌
腺癌
融合基因
肿瘤科
癌症研究
内科学
癌症
基因
遗传学
生物
恶性胸腔积液
作者
Zhengfu He,Xingyu Zhu,Qingxin Zeng,Zhaonan Yu
出处
期刊:Lung Cancer
[Elsevier]
日期:2021-06-08
卷期号:158: 164-165
被引量:1
标识
DOI:10.1016/j.lungcan.2021.06.006
摘要
With the development of next generation sequencing(NGS), more and more novel ALK fusion partners have been reported since the discovery of anaplastic lymphoma kinase fusion-positive (ALK+) NSCLC (EML4-ALK) in 2007 [1]. The pace that new fusion partners are being identified and reported has rapidly increased since 2018. According to the report, distinct 5’ fusion partners identified in ALK + NSCLC are up to 90 by the end of January 2020 [2]. However the need to identify rare actionable driver mutations are still urgent and unmet.
科研通智能强力驱动
Strongly Powered by AbleSci AI