ICUD-EAU International Consultation on Kidney Cancer 2010: treatment of metastatic disease. Review uri icon

Overview

abstract

  • CONTEXT: Until the development of novel targeted agents directed against angiogenesis and tumour growth, few treatment options have been available for the treatment of metastatic renal-cell carcinoma (mRCC). OBJECTIVE: This review discusses current targeted therapies for mRCC and provides consensus statements regarding treatment algorithms. EVIDENCE ACQUISITION: Medical literature was retrieved from PubMed up to April 2011. Additional relevant articles and abstract reviews were included from the bibliographies of the retrieved literature. EVIDENCE SYNTHESIS: Targeted treatment for mRCC can be categorized for the following patient groups: previously untreated patients, those refractory to immunotherapy, and those refractory to vascular endothelial growth factor (VEGF)-targeted therapy. Sunitinib and bevacizumab combined with interferon alpha are generally considered first-line treatment options in patients with favourable or intermediate prognoses. Temsirolimus is considered a first-line treatment option for poor-risk patients. Either sorafenib or sunitinib may be valid second-line treatments for patients who have failed prior cytokine-based therapies. For patients refractory to treatment with VEGF-targeted therapy, everolimus is now recommended. Pazopanib is a new treatment option in the first- and second-line setting (after cytokine failure). Sequential and combination approaches, and the roles of nephrectomy and tumour metastasectomy will also be discussed. CONCLUSIONS: Increasing clinical evidence is clarifying appropriate first- and second-line treatments with targeted agents for patients with mRCC. Based on phase 2 and 3 trials, a sequential approach is most promising, while combination therapy is still investigational. The role of nephrectomy in mRCC is being evaluated in ongoing phase 3 clinical trials.

publication date

  • June 24, 2011

Research

keywords

  • Antineoplastic Agents
  • Brain Neoplasms
  • Carcinoma, Renal Cell
  • Kidney Neoplasms
  • Lung Neoplasms
  • Pancreatic Neoplasms

Identity

Scopus Document Identifier

  • 80052263465

Digital Object Identifier (DOI)

  • 10.1016/j.eururo.2011.06.017

PubMed ID

  • 21704448

Additional Document Info

volume

  • 60

issue

  • 4