4.2 Review

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

期刊

IMMUNOTHERAPY
卷 8, 期 3, 页码 299-313

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/imt.15.126

关键词

CTLA-4; hepatocellular carcinoma; immune checkpoint; LAG-3; PD-1; PD-L1; TIM-3; VEGF; VEGFR2

资金

  1. National Institutes of Health [P01-CA080124, R01-CA159258, R21-CA139168]
  2. National Cancer Institute/Proton Beam Federal Share Program award
  3. American Cancer Society [120733-RSG-11-073-01-TBG]

向作者/读者索取更多资源

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.

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