Gemcitabine increases systemic 5-fluorouracil exposure in advanced cancer patients

被引:19
|
作者
Correale, P
Cerretani, D
Marsili, S
Pozzessere, D
Petrioli, R
Messinese, S
Sabatino, M
Roviello, F
Pinto, E
Francini, G
Giorgi, G
机构
[1] Univ Siena, Sch Med, Dept Human Pathol & Oncol, Sect Oncol, I-53100 Siena, Italy
[2] Univ Siena, Sch Med, Dept Pharmacol Giorgio Segre, I-53100 Siena, Italy
[3] Univ Siena, Sch Med, Dept Human Pathol & Oncol, Sect Surg Oncol, I-53100 Siena, Italy
关键词
gemcitabine; 5-fluorouracil; pharmacokinetics;
D O I
10.1016/S0959-8049(03)00361-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A number of recent clinical trials testing the combination of 5-fluorouracil (5-FU) and gemcitabine in patients with advanced pancreatic adenocarcinoma have shown a significant clinical response rate, but also significant toxicity. As the two antimetabolites may interact at several biochemical levels along their pathways of activation, we investigated whether gemcitabine (GEM) affects 5-FU pharmacokinetics in cancer patients. Thus, we compared 5-FU pharmacokinetics in two groups of patients with various cancers who received the same schedule of 5-FU and folinic acid (FUFA), with or without GEM. There was a significant increase in systemic (5-FU) exposure and toxicity in the FUFA plus GEM group. Our finding may be useful in designing future studies of the combination in order to reduce the occurrence of side-effects and to maximise the antitumour activity. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1547 / 1551
页数:5
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