Hypertension induced by vascular endothelial growth factor signaling pathway inhibition: mechanisms and potential use

Emily S Robinson1, Eliyahu V Khankin, S Ananth Karumanchi

  • 1Brigham and Women's Hospital, Boston, Massachusetts, USA.

Seminars in Nephrology
|December 15, 2010
PubMed

Insights

Vascular endothelial growth factor (VEGF) targeted therapies for cancer can cause hypertension as an on-target side effect. This review explores mechanisms, clinical implications, and the potential of blood pressure increase as a biomarker for effective treatment.

Area of Science:

  • Oncology
  • Pharmacology
  • Cardiovascular Medicine

Background:

  • Vascular endothelial growth factor (VEGF) signaling pathway inhibitors are a growing class of targeted cancer therapies.
  • These therapies offer improved specificity and reduced side effects compared to traditional chemotherapy.
  • A significant side effect is hypertension, occurring in 30-80% of patients.

Purpose of the Study:

  • To review the mechanisms underlying VEGF-targeted therapy-induced hypertension.
  • To discuss the parallels between this hypertension and preeclampsia.
  • To explore therapeutic implications and the potential of hypertension as a biomarker.

Main Methods:

  • Literature review of current understanding of VEGF-targeted therapy-induced hypertension.
  • Comparative analysis of VEGF-targeted therapy-induced hypertension and preeclampsia.
  • Discussion of clinical management strategies and biomarker potential.

Main Results:

  • Hypertension is an on-target toxicity, reflecting effective VEGF pathway inhibition.
  • Similarities exist between VEGF-targeted therapy-induced hypertension and preeclampsia mechanisms.
  • Elevated blood pressure may serve as a biomarker for drug efficacy.

Conclusions:

  • Understanding the mechanisms of VEGF-targeted therapy-induced hypertension is crucial for clinical management.
  • Further research into the similarities with preeclampsia may yield therapeutic insights.
  • Monitoring blood pressure can guide dosing and confirm effective VEGF pathway inhibition.

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