Novel agents in development for advanced non-small cell lung cancer

被引:32
作者
Stinchcombe, Thomas E. [1 ]
机构
[1] Univ N Carolina, Chapel Hill, NC 27599 USA
关键词
anaplastic lymphoma kinase; dacomitinib; epidermal growth factor receptor; ganetespib; nintedanib; onartuzumab; targeted therapy; tivantinib; GROWTH-FACTOR RECEPTOR; RANDOMIZED PHASE-II; TYROSINE KINASE INHIBITORS; ACQUIRED-RESISTANCE; OPEN-LABEL; INTEROBSERVER AGREEMENT; 1ST-LINE TREATMENT; CYTOTOXIC ACTIVITY; TUMOR SPECIMENS; GENE-MUTATIONS;
D O I
10.1177/1758834014532510
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The identification of EGFR mutations and ALK rearrangements in nonsmall cell lung cancer (NSCLC) has led to the rapid development of targeted therapies and significant changes in the treatment paradigm. Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) and crizotinib are now standard therapies for patients with the appropriate molecular alteration. Current investigations are determining the mechanisms of resistance to targeted therapies and developing novel agents to combat resistance. For patients with KRAS mutant NSCLC, a phase III trial of the MEK inhibitor, selumetinib, has been initiated. For patients without a defined mutation or a mutation without a known targeted therapy, immunotherapy, ganetespib, nintedanib and MET inhibitors in combination with EGFR TKIs are in development. Preliminary results of phase III trials raise doubts about the future development of dacomitinib as a second-line agent.
引用
收藏
页码:240 / 253
页数:14
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