Renal-Cell Carcinoma — Molecular Pathways and Therapies
Top Cited Papers
- 11 January 2007
- journal article
- editorial
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 356 (2) , 185-187
- https://doi.org/10.1056/nejme068263
Abstract
Renal-cell carcinoma is among the most resistant of tumors to therapy. Until 2005, only a single treatment, high-dose interleukin-2, had been approved by the Food and Drug Administration (FDA) for the treatment of this disease. The approval was based on durable complete responses in 5% of patients with metastatic disease,1 but high-dose therapy with interleukin-2 is quite toxic, and in most patients its benefit is unclear.In this issue of the Journal, Motzer et al.2 and Escudier et al.3 report on the results of phase 3 trials of two oral, small-molecule kinase inhibitors, sunitinib malate and sorafenib, respectively. Both drugs . . .Keywords
This publication has 12 references indexed in Scilit:
- Sunitinib versus Interferon Alfa in Metastatic Renal-Cell CarcinomaNew England Journal of Medicine, 2007
- Sorafenib in Advanced Clear-Cell Renal-Cell CarcinomaNew England Journal of Medicine, 2007
- A small molecule–kinase interaction map for clinical kinase inhibitorsNature Biotechnology, 2005
- The Von Hippel-Lindau Tumor Suppressor Gene and Kidney CancerClinical Cancer Research, 2004
- mTOR inhibition reverses Akt-dependent prostate intraepithelial neoplasia through regulation of apoptotic and HIF-1-dependent pathwaysNature Medicine, 2004
- Inhibition of HIF2α Is Sufficient to Suppress pVHL-Defective Tumor GrowthPLoS Biology, 2003
- TSC2 regulates VEGF through mTOR-dependent and -independent pathwaysCancer Cell, 2003
- A Randomized Trial of Bevacizumab, an Anti–Vascular Endothelial Growth Factor Antibody, for Metastatic Renal CancerNew England Journal of Medicine, 2003
- Regulation of Hypoxia-Inducible Factor 1α Expression and Function by the Mammalian Target of RapamycinMolecular and Cellular Biology, 2002
- Results of treatment of 255 patients with metastatic renal cell carcinoma who received high-dose recombinant interleukin-2 therapy.Journal of Clinical Oncology, 1995