Smolle Elisabeth, Taucher Valentin, Lindenmann Joerg, Jost Philipp J, Pichler Martin
Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, 8036 Graz, Austria.
Division of Cardiology, Department of Internal Medicine, Hospital Barmherzige Schwestern Ried, 4910 Ried, Austria.
Cancers (Basel). 2021 Feb 9;13(4):699. doi: 10.3390/cancers13040699.
Non-small cell lung cancer (NSCLC) accounts for the majority of lung cancer subtypes. Two to seven percent of NSCLC patients harbor gene rearrangements of the anaplastic lymphoma kinase (ALK) gene or, alternatively, harbor chromosomal fusions of ALK with echinoderm microtubule-associated protein-like 4 (EML4). The availability of tyrosine kinase inhibitors targeting ALK (ALK-TKIs) has significantly improved the progression-free and overall survival of NSCLC patients carrying the respective genetic aberrations. Yet, increasing evidence shows that primary or secondary resistance to ALK-inhibitors during the course of treatment represents a relevant clinical problem. This necessitates a switch to second- or third-generation ALK-TKIs and a close observation of NSCLC patients on ALK-TKIs during the course of treatment by repetitive molecular testing. With this review of the literature, we aim at providing an overview of current knowledge about resistance mechanisms to ALK-TKIs in NSCLC.
非小细胞肺癌(NSCLC)占肺癌亚型的大多数。2%至7%的NSCLC患者存在间变性淋巴瘤激酶(ALK)基因重排,或者存在ALK与棘皮动物微管相关蛋白样4(EML4)的染色体融合。靶向ALK的酪氨酸激酶抑制剂(ALK-TKIs)的出现显著改善了携带相应基因异常的NSCLC患者的无进展生存期和总生存期。然而,越来越多的证据表明,治疗过程中对ALK抑制剂的原发性或继发性耐药是一个相关的临床问题。这就需要改用第二代或第三代ALK-TKIs,并在治疗过程中通过重复分子检测对接受ALK-TKIs治疗的NSCLC患者进行密切观察。通过对文献的综述,我们旨在概述目前关于NSCLC中ALK-TKIs耐药机制的知识。