Angiogenic inhibitors in gastric cancers and gastroesophageal junction carcinomas: A critical insight

被引:37
作者
Aprile, Giuseppe [1 ]
Ongaro, Elena [1 ]
Del Re, Marzia [2 ]
Lutrino, Stefania Eufemia [1 ]
Bonotto, Marta [1 ]
Ferrari, Laura [1 ]
Rihawi, Karim [1 ]
Cardellino, Giovanni Gerardo [1 ]
Pella, Nicoletta [1 ]
Danesi, Romano [2 ]
Fasola, Gianpiero [1 ]
机构
[1] Univ & Gen Hosp, Dept Oncol, I-33100 Udine, Italy
[2] Univ Pisa, Dept Clin & Expt Med, Clin Pharmacol Unit, I-56100 Pisa, Italy
关键词
Angiogenesis; Advanced gastric cancer; Bevacizumab; Ramucirumab; ENDOTHELIAL GROWTH-FACTOR; RANDOMIZED PHASE-III; ACTIVITY IN-VITRO; OPEN-LABEL; 1ST-LINE THERAPY; DOUBLE-BLIND; TYROSINE KINASE; VEGF-A; PERIOPERATIVE CHEMOTHERAPY; TARGETED THERAPIES;
D O I
10.1016/j.critrevonc.2015.02.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Advanced gastric cancer ranks second as the global leading cause of cancer-related death and improvements in systemic chemotherapy have reached a plateau. Advanced molecular sequencing techniques help identifying patients more likely to respond to targeted agents; nevertheless we are still far from major breakthroughs. Although antiangiogenic drugs have produced notable advances, redundant pathways or mechanisms of resistance may limit their efficacy. Novel compounds have been recently developed to specifically target VEGF receptors, PIGF, FGF, MET, and angiopoietin. Ramucirumab, a monoclonal antibody specifically directed against the VEGFR-2, has emerged as a novel therapeutic opportunity. REGARD and RAINBOW were the first phase HI studies to report the value of this strategy in gastric cancer patients, and other ongoing trials are testing novel antiangiogenic compounds. The aim of our review is to present the state-of-the-art of novel antiangiogenic compounds in advanced gastric cancer, underlying the biology, their mechanism of action, and their clinical results. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:165 / 178
页数:14
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