Enhancing the efficacy of VEGF inhibitors by co-inhibition of HIF in the treatment of glioblastoma. Review uri icon

Overview

abstract

  • Glioblastoma is the most aggressive and most common grade 4 tumor of the central nervous system (CNS). Despite standard treatments such as surgical resection and chemoradiotherapy, overall survival (OS) usually does not exceed 14-16 months in clinical trials, and no improvement in OS has been demonstrated even with the use of vascular endothelial growth factor A (VEGFA) inhibitors such as bevacizumab. In response to radiotherapy, hypoxia-inducible factor (HIF) stabilization leads to activation of alternative pro-angiogenic pathways, increasing VEGF expression and tumor angiogenesis. Several clinical trials evaluating HIF-2α inhibitors as monotherapy in the absence of concurrent VEGF inhibition, have similarly failed to demonstrate a significant improvement in OS outcomes. This review provides a perspective on the combined use of VEGF and HIF inhibitors, and provides an insight into future studies.

publication date

  • January 23, 2026

Research

keywords

  • Angiogenesis Inhibitors
  • Basic Helix-Loop-Helix Proteins
  • Brain Neoplasms
  • Glioblastoma
  • Vascular Endothelial Growth Factor A

Identity

PubMed Central ID

  • PMC12830476

Scopus Document Identifier

  • 105028350111

Digital Object Identifier (DOI)

  • 10.1007/s10495-026-02275-5

PubMed ID

  • 41575610

Additional Document Info

volume

  • 31

issue

  • 2