Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution

被引:27
作者
Kerr, DJ
Young, AM
Neoptolemos, JP
Sherman, M
VanGeene, P
Stanley, A
Ferry, D
Dobbie, JW
Vincke, B
Gilbert, J
ElEini, D
Dombros, N
Fountzilas, G
机构
[1] QUEEN ELIZABETH HOSP,DEPT SURG,BIRMINGHAM B15 2TH,W MIDLANDS,ENGLAND
[2] CITY HOSP,NHS TRUST,DEPT OBSTET & GYNAECOL,BIRMINGHAM B18 7QH,W MIDLANDS,ENGLAND
[3] AHEPA UNIV HOSP,DEPT INTERNAL MED 1,THESSALONIKI,GREECE
[4] BAXTER R&D EUROPE,NIVELLES,BELGIUM
关键词
intraperitoneal infusion; 5-fluorouracil; icodextrin;
D O I
10.1038/bjc.1996.672
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A novel peritoneal carrier solution, Icodextrin 20 (7.5%), has allowed exploration of prolonged, intraperitoneal (i.p.) infusion of the cytotoxic drug 5-fluorouracil (5-FU). A phase I and pharmacokinetic study was performed to determine the toxicities and maximum tolerated dose of prolonged and continuous intraperitoneal 5-FU in patients with peritoneal carcinomatosis. Seventeen patients were entered into this study. Each patient had a Tenckhoff catheter placed into the peritoneal cavity under general anaesthetic. After initial flushing and gradual increase in exchange volumes with Icodextrin 20, 5-FU was administered daily from Monday to Friday, 50% as a bolus in the exchange bag and 50% in an elastomeric infusor device delivering continuous 5-FU to the peritoneal cavity at 2 ml h(-1). Treatment was continued for 12 weeks or until intolerable toxicity developed. Abdominal pain and infective peritonitis proved to be the main dose-limiting toxicities. Initial problems with infective peritonitis were overcome by redesign of the delivery system, and it proved possible to deliver 300 mg m(-2) 5-FU daily (5 days per week) for 12 weeks. Pharmacokinetic studies showed i.p. steady-state 5-FU concentrations (mean 47 500 ng ml(-1)) that were >1000-fold higher than systemic venous levels (mean 30 ng ml(-1)).
引用
收藏
页码:2032 / 2035
页数:4
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