The coming of ramucirumab in the landscape of anti-angiogenic drugs: potential clinical and translational perspectives

被引:13
作者
Calvetti, Lorenzo [1 ]
Pilotto, Sara [1 ]
Carbognin, Luisa [1 ]
Ferrara, Roberto [1 ]
Caccese, Mario [1 ]
Tortora, Giampaolo [1 ]
Bria, Emilio [1 ]
机构
[1] Univ Verona, Univ Integrata, Azienda Ospedaliera, Med Oncol, I-37124 Verona, Italy
关键词
angiogenesis; gastric cancer; ramucirumab; review; ENDOTHELIAL GROWTH-FACTOR; MONOCLONAL-ANTIBODY; TUMOR ANGIOGENESIS; 1ST-LINE THERAPY; DOUBLE-BLIND; PHASE-I; COLORECTAL-CARCINOMA; OPEN-LABEL; CANCER; BEVACIZUMAB;
D O I
10.1517/14712598.2015.1071350
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 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Angiogenesis plays a pivotal role in the development and progression of tumors and it represents a crucial target for therapeutic strategies. Until now, regulatory agencies approved antiangiogenic agents targeting the VEGF and multi-target agents carrying antiangiogenic and anti-proliferative effects. They often provide only a modest survival benefit and their role in clinical practice is debated. The limited efficacy may be partially explained by the complexity of the molecular background of angiogenic processes, composed of several pathways interacting with both tumor cells and the microenvironment. Areas covered: Ramucirunnab is a fully human monoclonal antibody selectively binding and inhibiting the VEGF receptor 2 (VEGFR-2), a crucial molecule involved in angiogenesis. A series of Phase I-II trials conducted in a wide spectrum of malignancies reported promising antitumor activity. In 2014, data from large Phase III clinical trials in gastrointestinal, lung and breast malignancies were released. Expert opinion: Considering the evidences of efficacy emerging from the available Phase III trials, the antiangiogenic approach emerged as a promising strategy particularly for the treatment of gastric cancer. Nevertheless, the identification and validation of potentially predictive biomarkers are necessary to improve the selection of patients and the globally awaited clinical benefit.
引用
收藏
页码:1359 / 1370
页数:12
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