Current Status of Targeted Therapy for Anaplastic Lymphoma Kinase-Rearranged Non-Small Cell Lung Cancer

被引:76
|
作者
Solomon, B. [1 ,2 ]
Wilner, K. D. [3 ]
Shaw, A. T. [4 ]
机构
[1] Peter MacCallum Canc Ctr, Dept Med Oncol, East Melbourne, Vic, Australia
[2] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic, Australia
[3] Pfizer, La Jolla, CA USA
[4] Massachusetts Gen Hosp, Ctr Canc, Dept Med, Boston, MA 02114 USA
关键词
ALK GENE REARRANGEMENT; RECEPTOR TYROSINE KINASE; EML4-ALK FUSION GENE; CRIZOTINIB RESISTANCE; ACTIVATING MUTATIONS; ONCOGENIC MUTATIONS; CLINICAL-FEATURES; NEVER-SMOKERS; PHASE-II; INHIBITOR;
D O I
10.1038/clpt.2013.200
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The identification of chromosomal rearrangements involving the anaplastic lymphoma kinase (ALK) gene in similar to 3-5% of non-small cell lung cancer (NSCLC) tissues and the demonstration that the first-in-class ALK tyrosine kinase inhibitor, crizotinib, can effectively target these tumors represent a significant advance in the evolution of personalized medicine for NSCLC. Single-arm studies demonstrating rapid and durable responses in the majority of ALK-positive NSCLC patients treated with crizotinib have been followed by a randomized phase Ill clinical trial in which superiority of crizotinib over chemotherapy was seen in previously treated ALK-positive NSCLC patients. However, despite the initial responses, most patients develop acquired resistance to crizotinib. Several novel therapeutic approaches targeting ALK-positive NSCLC are currently under evaluation in clinical trials, including second-generation ALK inhibitors, such as LDK378, CH5424802 (RO5424802802), and AP26113, and heat shock protein 90 inhibitors.
引用
收藏
页码:15 / 23
页数:9
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