Clinical consequences of resistance to ALK inhibitors in non-small cell lung cancer

被引:9
|
作者
Pinto, Joseph A. [1 ]
Raez, Luis E. [2 ]
Domingo, Gelenis [2 ]
机构
[1] Oncosalud AUNA, Unidad Invest Basica & Traslac, Lima, Peru
[2] Florida Int Univ, Mem Canc Inst, Thorac Oncol Program, Mem Hlth Care Syst, Miami, FL 33199 USA
关键词
Non-small cell lung cancer; ALK; tyrosine-kinase inhibitors; OPEN-LABEL; CRIZOTINIB RESISTANCE; METASTATIC SPREAD; CERITINIB; CHEMOTHERAPY; MULTICENTER; MECHANISMS; ALECTINIB; THERAPY; BIOLOGY;
D O I
10.1080/17476348.2020.1721285
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: ALK rearrangements are present in 2-7% of non-small cell lung cancer (NSCLC) cases, where the EML4-ALK fusion is the most frequent. Rearrangement of ALK with other fusion partners occurs only in approximate to 5% of NSCLC ALK-positive. These patients have benefited from ALK inhibitors, and currently, there are three generations of drugs as the standard of care. The first-generation ALK inhibitor crizotinib is approved in the front-line setting for the treatment of advanced NSCLC; unfortunately, these tumors may eventually develop resistance to this molecule. The Second-generation ALK inhibitors, ceritinib, alectinib, and brigatinib, are approved for patients recently diagnosed or in relapse. The third-generation inhibitor lorlatininb is approved for patients who have developed resistance to any ALK inhibitor. Areas covered: In this review, an unstructured search in Pubmed and SCOPUS was conducted. We summarized the mechanisms of resistance to ALK inhibitors and its consequences in the treatment-decision making in advanced or metastatic NSCLC after failure to a first-line ALK inhibitor. Expert opinion: Currently, there are a growing number of options of therapeutic agents against ALK+ NSCLC (approved and in development); however, adequate selection and sequencing of agents are crucial to deal with the tumor evolution.
引用
收藏
页码:385 / 390
页数:6
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