Literature DB >> 6224555

Phase I study of continuous venous infusion of floxuridine (5-FUDR) chemotherapy.

J J Lokich, H Sonneborn, S Paul, T Zipoli.   

Abstract

Floxuridine (5-FUDR) was administered by continuous venous infusion using an ambulatory portable pump in a phase I study designed to establish the optimal (maximal) daily dose rate to deliver a minimum of 14 days of drug therapy. The major determinant of toxicity was dose rate rather than cumulative dose. Patients receiving greater than 0.15 mg/kg/day developed dose-limiting diarrhea at 7-14 days (median, 10), while patients receiving 0.1-0.125 mg/kg/day were treated for 18-78 days without adverse effects. The recommended daily dose rate for continuous-infusion schedules of 14 days is 0.15 mg/kg/day.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6224555

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  2 in total

Review 1.  Continuous infusion of chemotherapy: focus on 5-fluorouracil and fluorodeoxyuridine.

Authors:  R L Poorter; P J Bakker; C H Veenhof
Journal:  Pharm World Sci       Date:  1998-04

2.  Phase I and pharmacokinetic evaluation of floxuridine/leucovorin given on the Roswell Park weekly regimen.

Authors:  P J Creaven; Y M Rustum; N J Petrelli; N J Meropol; D Raghavan; M Rodriguez-Bigas; E G Levine; C Frank; S Udvary-Nagy; A Proefrock
Journal:  Cancer Chemother Pharmacol       Date:  1994       Impact factor: 3.333

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.