alk驱动的非小细胞肺癌:述评-第一部分

Q1 Medicine
S. Nathany, M. Sharma, U. Batra
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引用次数: 2

摘要

间变性淋巴瘤激酶(ALK)重排非小细胞肺癌(NSCLC)是一种分子上独特的癌基因依赖性非小细胞肺癌亚群,占病例的3-5%。这些主要是导致融合癌蛋白的基因组重排,从而导致持续的构成信号。最近几代ALK抑制剂的开发和批准已经改变了这种疾病的治疗和预后前景。为了准备本综述,我们检索了PubMed、Embase和Scopus等多个数据库,检索关键词为“ALK”、“ALK crizotinib”、“Oncogene NSCLC”和“Alectinib”,最终纳入了46篇文章。本文就alk重排非小细胞肺癌的分子生物学、病理及临床特点作一综述。检测方法、治疗策略和试验将在本生物标志物综述系列的下一部分进行讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ALK-driven NSCLC: A narrative review - Part I
Anaplastic lymphoma kinase (ALK)-rearranged non-small-cell lung cancer (NSCLC) is a molecularly distinct subgroup of oncogene-addicted NSCLC, accounting for 3-5% of cases. These are mainly genomic rearrangements resulting in a fusion oncoprotein, thus causing persistent constitutive signaling. Recent developments and approvals of various generations of ALK inhibitors have revamped the therapeutic and prognostic landscape of this disease entity. For the preparation of this review, we searched various databases such as PubMed, Embase, and Scopus, using the keywords “ALK,” “ALK crizotinib,” “Oncogene NSCLC,” and “Alectinib,” and we finally included 46 articles. In this review, we describe the molecular biology and pathologic and clinical characteristics of ALK-rearranged NSCLC. The detection methods, therapeutic strategies, and trials will be discussed in the next part of this biomarker review series.
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来源期刊
CiteScore
5.00
自引率
0.00%
发文量
142
审稿时长
13 weeks
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