Update on systemic therapies of metastatic renal cell carcinoma

World J Urol. 2010 Jun;28(3):303-9. doi: 10.1007/s00345-010-0519-5. Epub 2010 Feb 24.

Abstract

Purpose: Recent advances in understanding the molecular biology of advanced and metastatic renal cell carcinoma (RCC) have led to the development of several targeted agents that show impressive antitumor efficacy. The integration of these drugs into clinical practice has revolutionized the therapeutic management of RCC.

Methods: We reviewed data on all approved targeted agents in the first-line and second-line setting, as well as, studies involving sequential therapy. Data from phase III trials are discussed, and an optional therapeutic algorithm is presented.

Results: Sunitinib should be used as the first-line treatment of choice for good- and intermediate-risk patients according to Memorial Sloan-Kettering Cancer Center (MSKCC) criteria, whereas temsirolimus is recommended for the poor-risk group. The combination of bevacizumab and INF-alpha can be regarded as an alternative to sunitinib. After cytokine failure, patients should be recommended to sorafenib. Everolimus must be considered after first-line failure of a tyrosine kinase inhibitor (TKI); furthermore, recent evidence suggests sequential use of TKIs before administration of everolimus.

Conclusions: A range of potent drugs are available to patients with metastatic RCC. Treatment decisions should be made carefully taking into consideration that all targeted agents only have a palliative effect with prolongation of life, but do not cure metastatic RCC.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Algorithms
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents / administration & dosage*
  • Benzenesulfonates / administration & dosage
  • Benzenesulfonates / adverse effects
  • Bevacizumab
  • Biopsy, Needle
  • Carcinoma, Renal Cell / drug therapy*
  • Carcinoma, Renal Cell / mortality
  • Carcinoma, Renal Cell / secondary*
  • Clinical Trials, Phase III as Topic
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Delivery Systems
  • Everolimus
  • Female
  • Follow-Up Studies
  • Humans
  • Immunohistochemistry
  • Indoles / administration & dosage
  • Indoles / adverse effects
  • Interferon-alpha / administration & dosage
  • Interferon-alpha / adverse effects
  • Kidney Neoplasms / drug therapy*
  • Kidney Neoplasms / mortality
  • Kidney Neoplasms / pathology*
  • Male
  • Maximum Tolerated Dose
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Niacinamide / analogs & derivatives
  • Phenylurea Compounds
  • Pyridines / administration & dosage
  • Pyridines / adverse effects
  • Pyrroles / administration & dosage
  • Pyrroles / adverse effects
  • Risk Assessment
  • Sirolimus / administration & dosage
  • Sirolimus / adverse effects
  • Sirolimus / analogs & derivatives
  • Sorafenib
  • Sunitinib
  • Survival Analysis

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Benzenesulfonates
  • Indoles
  • Interferon-alpha
  • Phenylurea Compounds
  • Pyridines
  • Pyrroles
  • Niacinamide
  • Bevacizumab
  • Everolimus
  • Sorafenib
  • Sunitinib
  • Sirolimus