Cellular, pharmacokinetic, and pharmacodynamic aspects of response to camptothecins: can we improve it? (vol 4, pg 152, 2001)

被引:24
|
作者
Jung, LL
Zamboni, WC
机构
[1] Univ Pittsburgh, Inst Canc, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Pharm, Dept Pharmaceut Sci, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Sch Med, Dept Med, Pittsburgh, PA 15213 USA
关键词
D O I
10.1054/drup.2001.0222
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The camptothecins provide a novel class of effective anticancer agents that exert their action against DNA topoisomerase 1. Members of the camptothecins include topotecan, irinotecan, 9-aminocamptothecin, and 9-nitrocamptothecin, which are analogs of the plant alkaloid 20(S)-camptothecin. These agents vary in their antitumor efficacy and toxicity. Several pharmacokinetic and pharmacodynamic factors including cellular efflux, modulation of topoisomerases I and 11, lactone stability, alterations in metabolism, and drug-drug interactions, influence the antitumor response and toxicity of these agents. Preclinical studies suggest that protracted schedules of administration produce greater antitumor effect than bolus administration. However, the optimal treatment regimens and administration schedules of these agents have yet to be established in clinical studies. (C) 2001 Harcourt Publishers Ltd.
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页码:273 / 288
页数:16
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