Skip to main navigation Skip to search Skip to main content

Pharmacokinetic evaluation of axitinib

  • University of Pennsylvania
  • Fox Chase Cancer Center
  • Hospital Clinico Universitario de Valencia
  • Departments of Medical Oncology
  • University of Texas Health Science Center at San Antonio

Research output: Contribution to journal › Review article › peer-review

29 Scopus citations

Abstract

The role of angiogenic inhibitors is clearly established in the treatment of diverse malignancies. The field of antiangiogenesis is expanding rapidly, with an increasing number of agents currently approved by the FDA. Axitinib is a vascular endothelial growth factor receptor (VEGFR)-specific inhibitor currently being developed for the treatment of various malignancies. The pharmacokinetic (PK) properties of axitinib may provide a selective treatment effect while minimizing adverse reactions and enhancing safety. It is paramount that health-care providers understand the properties and nuances of each agent inclusive of PK variability in the patient population as well as current safety and tolerability data. Areas covered: This article provides a comprehensive and critical review of the PK properties of axitinib as they relate to safety and tolerability, as well as potential pharmacodynamic and efficacy parameters. Expert opinion: Axitinib is a unique VEGFR tyrosine kinase inhibitor (TKI), which acts through greater receptor specificity compared with many other VEGFR TKIs. An understanding of axitinib's PK characteristics and common adverse events may allow for a tailored dosing approach in patients with cancer, in an attempt to maximize efficacy while minimizing toxicity.

Original languageEnglish
Pages (from-to)259-270
Number of pages12
JournalExpert Opinion on Drug Metabolism and Toxicology
Volume8
Issue number2
DOIs
StatePublished - Jan 2012

Keywords

  • AG-013736
  • VEGF
  • VEGFR
  • angiogenesis
  • axitinib
  • vascular endothelial growth factor

Fingerprint

Dive into the research topics of 'Pharmacokinetic evaluation of axitinib'. Together they form a unique fingerprint.

Cite this