The role of alectinib in the treatment of advanced ALK-rearranged non-small-cell lung cancer

被引:6
|
作者
Srinivasamaharaj, Srividya [1 ]
Salame, Bilal Khameze [1 ]
Rios-Perez, Jorge [1 ]
Kloecker, Goetz [1 ]
Perez, Cesar A. [1 ]
机构
[1] Univ Louisville, James Graham Brown Canc Ctr, Div Med Oncol & Hematol, Louisville, KY 40292 USA
关键词
Non-small cell lung cancer; ALK gene rearrangement; alectinib; ceritinib; TYROSINE KINASE INHIBITORS; ANTITUMOR-ACTIVITY; EML4-ALK FUSION; CRIZOTINIB; RESISTANCE; CHEMOTHERAPY; MUTATIONS; EGFR; ADENOCARCINOMA; IDENTIFICATION;
D O I
10.1080/14737140.2016.1249857
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The identification of anaplastic lymphoma kinase (ALK) gene rearrangements in subsets of non-small cell lung cancer patients has provided with unparalleled opportunities to hinder the progression of this disease through targeting the activity of these specific molecules. Unfortunately most patients develop disease progression in less than a year of treatment with crizotinib, the first-generation ALK-inhibitor. Areas covered: We review the resistance mechanisms to ALK inhibitors as well as an overview of the clinical activity of the alectinib, a second generation ALK inhibitor. Expert commentary: Second generation ALK inhibitors as alectinib and ceritinib can overcome crizotinib-resistant mutations and improve central nervous system control. Novel third-generation inhibitors and combination of agents give hope of achieving an even longer disease control in the next decade.
引用
收藏
页码:1227 / 1233
页数:7
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