Pharmacokinetics of SN2310, an Injectable Emulsion That Incorporates a New Derivative of SN-38 in Patients with Advanced Solid Tumors

被引:19
作者
Marier, Jean-Francois [3 ]
Pheng, Leng [3 ]
My My Trinh [3 ]
Burris, Howard A., III [2 ]
Jones, Suzanne [2 ]
Anderson, Kirsten [1 ]
Warner, Serina [1 ]
Porubek, David [1 ]
机构
[1] OncoGenex Pharmaceut, Bothell, WA 98021 USA
[2] Sarah Cannon Res Inst, Nashville, TN 37203 USA
[3] Pharsight, Montreal, PQ, Canada
关键词
pharmacokinetics; metabolite; clearance; prodrug; SN2310; SN-38; SN-38G; camptothecin; IRINOTECAN; CAMPTOTHECINS; METABOLISM; CANCER; CPT-11;
D O I
10.1002/jps.22645
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
SN2310 is an injectable emulsion composed of vitamin E, a succinate derivative, as well as 7-ethyl-10-hydroxycamptothecin (SN-38), the active metabolite of irinotecan. Single intravenous doses of 15, 20, 25, and 30mg/m(2) of SN2310 emulsion were administered in a total of 26 patients with advanced solid malignancies. Serial blood samples were collected and concentrations of SN2310, SN-38, and SN-38 glucuronide were assayed. Mean systemic clearance of SN2310 ranged between 1.91 and 2.02L/h/m(2). Peak concentrations of SN-38 were observed at the end of infusion, suggesting a fast metabolic conversion of SN2310 to its active form, SN-38. Mean t(1/2) values of SN-38 across the 20-30 mg/m(2) dose levels (131-199 h) were 33-55-fold longer than those observed for SN2310. The systemic exposure of SN-38 increased in a proportional manner over the dose range studied. SN2310 emulsion displayed an improved safety profile as compared with irinotecan. The most significant safety risk was neutropenia. Considering the rapid formation of SN-38, the proportional increase in exposure levels, and its longer elimination half-life, less frequent dosing of SN2310 emulsion may be considered for the treatment of patients with advanced solid malignancies. (C) 2011 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:4536-4545, 2011
引用
收藏
页码:4536 / 4545
页数:10
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