Targeted therapies for small cell lung cancer: Where do we stand?

被引:50
作者
Arcaro, Alexandre [1 ]
机构
[1] Univ Bern, Dept Clin Res, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Small cell lung cancer; Receptor tyrosine kinase; Angiogenesis; Apoptosis; Epigenetics; Immunotherapy; ENDOTHELIAL GROWTH-FACTOR; PHASE-II TRIAL; BCL-2 ANTISENSE OLIGONUCLEOTIDE; COMPREHENSIVE GENOMIC ANALYSIS; INHIBITOR PANOBINOSTAT LBH589; POTENTIAL THERAPEUTIC TARGET; PACLITAXEL PLUS BEVACIZUMAB; RECEPTOR KINASE INHIBITOR; HOOSIER-ONCOLOGY-GROUP; IN-VITRO;
D O I
10.1016/j.critrevonc.2015.03.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Small cell lung cancer (SCLC) accounts for 15% of lung cancer cases and is associated with a dismal prognosis. Standard therapeutic regimens have been improved over the past decades, but without a major impact on patient survival. The development of targeted therapies based on a better understanding of the molecular basis of the disease is urgently needed. At the genetic level, SCLC appears very heterogenous, although somatic mutations targeting classical oncogenes and tumor suppressors have been reported. SCLC also possesses somatic mutations in many other cancer genes, including transcription factors, enzymes involved in chromatin modification, receptor tyrosine kinases and their downstream signaling components. Several avenues have been explored to develop targeted therapies for SCLC. So far, however, there has been limited success with these targeted approaches in clinical trials. Further progress in the optimization of targeted therapies for SCLC will require the development of more personalized approaches for the patients. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:154 / 164
页数:11
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