Rationally combining anti-VEGF therapy with checkpoint inhibitors in hepatocellular carcinoma

被引:136
作者
Hato, Tai [1 ,2 ]
Zhu, Andrew X. [3 ]
Duda, Dan G. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Edwin L Steele Labs,Dept Radiat Oncol, Boston, MA 02114 USA
[2] Keio Univ, Sch Med, Dept Surg, Tokyo 1608582, Japan
[3] Harvard Univ, Sch Med, Hematol Oncol, Dept Med,Massachusetts Gen Hosp,Canc Ctr, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
CTLA-4; hepatocellular carcinoma; immune checkpoint; LAG-3; PD-1; PD-L1; TIM-3; VEGF; VEGFR2; ENDOTHELIAL GROWTH-FACTOR; T-CELL RESPONSES; CHRONIC HEPATITIS-C; NATURAL-KILLER-CELLS; DENDRITIC CELLS; TUMOR MICROENVIRONMENT; ADENOSINE RECEPTOR; ANTITUMOR IMMUNITY; SUPPRESSOR-CELLS; KINASE INHIBITOR;
D O I
10.2217/imt.15.126
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatocellular carcinoma (HCC) is a fatal disease with rising incidence in the world. For advanced HCC, sorafenib, a multikinase inhibitor, is the only systemic therapy with proven survival benefits. Sorafenib is a pan-VEGF receptor inhibitor, and thus many studies have focused its antivascular effects. But VEGF also acts as an immunosuppressive molecule. VEGF can inhibit maturation of dendritic cells, promote immune suppressive cell infiltration and enhance immune checkpoint molecules expression. On the other hand, potent VEGF inhibition may increase tumor hypoxia, which could hinder antitumor immunity or immunotherapy. Thus, achieving synergy when combining anti-VEGF therapy with immunotherapy may require proper polarization of the tumor microenvironment by dose titration or combination with other immunomodulating agents.
引用
收藏
页码:299 / 313
页数:15
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