[Medical treatment of renal cell carcinoma]

Prog Urol. 2013 Nov;23(15):1225-37. doi: 10.1016/j.purol.2013.09.011. Epub 2013 Oct 21.
[Article in French]

Abstract

Aim: To describe drugs used in renal cell carcinoma.

Method: Pubmed search for efficacy, mode of action and side effects for each molecule. Additional data were searched from the French regulatory agencies websites (HAS and ANSM).

Results: Since 2007, a total of three different therapeutic classes in the management of metastatic renal cell carcinoma are available. These three classes are tyrosine kinase inhibitors with sunitinib and sorafenib, the anti-VEGF antibodies (bevacizumab which is associated with alpha interferon in the treatment of advanced kidney cancer) and mTOR inhibitors with temsirolimus and everolimus. These targeted therapies are a major progress in the treatment of patients with metastatic kidney cancer. The side effects encountered with these molecules are numerous but serious side effects are less than 5% of all reported side effects.

Conclusions: A better understanding of molecular mechanisms has enabled the development of new therapies for the treatment of metastatic renal cell carcinoma. In the future, a personalized approach taking into account the biology of each tumor could be created to provide a more targeted treatment.

Keywords: Anti-VEGF antibodies; Anticorps anti-VEGF; Cancer du rein; Inhibiteur de mTOR; Inhibiteur des tyrosines kinases; MTOR inhibitor; Renal cell carcinoma; Targeted therapy; Thérapie ciblée; Tyrosine kinase inhibitor.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / pharmacology
  • Angiogenesis Inhibitors / therapeutic use
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Antibodies, Monoclonal, Humanized / therapeutic use
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Bevacizumab
  • Carcinoma, Renal Cell / drug therapy*
  • Carcinoma, Renal Cell / pathology
  • Everolimus
  • Humans
  • Immunotherapy
  • Indoles / pharmacology
  • Indoles / therapeutic use
  • Interferon alpha-2
  • Interferon-alpha / pharmacology
  • Interferon-alpha / therapeutic use
  • Interleukin-2 / analogs & derivatives
  • Interleukin-2 / pharmacology
  • Interleukin-2 / therapeutic use
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / pathology
  • Neoplasm Metastasis / drug therapy
  • Niacinamide / analogs & derivatives
  • Niacinamide / pharmacology
  • Niacinamide / therapeutic use
  • Phenylurea Compounds / pharmacology
  • Phenylurea Compounds / therapeutic use
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrroles / pharmacology
  • Pyrroles / therapeutic use
  • Receptors, Vascular Endothelial Growth Factor / antagonists & inhibitors
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use
  • Sirolimus / analogs & derivatives
  • Sirolimus / pharmacology
  • Sirolimus / therapeutic use
  • Societies, Medical
  • Sorafenib
  • Sunitinib
  • Vascular Endothelial Growth Factor A / antagonists & inhibitors

Substances

  • Angiogenesis Inhibitors
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Indoles
  • Interferon alpha-2
  • Interferon-alpha
  • Interleukin-2
  • Phenylurea Compounds
  • Protein Kinase Inhibitors
  • Pyrroles
  • Recombinant Proteins
  • Vascular Endothelial Growth Factor A
  • Niacinamide
  • Bevacizumab
  • temsirolimus
  • Everolimus
  • Sorafenib
  • Receptors, Vascular Endothelial Growth Factor
  • aldesleukin
  • Sunitinib
  • Sirolimus