The potential of sunitinib as a therapy in ovarian cancer

被引:20
作者
Maggiore, Umberto Leone Roberti
Menada, Mario Valenzano
Venturini, Pier Luigi
Ferrero, Simone [1 ,2 ]
机构
[1] Univ Genoa, San Martino Hosp, I-16132 Genoa, Italy
[2] Natl Inst Canc Res, Dept Obstet & Gynecol, I-16132 Genoa, Italy
关键词
efficacy; ovarian cancer; safety; sunitinib; tolerability; tyrosine kinase inhibitors; PHASE-II TRIAL; TYROSINE KINASE INHIBITOR; PRIMARY PERITONEAL CARCINOMA; PLATINUM-RESISTANT OVARIAN; RECURRENT EPITHELIAL OVARIAN; PEGYLATED LIPOSOMAL DOXORUBICIN; CLEAR-CELL CARCINOMA; ADVANCED SOLID MALIGNANCIES; ENDOTHELIAL GROWTH-FACTOR; ANTITUMOR-ACTIVITY;
D O I
10.1517/13543784.2013.841138
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Sunitinib malate (SU11248; Sutent (R); Pfizer, Inc., New York) is a multi-kinase inhibitor currently approved for use in advanced renal cell carcinoma (RCC), imatinib-resistant/-intolerant gastrointestinal stromal tumours and progressive, well-differentiated pancreatic neuroendocrine tumours in patients with unresectable, locally advanced or metastatic disease. Areas covered: This article describes the mechanism of action and of the pharmacokinetics of sunitinib; further, it summarizes Phase I and II trials on the clinical efficacy, tolerability and safety of this agent in the setting of ovarian cancer (OC) treatment. Expert opinion: On the basis of the current literature, sunitinib has shown modest antitumour activity and acceptable toxicity. Studies investigating the impact of horizontal and vertical combinations should represent a priority of future research. Although clinical Phase II trials on the use of sunitinib in the treatment of OC demonstrated an acceptable profile of AEs, a greater comprehension of the toxicity of this compound is recommended.
引用
收藏
页码:1671 / 1686
页数:16
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