Targeted inhibition of VEGF receptor 2: an update on ramucirumab

被引:154
作者
Clarke, Jeffrey Melson [1 ]
Hurwitz, Herbert I. [1 ]
机构
[1] Duke Univ, Med Ctr, Duke Canc Inst, Durham, NC 27710 USA
关键词
adenocarcinoma; angiogenesis; cancer; gastric cancer; monoclonal antibody; ramucirumab; vascular endothelial growth factor; VEGFR2; ENDOTHELIAL GROWTH-FACTOR; METASTATIC COLORECTAL-CANCER; RANDOMIZED PHASE-III; GASTRIC-CANCER; TUMOR ANGIOGENESIS; 1ST-LINE THERAPY; DENDRITIC CELLS; SUPPORTIVE CARE; CHEMOTHERAPY; BEVACIZUMAB;
D O I
10.1517/14712598.2013.810717
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Introduction: Ramucirumab (IMC-1121B) is a fully humanized IgG1 monoclonal antibody, targeting the extracellular domain of VEGF receptor 2 (VEGFR2). Numerous Phase I-II trials in various malignancies have shown promising clinical antitumor efficacy and tolerability. Most recently, the large Phase III REGARD trial evaluated ramucirumab in patients with refractory metastatic gastric cancer. Patients receiving ramucirumab experienced a median overall survival of 5.2 months compared to 3.8 months on placebo. Areas covered: The purpose of this article is to review the preclinical motivation for VEGFR2-targeted therapies and survey recent data from clinical trials involving ramucirumab, as well as highlight ongoing studies. Expert opinion: Rational multi-target approaches to angiogenesis are needed to overcome resistance mechanisms. Predictive angiogenic biomarkers are also needed to optimize patient selection for novel anti-angiogenic agents.
引用
收藏
页码:1187 / 1196
页数:10
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