Angiogenesis and immune checkpoint dual blockade: Opportunities and challenges for hepatocellular carcinoma therapy

被引:11
作者
Li, Si-Qi [1 ,2 ]
Yang, Yang [1 ,2 ]
Ye, Lin-Sen [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Dept Hepat Surg, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 3, Liver Transplantat Ctr, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Anti-angiogenesis; Immunotherapy; Combination therapy; Vascular endothelial growth factor; Immune checkpoint blockade; Hepatocellular carcinoma; ENDOTHELIAL GROWTH-FACTOR; ATEZOLIZUMAB PLUS BEVACIZUMAB; DOUBLE-BLIND; CANCER-IMMUNOTHERAPY; TUMOR ANGIOGENESIS; VEGF; TRIAL; SORAFENIB; HYPOXIA; NORMALIZATION;
D O I
10.3748/wjg.v28.i42.6034
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The disease burden related to hepatocellular carcinoma (HCC) is increasing. Most HCC patients are diagnosed at the advanced stage and multikinase inhibitors have been the only treatment choice for them. Recently, the approval of immune checkpoint inhibitors (ICIs) has provided a new therapeutic strategy for HCC. It is noteworthy that the positive outcomes of the phase III clinical trial IMBrave150 [atezolizumab (anti-programmed cell death ligand 1 antibody) combined with bevacizumab (anti-vascular endothelial growth factor monoclonal antibody)], showed that overall survival and progression-free survival were significantly better with sorafenib. This combination therapy has become the new standard therapy for advanced HCC and has also attracted more attention in the treatment of HCC with anti-angiogenesis-immune combination therapy. Currently, the synergistic antitumor efficacy of this combination has been shown in many preclinical and clinical studies. In this review, we discuss the mechanism and clinical application of anti-angiogenics and immunotherapy in HCC, outline the relevant mechanism and rationality of the combined application of anti-angiogenics and ICIs, and point out the existing challenges of the combination therapy.
引用
收藏
页码:6034 / 6044
页数:12
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