Sunitinib malate for the treatment of solid tumours: a review of current clinical data

被引:96
作者
Motzer, Robert J.
Hoosen, Sakina
Bello, Carlo L.
Christensen, James G.
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[2] Pfizer Inc, New York, NY 10017 USA
[3] Pfizer Global Res & Dev, San Diego, CA 92121 USA
关键词
antiangiogenic; antitumour; GIST; multitargeted tyrosine kinase inhibitor; RCC; solid tumours; SU11248; sunitinib;
D O I
10.1517/13543784.15.5.553
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Receptor tyrosine kinases (RTKs) play important roles in the regulation of cellular growth, and mutated or overexpressed RTKs have been implicated in various human cancers. Sunitinib malate is an oral multitargeted tyrosine kinase inhibitor with antitumour and antiangiogenic activity that recently received approval from the FDA for the treatment of advanced renal cell carcinoma and of gastrointestinal stromal tumours after disease progression on or intolerance to imatinib mesilate therapy. Sunitinib has also demonstrated promising clinical activity in the treatment of other advanced solid tumours. The present review provides an updated summary of emerging clinical experience with this promising new anticancer agent.
引用
收藏
页码:553 / 561
页数:9
相关论文
共 55 条
[1]  
Abrams TJ, 2003, MOL CANCER THER, V2, P1011
[2]   Effect of food on the pharmacokinetics of sunitinib malate (SU11248), a multi-targeted receptor tyrosine kinase inhibitor: results from a phase I study in healthy subjects [J].
Bello, Carlo L. ;
Sherman, Laurie ;
Zhou, Jihao ;
Verkh, Lev ;
Smeraglia, John ;
Mount, Janessa ;
Klamerus, Karen J. .
ANTI-CANCER DRUGS, 2006, 17 (03) :353-358
[3]   The role of pericytes in blood-vessel formation and maintenance [J].
Bergers, G ;
Song, S .
NEURO-ONCOLOGY, 2005, 7 (04) :452-464
[4]   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
[5]   State-of-the art therapy for gastrointestinal stromal tumors [J].
Blanke, CD ;
Corless, CL .
CANCER INVESTIGATION, 2005, 23 (03) :274-280
[6]   EXPRESSION OF GROWTH-FACTOR PEPTIDES AND THEIR RECEPTORS IN NEUROENDOCRINE TUMORS OF THE DIGESTIVE-SYSTEM [J].
CHAUDHRY, A ;
FUNA, K ;
OBERG, K .
ACTA ONCOLOGICA, 1993, 32 (02) :107-114
[7]   Rising incidence of renal cell cancer in the United States [J].
Chow, WH ;
Devesa, SS ;
Warren, JL ;
Fraumeni, JF .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (17) :1628-1631
[8]   VASCULAR ENDOTHELIAL GROWTH-FACTOR AND ITS RECEPTORS, FLT-1 AND FLK-1, ARE EXPRESSED IN NORMAL PANCREATIC-ISLETS AND THROUGHOUT ISLET-CELL TUMORIGENESIS [J].
CHRISTOFORI, G ;
NAIK, P ;
HANAHAN, D .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (12) :1760-1770
[9]   PDGFRA mutations in gastrointestinal stromal tumors: Frequency, spectrum and in vitro sensitivity to imatinib [J].
Corless, CL ;
Schroeder, A ;
Griffith, D ;
Town, A ;
McGreevey, L ;
Harrell, P ;
Shiraga, S ;
Bainbridge, T ;
Morich, J ;
Heinrich, MC .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (23) :5357-5364
[10]   Biology of gastrointestinal stromal tumors [J].
Corless, CL ;
Fletcher, JA ;
Heinrich, MC .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (18) :3813-3825