Affiliation:
1. BuChang (Beijing) Pharmaceutical Co. Ltd, Hongda Industrial Park, Hongda North Road, Beijing 100176, China
Abstract
The vascular endothelial growth factor (VEGF)/VEGF receptor 2 (VEGFR2) signaling
pathway is one of the most important pathways responsible for tumor angiogenesis. Currently, two
monoclonal antibodies, anti-VEGF-A antibody Bevacizumab and anti-VEGFR2 antibody Ramucizumab,
have been approved for the treatment of solid tumors. At the same time, VEGF/VEGFR2
signaling is involved in the regulation of immune responses. It is reported that the inhibition of this
pathway has the capability to promote vascular normalization, increase the intra-tumor infiltration of
lymphocytes, and decrease the number and function of inhibitory immune cell phenotypes, including
Myeloid-derived suppressor cells (MDSCs), regulatory T cells (Tregs) and M2 macrophages. On
this basis, a number of clinical studies have been performed to investigate the therapeutic potential
of VEGF/VEGFR2-targeting antibodies plus programmed cell death protein 1 (PD-1)/ programmed
cell death ligand 1 (PD-L1) inhibitors in various solid tumor types. In this context, VEGF/VEGFR2-
targeting antibodies, Bevacizumab and Ramucizumab are briefly introduced, with a description of
the differences between them, and the clinical studies involved in the combination of Bevacizumab/
Ramucizumab and PD-1/PD-L1 inhibitors are summarized. We hope this review article will
provide some valuable clues for further clinical studies and usages.
Publisher
Bentham Science Publishers Ltd.
Subject
Cancer Research,Drug Discovery,Pharmacology,Oncology
Cited by
53 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献