Literature DB >> 11391863

A pharmacological study of the weekday-on/weekend-off oral UFT schedule in colorectal cancer patients.

S Sadahiro1, T Suzuki, T Kameya, H Iwase, T Tajima, H Makuuchi.   

Abstract

PURPOSE: The new weekday-on/weekend-off schedule for oral UFT administration consists of its administration for 5 consecutive days followed by 2 days off the drug. The intratumor 5-FU (5-fluorouracil) concentration has been reported to be correlated to the tumor response in patients treated with intravenous 5-FU. The aim of this study was to investigate the pharmacokinetics during the 2 days off the drug in cancer patients treated with the weekday-on/weekend-off schedule for oral UFT.
METHODS: The subjects were 24 colorectal cancer patients. They were divided into three groups, and were all given UFT, 600 mg/day, for 5 days before surgery. Surgery was performed 2, 24, or 48 h after the final dose of UFT. The 5-FU concentrations in the serum, tumor, and in the normal mucosa were measured.
RESULTS: The serum 5-FU concentrations after the final dose of UFT were: 23 +/- 12 ng/ml (mean +/- SD) at 2 h, 7 +/- 3 ng/ml at 24 h, and 6 +/- 3 ng/ml at 48 h. The intratumor 5-FU concentrations were: 113 +/- 45 ng/g at 2 h, 54 +/- 20 ng/ml at 24 h, and 54 +/- 35 ng/ml at 48 h, and the concentrations in the normal mucosa were: 36 +/- 15 ng/g (mean +/- SD) at 2 h, 17 +/- 6 ng/ml at 24 h, and 18 +/- 6 ng/ml at 48 h after the final dose. While the serum 5-FU concentration decreased to very low levels by 24 h after the final dose of UFT, the intratumor 5-FU concentrations were maintained at more than 50 ng/g at least until 48 h after the final dose. The 5-FU concentrations in the normal mucosa were maintained at about one third of the intratumor concentrations at all time points.
CONCLUSION: Although the weekday-on/weekend-off schedule for UFT administration included intermittent 2-day drug-off periods, this pharmacokinetic study revealed that the 5-FU concentrations in the tumor were maintained at much higher levels than in the serum throughout these periods.

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Year:  2001        PMID: 11391863     DOI: 10.1007/s002800000243

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  5 in total

1.  Feasibility of 5-days-on/2-days-off UFT/leucovorin in post-operative long-term adjuvant chemotherapy for colorectal cancer.

Authors:  Yukihiko Tokunaga; Hirokazu Sasaki
Journal:  Oncol Lett       Date:  2012-02-02       Impact factor: 2.967

2.  Phase 1 study of TAS-102 administered once daily on a 5-day-per-week schedule in patients with solid tumors.

Authors:  Michael J Overman; Gauri Varadhachary; Scott Kopetz; Melanie B Thomas; Masakazu Fukushima; Keizo Kuwata; Akira Mita; Robert A Wolff; Paulo M Hoff; Henry Xiong; James L Abbruzzese
Journal:  Invest New Drugs       Date:  2008-06-05       Impact factor: 3.850

3.  An open, multi-centre, phase II clinical trial to evaluate the efficacy and safety of paclitaxel, UFT, and leucovorin in patients with advanced gastric cancer.

Authors:  Y Chao; C P Li; T Y Chao; W C Su; R K Hsieh; M F Wu; K H Yeh; W Y Kao; L T Chen; A L Cheng
Journal:  Br J Cancer       Date:  2006-06-27       Impact factor: 7.640

4.  Uracil/ftorafur/leucovorin combined with irinotecan (TEGAFIRI) or oxaliplatin (TEGAFOX) as first-line treatment for metastatic colorectal cancer patients: results of randomised phase II study.

Authors:  E Bajetta; M Di Bartolomeo; R Buzzoni; L Mariani; N Zilembo; E Ferrario; S Lo Vullo; E Aitini; L Isa; C Barone; S Jacobelli; E Recaldin; G Pinotti; A Iop
Journal:  Br J Cancer       Date:  2007-01-23       Impact factor: 7.640

Review 5.  Comparative pharmacology of oral fluoropyrimidines: a focus on pharmacokinetics, pharmacodynamics and pharmacomodulation.

Authors:  G Milano; J-M Ferrero; E François
Journal:  Br J Cancer       Date:  2004-08-16       Impact factor: 7.640

  5 in total

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