VEGF inhibitors in brain tumors

Priscilla K Brastianos1, Tracy T Batchelor

  • 1Department of Medical Oncology, Dana-Farber/Brigham and Women's Cancer Center, Massachusetts General Hospital, Boston, 02114, USA.

Insights

Glioblastoma treatments targeting tumor vascularity show promise but ultimately fail. Further research is crucial to overcome resistance and find new therapeutic targets for angiogenesis in brain tumors.

Area of Science:

  • Oncology
  • Cancer Biology
  • Vascular Biology

Background:

  • Glioblastomas are characterized by significant vascularity.
  • Angiogenesis, the formation of new blood vessels, is a key process in glioblastoma growth.
  • Targeting angiogenesis has emerged as a potential therapeutic strategy for glioblastomas.

Purpose of the Study:

  • To review current therapeutic strategies targeting angiogenesis in glioblastomas.
  • To highlight the limitations and inevitable treatment failure observed.
  • To emphasize the need for further research into resistance mechanisms and novel therapeutic targets.

Main Methods:

  • Review of preclinical and clinical investigations.
  • Analysis of therapeutic agents targeting vascular endothelial growth factor (VEGF) and its pathways.
  • Examination of immunomodulatory agents and soluble decoy VEGF receptors.

Main Results:

  • Various anti-angiogenic agents, including anti-VEGF antibodies and tyrosine kinase inhibitors, are under investigation.
  • Despite initial promise, current anti-angiogenic therapies for glioblastoma inevitably lead to treatment failure.
  • Tumor resistance to these therapies is a significant clinical challenge.

Conclusions:

  • While targeting angiogenesis is a rational approach for glioblastomas, current treatments are not curative.
  • Understanding the mechanisms underlying tumor resistance is critical for developing more effective therapies.
  • Identification of alternative therapeutic targets that mediate angiogenesis is essential for future treatment strategies.

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