Intercalation of Erlotinib and Pemetrexed in the Treatment of Non-Small Cell Lung Cancer

被引:7
|
作者
Li, Tianhong [1 ]
Lara, Primo N., Jr. [1 ]
Mack, Philip C. [1 ]
Perez-Soler, Roman [1 ]
Gandara, David R. [1 ]
机构
[1] Univ Calif Davis, Ctr Canc, Div Hematol & Oncol, Sacramento, CA 95817 USA
关键词
Pemetrexed; multi-targeted antifolate; erlotinib; small molecule tyrosine kinase inhibitor (TKI); epidermal growth factor receptor (EGFR); non-small cell lung cancer (NSCLC); GROWTH-FACTOR-RECEPTOR; PHASE-III TRIAL; TYROSINE KINASE INHIBITORS; MULTITARGETED ANTIFOLATE LY231514; CHEMOTHERAPY-NAIVE PATIENTS; CISPLATIN PLUS GEMCITABINE; FRONT-LINE THERAPY; COMPARING CISPLATIN; ACQUIRED-RESISTANCE; ANTITUMOR-ACTIVITY;
D O I
10.2174/138945010790030983
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Both the multi-targeted antifolate pemetrexed and the epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) erlotinib have established roles in the treatment of advanced non-small cell lung cancer (NSCLC). Given different mechanisms of action and minimal overlapping toxicities, combinations of these agents have been considered. However, four previous phase III trials investigating concurrent chemotherapy with or without EGFR TKIs showed no clinical benefit. Based on preclinical data, we developed a model of pharmacodynamic separation to avoid potential negative interactions between chemotherapy and EGFR TKIs in NSCLC tumors containing wild-type EGFR gene. This review summarizes the background, scientific rationale and early clinical data in support of intercalation of intermittent erlotinib dosing with pemetrexed as a means of achieving pharmacodynamic separation. Ongoing research efforts investigating this concept are reviewed.
引用
收藏
页码:85 / 94
页数:10
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