학술논문

Sorafenib dose escalation is not uniformly associated with blood pressure elevations in normotensive patients with advanced malignancies.
Document Type
article
Source
Clinical pharmacology and therapeutics. 96(1)
Subject
Humans
Neoplasms
Neoplasm Metastasis
Phenylurea Compounds
Niacinamide
Receptors
Vascular Endothelial Growth Factor
Prospective Studies
Blood Pressure
Dose-Response Relationship
Drug
Adult
Aged
Middle Aged
Female
Male
Young Adult
Sorafenib
Receptors
Vascular Endothelial Growth Factor
Dose-Response Relationship
Drug
Pharmacology and Pharmaceutical Sciences
Pharmacology & Pharmacy
Language
Abstract
Hypertension after treatment with vascular endothelial growth factor (VEGF) receptor inhibitors is associated with superior treatment outcomes for advanced cancer patients. To determine whether increased sorafenib doses cause incremental increases in blood pressure (BP), we measured 12-h ambulatory BP in 41 normotensive advanced solid tumor patients in a randomized dose-escalation study. After 7 days' treatment (400 mg b.i.d.), mean diastolic BP (DBP) increased in both study groups. After dose escalation, group A (400 mg t.i.d.) had marginally significant further increase in 12-h mean DBP (P = 0.053), but group B (600 mg b.i.d.) did not achieve statistically significant increases (P = 0.25). Within groups, individuals varied in BP response to sorafenib dose escalation, but these differences did not correlate with changes in steady-state plasma sorafenib concentrations. These findings in normotensive patients suggest BP is a complex pharmacodynamic biomarker of VEGF inhibition. Patients have intrinsic differences in sensitivity to sorafenib's BP-elevating effects.