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

Tai Hato, Andrew X. Zhu, Dan G. Duda

Research output: Contribution to journalReview articlepeer-review

Abstract

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.

Original languageEnglish (US)
Pages (from-to)299-313
Number of pages15
JournalImmunotherapy
Volume8
Issue number3
DOIs
StatePublished - Mar 2016

Keywords

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

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology
  • Oncology

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