Dacomitinib, a new therapy for the treatment of non-small cell lung cancer

被引:32
|
作者
Brzezniak, Christina [1 ]
Carter, Corey A. [1 ]
Giaccone, Giuseppe [2 ]
机构
[1] Walter Reed Natl Mil Med Ctr, Bethesda, MD 20889 USA
[2] NCI, Med Oncol Branch, Bethesda, MD 20892 USA
关键词
dacomitinib; EGFR tyrosine kinase; non-small cell lung cancer; pan-HER; PF-00299804; T790M; EPIDERMAL-GROWTH-FACTOR; TYROSINE KINASE INHIBITORS; FACTOR RECEPTOR MUTATIONS; RANDOMIZED PHASE-II; ACQUIRED-RESISTANCE; DRUG-RESISTANCE; GEFITINIB; EGFR; ERLOTINIB; PF-00299804;
D O I
10.1517/14656566.2013.758714
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Advanced or metastatic non-small cell lung cancer (NSCLC) is characterized by a poor prognosis and few second-or third-line treatments. First-generation reversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibition (TKI) has paved the way for targeted treatment in lung cancer. These drugs result in excellent responses in patients with activating EGFR mutations. Unfortunately, resistance often develops. Second-generation irreversible inhibitors hope to prevent mutational progression to a resistant clone or delay the use of alternative non-targeted therapies. Areas covered: This article focuses on the current published ongoing research using the second-generation irreversible TKI, dacomitinib. The use of dacomitinib, a pan inhibitor of the HER family of tyrosine kinases, will be reviewed along with its efficacy in the advanced or metastatic NSCLC population. Expert opinion: Data available suggest dacomitinib is effective in NSCLC patients both in initial treatment and after failure of first-generation inhibitors. Furthermore, preclinical data suggest dacomitinib can achieve responses in tumors harboring the T790M, gatekeeper mutation, present in up to 50% of tumors that have acquired resistant to first-generation inhibitors. Its usefulness in potentially delaying development of resistant clones as well as in combination with other targeting strategies is under investigation.
引用
收藏
页码:247 / 253
页数:7
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