Treatment and Implications of Vascular Endothelial Growth Factor Inhibitor‐Induced Blood Pressure Rise: A Clinical Cohort Study

Author:

van Dorst Daan C. H.12ORCID,Kabadayi Sumeyye3ORCID,Oomen‐de Hoop Esther1ORCID,Danser A.H. Jan2ORCID,Mathijssen Ron H. J.1ORCID,Versmissen Jorie23ORCID

Affiliation:

1. Department of Medical Oncology, Erasmus MC Cancer Institute Erasmus MC University Medical Center Rotterdam The Netherlands

2. Division of Vascular Medicine and Pharmacology, Department of Internal Medicine Erasmus MC University Medical Center Rotterdam The Netherlands

3. Department of Hospital Pharmacy Erasmus MC University Medical Center Rotterdam The Netherlands

Abstract

Background Anti‐cancer vascular endothelial growth factor inhibitors (VEGFI) frequently induce a rise in blood pressure (BP). The most effective treatment of this BP rise is currently unknown, and risk factors and its association with survival remain inconclusive. Methods and Results Baseline characteristics and BP readings were retrospectively collected from oncology patients who received oral VEGFI treatment (sorafenib, sunitinib, pazopanib, regorafenib, lenvatinib, or cabozantinib). Risk factors for a clinically relevant BP rise (increase of ≥20 mm Hg in systolic BP or ≥10 mm Hg in diastolic BP) were investigated via logistic regression (relative), efficacy of antihypertensives via unpaired t‐tests, and association of BP rise with survival via Cox regression analysis. In total, 162 (47%) of 343 included patients developed a clinically relevant BP rise ≥7 days after VEGFI treatment initiation. Both calcium channel blockers and renin‐angiotensin system inhibitors effectively reduced systolic BP (−24.1 and −18.2 mm Hg, respectively) and diastolic BP (−12.0 and −11.0 mm Hg, respectively). Pazopanib therapy (odds ratio, 2.71 [95% CI, 1.35–5.42; P =0.005], compared with sorafenib) and estimated glomerular filtration rate <60 mL/min per 1.73 m 2 (OR, 1.75 [95% CI, 0.99–3.18, P =0.054]) were risk factors for a BP rise, whereas a baseline BP ≥140/90 mm Hg associated with a lower risk (OR, 0.39 [95% CI, 0.25–0.62, P <0.001]). Only for renal cell carcinoma, BP rise was associated with a substantially improved median overall survival compared with no BP rise: 45.4 versus 20.3 months, respectively, P =0.003. Conclusions The type of VEGFI, baseline BP, and baseline estimated glomerular filtration rate determine the VEGFI‐induced BP rise. Both calcium channel blockers and renin‐angiotensin system inhibitors are effective antihypertensive treatments. Particularly in patients with renal cell carcinoma, a BP rise is associated with improved overall survival.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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