Novel treatments for metastatic renal cell carcinoma

Crit Rev Oncol Hematol. 2005 Sep;55(3):177-91. doi: 10.1016/j.critrevonc.2005.04.002.

Abstract

The mainstay of any curative treatment in renal cell carcinoma (RCC) is surgery. In case of metastatic disease at presentation a radical nephrectomy is recommended to good performance status patients prior to start of interferon-alfa treatment. Interferon-alpha (IFN-alpha) offers in a small but significant percentage of patients advantage in overall survival; interleukin-2 (IL-2) based therapy gives similar survival rates. To date hormonal and chemotherapy do not have a proven impact on survival. The recent new insights in the molecular biology of clear RCC has revealed a key-role for vascular endothelial growth factor (VEGF) in the stimulation of angiogenesis in this highly vascularized tumour. This opens interesting new treatment strategies including: blockage of VEGF with the monoclonal antibody bevacizumab and inhibition of VEGF receptor tyrosine kinases (with small oral molecules such as SU11248 or PTK787). Likewise, inhibition of the Raf kinase pathway (with oral Bay 43-9006) or inhibition of the mTOR pathway (with i.v. CCI-779) are under investigation. Preliminary clinical results with all these compounds are interesting and the results of ongoing phase III studies will become available in the next years.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / therapeutic use*
  • Animals
  • Carcinoma, Renal Cell / epidemiology
  • Carcinoma, Renal Cell / metabolism
  • Carcinoma, Renal Cell / therapy*
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / metabolism
  • Humans
  • Immunotherapy* / methods
  • Immunotherapy* / trends
  • Kidney Neoplasms / epidemiology
  • Kidney Neoplasms / metabolism
  • Kidney Neoplasms / therapy*
  • Neoplasm Metastasis / physiopathology
  • Neoplasm Metastasis / therapy
  • Protein Kinase Inhibitors / therapeutic use*
  • Protein Kinases / metabolism
  • TOR Serine-Threonine Kinases
  • raf Kinases / antagonists & inhibitors
  • raf Kinases / metabolism

Substances

  • Angiogenesis Inhibitors
  • Protein Kinase Inhibitors
  • Protein Kinases
  • MTOR protein, human
  • ErbB Receptors
  • TOR Serine-Threonine Kinases
  • raf Kinases