The brigatinib experience: a new generation of therapy for ALK-positive non-small-cell lung cancer

被引:3
作者
Amanam, Idoroenyi [1 ]
Gupta, Rohan [1 ]
Mambetsariev, Isa [1 ]
Salgia, Ravi [1 ]
机构
[1] City Hope Comprehens Canc Ctr, Dept Med Oncol & Res Therapeut, 1500 E Duarte Rd, Duarte, CA 91010 USA
关键词
alectinib; ALK; ALTA; brigatinib; central nervous system metastases; ceritinib; crizotinib; EML4-ALK rearrangement; lung cancer; NSCLC; EML4-ALK FUSION GENE; RECEPTOR TYROSINE KINASE; ANAPLASTIC LYMPHOMA; CRIZOTINIB RESISTANCE; CSF CONCENTRATION; OPEN-LABEL; INHIBITOR; CHEMOTHERAPY; MUTATIONS; IDENTIFICATION;
D O I
10.2217/fon-2017-0545
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer remains the leading cause of cancer deaths in the world with 1.69 million deaths in 2015. A total of 85% of lung cancer cases are non-small-cell lung cancers (NSCLCs). Driver mutations associated with anaplastic lymphoma kinase (ALK) have been identified in a variety of malignancies, including NSCLC. An ALK inhibitor (crizotinib, ceritinib and alectinib) is the preferred therapeutic approach to those advanced ALK fusion variant-positive NSCLC patients. Brigatinib, a next-generation ALK inhibitor, shows promising activity in ALK-rearranged NSCLC that have previously received crizotinib with response rates in ALTA ranging from 42-50%, intracranial response 42-67% and median progression-free survival 9.2-12.9 months. Randomized Phase III trial, ALTA-1 L is investigating brigatinib in ALK inhibitor-naive patients.
引用
收藏
页码:1897 / 1908
页数:12
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