Treatment options in renal cell carcinoma: past, present and future

被引:55
作者
Oudard, S.
George, D.
Medioni, J.
Motzer, R.
机构
[1] Hop Europeen Georges Pompidou, Serv Cancerol Med, F-75908 Paris 15, France
[2] Duke Univ, Med Ctr, Durham, NC USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
关键词
receptor tyrosine kinase inhibitor; renal cell carcinoma; sorafenib; sunitinib; temsirolimus;
D O I
10.1093/annonc/mdm411
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytokine therapies have been the standard of care in metastatic renal cell carcinoma (RCC). However, these agents only provide clinical benefit to a small subset of patients and are associated with significant toxicity. A better understanding of the molecular biology of RCC has identified the vascular endothelial growth factor (VEGF) and platelet-derived growth factor signalling pathways as rational targets for anticancer therapy. The multitargeted receptor tyrosine kinase inhibitors sunitinib and sorafenib have both demonstrated improved efficacy as second-line therapy in patients with RCC. Sunitinib has also been shown to be effective in the first-line setting, and has recently received European Union approval as first-line treatment for advanced and/or metastatic RCC. There is also recent evidence that temsirolimus (an inhibitor of the mammalian target of rapamycin) and bevacizumab (a mAb targeted against VEGF) may provide benefits in the first-line treatment setting. These results confirm that inhibiting these tumour targets is a feasible approach to treatment and provides a more positive outlook for the future management of metastatic RCC.
引用
收藏
页码:25 / 31
页数:7
相关论文
共 48 条
[1]  
Abrams TJ, 2003, MOL CANCER THER, V2, P1011
[2]  
[Anonymous], J CLIN ONCOL S
[3]   Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell carcinoma [J].
Atkins, MB ;
Hidalgo, M ;
Stadler, WM ;
Logan, TF ;
Dutcher, JP ;
Hudes, GR ;
Park, Y ;
Lion, SH ;
Marshall, B ;
Boni, JP ;
Dukart, G ;
Sherman, ML .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (05) :909-918
[4]   Adjuvant treatment with interleukin-2-and interferon-alpha2a-based chemoimmunotherapy in renal cell carcinoma post tumour nephrectomy:: Results of a prospectively randomised Trial of the German Cooperative Renal Carcinoma Chemoimmunotherapy Group (DGCIN) [J].
Atzpodien, J ;
Schmitt, E ;
Gertenbach, U ;
Fornara, P ;
Heynemann, H ;
Maskow, A ;
Ecke, M ;
Wöltjen, HH ;
Jentsch, H ;
Wieland, W ;
Wandert, T ;
Reitz, M .
BRITISH JOURNAL OF CANCER, 2005, 92 (05) :843-846
[5]   Benefits of targeting both pericytes and endothelial cells in the tumor vasculature with kinase inhibitors [J].
Bergers, G ;
Song, S ;
Meyer-Morse, N ;
Bergsland, E ;
Hanahan, D .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (09) :1287-1295
[6]  
Bukowski RM, 2006, ANN ONCOL, V17, P144
[7]  
Chan D Y, 1998, Curr Opin Urol, V8, P369, DOI 10.1097/00042307-199809000-00002
[8]   Adjuvant high-dose bolus interleukin-2 for patients with high-risk renal cell carcinoma: A cytokine working group randomized trial [J].
Clark, JI ;
Atkins, MB ;
Urba, WJ ;
Creech, S ;
Figlin, RA ;
Dutcher, JP ;
Flaherty, L ;
Sosman, JA ;
Logan, TF ;
White, R ;
Weiss, GR ;
Redman, BG ;
Tretter, CPG ;
McDermott, D ;
Smith, JW ;
Gordon, MS ;
Margolin, KA .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (16) :3133-3140
[9]   RETRACTED: Immunotherapy for advanced renal cell cancer - art. no. CD001425.pub2 (Retracted Article) [J].
Coppin, C ;
Porzsolt, F ;
Awa, A ;
Kumpf, J ;
Coldman, A ;
Wilt, T .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2005, (01)
[10]   Combined inhibition of VEGF- and PDGF-signaling enforces tumor vessel regression by interfering with pericyte-mediated endothelial cell survival mechanisms [J].
Erber, R ;
Thurnher, A ;
Katsen, AD ;
Groth, G ;
Kerger, H ;
Hammes, HP ;
Menger, MD ;
Ullrich, A ;
Vajkoczy, P .
FASEB JOURNAL, 2003, 17 (15) :338-340