A phase I study of subcutaneously administered aflibercept (VEGF trap) in a new formulation in patients with advanced solid tumors

被引:5
|
作者
Wang-Gillam, Andrea [1 ]
Tew, William P. [2 ]
Rothenberg, Mace L. [3 ,5 ]
Dupont, Jakob [2 ]
Cooper, Wendy [3 ]
Sternas, Lars [4 ]
Buzenet, Giliane [4 ]
Sosman, Jeffrey A. [3 ]
Spriggs, David R. [2 ]
Lockhart, Albert Craig [1 ]
机构
[1] Washington Univ, Sch Med, St Louis, MO 63110 USA
[2] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[3] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[4] Sanofi Aventis Oncol, Bridgewater, NJ USA
[5] Pfizer Inc, New York, NY USA
关键词
Phase I study; Aflibercept; Angiogenesis inhibitor; Subcutaneously administration; GROWTH-FACTOR-TRAP; ASCITES;
D O I
10.1007/s10637-011-9753-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeting angiogenesis is a valid anti-cancer strategy. Aflibercept is designed to sequester circulating vascular endothelial growth factor (VEGF) by preventing VEGF from binding to its receptors. This phase I study was to evaluate a new formulation of subcutaneously administered aflibercept in patients with advanced solid tumors. Here we report our experience with the toxicity, pharmacokinetic profile and efficacy of the new 100 mg/mL subcutaneous (SC) formulation of aflibercept administered at a dose of at 4 mg/kg every 2 weeks.
引用
收藏
页码:1958 / 1961
页数:4
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