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用于非小细胞肺癌的I期和II期临床试验中的间变性淋巴瘤激酶抑制剂

Anaplastic lymphoma kinase inhibitors in phase I and phase II clinical trials for non-small cell lung cancer.

作者信息

Karachaliou Niki, Santarpia Mariacarmela, Gonzalez Cao Maria, Teixido Cristina, Sosa Aaron E, Berenguer Jordi, Rodriguez Capote Alejandra, Altavilla Giuseppe, Rosell Rafael

机构信息

a Institute of Oncology Rosell (IOR), University Hospital Sagrat Cor , Barcelona , Spain.

b Medical Oncology Unit, Department of Human Pathology 'G. Barresi,' University of Messina , Messina , Italy.

出版信息

Expert Opin Investig Drugs. 2017 Jun;26(6):713-722. doi: 10.1080/13543784.2017.1324572. Epub 2017 May 18.

DOI:10.1080/13543784.2017.1324572
PMID:28463570
Abstract

Crizotinib is a first-in-class ALK tyrosine kinase inhibitor (TKI), which has proven its superiority over standard platinum-based chemotherapy for the first-line therapy of ALK-rearranged non-small cell lung cancer (NSCLC) patients. The development of acquired resistance to crizotinib represents an ongoing challenge with the central nervous system being one of the most common sites of relapse. Ceritinib and alectinib are approved second-generation ALK TKIs. Several novel ALK inhibitors, more potent and with different selectivity compared to crizotinib, are currently in development. Areas covered: This review will focus on new ALK inhibitors, currently in phase 1 or 2 clinical studies. We will also comment on the mechanisms of resistance to ALK inhibition and the strategies to delay or overcome resistance. Expert opinion: The therapeutic management of ALK-rearranged NSCLC has been greatly improved. Next-generation ALK inhibitors have shown differential potency against ALK rearrangements and ALK resistance mutations. The molecular profile of the tumor at the time of disease progression to crizotinib is crucial for the sequencing of novel ALK TKIs. Ongoing clinical studies will address key issues, including the optimal therapeutic algorithm and whether combinational approaches are more effective than single ALK inhibition for the outcome of ALK-rearranged NSCLC patients.

摘要

克唑替尼是首个上市的间变性淋巴瘤激酶(ALK)酪氨酸激酶抑制剂(TKI),已证实其在一线治疗ALK重排的非小细胞肺癌(NSCLC)患者方面优于标准铂类化疗。对克唑替尼产生获得性耐药是一个持续存在的挑战,中枢神经系统是最常见的复发部位之一。色瑞替尼和阿来替尼是已获批的第二代ALK TKI。目前正在研发几种新型ALK抑制剂,它们比克唑替尼更有效且具有不同的选择性。涵盖领域:本综述将聚焦于目前处于1期或2期临床研究的新型ALK抑制剂。我们还将对ALK抑制的耐药机制以及延迟或克服耐药的策略进行评论。专家观点:ALK重排NSCLC的治疗管理已得到极大改善。新一代ALK抑制剂对ALK重排和ALK耐药突变显示出不同的效力。疾病进展至克唑替尼时肿瘤的分子特征对于新型ALK TKI的序贯治疗至关重要。正在进行的临床研究将解决关键问题,包括最佳治疗方案以及联合治疗方法对ALK重排NSCLC患者的疗效是否比单一ALK抑制更有效。

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