The prospects of pazopanib in advanced renal cell carcinoma

Shilpa Gupta, Philippe E. Spiess

Research output: Contribution to journalArticlepeer-review

31 Scopus citations

Abstract

The landscape of treatment for advanced/metastatic renal cell carcinoma (mRCC) has advanced significantly in the last decade and continues to evolve with the approval of new drugs targeting the vascular endothelial growth factor (VEGF) and its receptors and mammalian target of rapamycin (mTOR). Currently available oral VEGF tyrosine kinase inhibitors (TKIs) approved for treatment of mRCC include sorafenib, sunitinib, pazopanib, and axitinib. This review focuses on pazopanib, a multikinase VEGF TKI indicated for patients with treatment-naïve and cytokine-refractory mRCC. This article describes the preclinical and clinical evolution of pazopanib, with an emphasis on its development and role in mRCC. Pivotal trials are discussed that demonstrate the efficacy and safety of pazopanib and its important role in the treatment of patients with mRCC in comparison to other available treatment options. The clinical path of pazopanib continues to develop further, with several ongoing studies exploring its role in neoadjuvant and adjuvant RCC. Furthermore, its potential role in sequential and combination studies with other VEGFR and non-VEGFR targeted agents is discussed. Overall, pazopanib is a unique VEGF TKI, with a different and more favorable safety profile compared with other members of the VEGF TKI family and represents an attractive alternative for patients with mRCC.

Original languageEnglish (US)
Pages (from-to)223-232
Number of pages10
JournalTherapeutic Advances in Urology
Volume5
Issue number5
DOIs
StatePublished - Oct 2013

Keywords

  • kidney cancer
  • pazopanib
  • renal cell carcinoma
  • targeted therapy
  • tyrosine kinase inhibitors
  • vascular endothelial growth factor

Fingerprint

Dive into the research topics of 'The prospects of pazopanib in advanced renal cell carcinoma'. Together they form a unique fingerprint.

Cite this