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Plasma 5-fluorouracil and Alpha-fluoro-beta-alanin Accumulation in Lung Cancer Patients Treated with Continuous Infusion of Cisplatin and 5-fluorouracil

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Specialty Oncology
Date 1994 Jan 1
PMID 7987979
Citations 2
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Abstract

This study was undertaken to investigate the day-to-day pharmacokinetic variability of 5-fluorouracil (5FU) given as a continuous i.v. infusion concomitantly with cisplatin. Ten lung cancer patients were investigated during the first course of chemotherapy. All patients had advanced, previously untreated, inoperable non-small-cell lung cancer. They received continuous infusions of cisplatin given at 100 mg/m2 over 5 days and of 5FU given at 1 g/m2 daily from day 2 to day 5. Both drugs were infused i.v. for 24 h/day at a constant rate with a volumetric pump. Blood samples were drawn from day 2 to day 5, every 4 h from 8 a.m. to 8 p.m. and every 2 h during the night (8 p.m. to 8 a.m.). Plasma 5FU and FBAL concentrations were determined simultaneously by gas chromatography-mass spectrometry. Plasma 5FU concentrations varied widely over the 4-day treatment course for each patient. Despite continuous constant-rate 5FU administration, plasma 5FU concentrations were significantly lower between 8 a.m. and 8 p.m. than during the night. Mean plasma concentrations of 5FU and FBAL increased significantly from the 1st day (0.42 and 1.19 micrograms/ml for 5FU and FBAL, respectively) to the 4th day of 5FU infusion (0.67 and 1.78 micrograms/ml for 5FU and FBAL, respectively). Further study is warranted to elucidate the mechanisms of the observed increase in plasma 5FU concentrations as well as its relationship with cisplatin coadministration and to assess the clinical relevance of this plasma 5FU accumulation.

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References
1.
Salem P, Khalyl M, Jabboury K, Hashimi L . Cis-diamminedichloroplatinum (II) by 5-day continuous infusion. A new dose schedule with minimal toxicity. Cancer. 1984; 53(4):837-40. DOI: 10.1002/1097-0142(19840215)53:4<837::aid-cncr2820530403>3.0.co;2-l. View

2.
Fleming R, Milano G, Etienne M, Renee N, Thyss A, Schneider M . No effect of dose, hepatic function, or nutritional status on 5-FU clearance following continuous (5-day), 5-FU infusion. Br J Cancer. 1992; 66(4):668-72. PMC: 1977433. DOI: 10.1038/bjc.1992.335. View

3.
Saltz L, Kelsen D . A phase I trial of cisplatin in hypertonic saline and escalating doses of 5-fluorouracil by continuous intravenous infusion in patients with advanced malignancies. Cancer. 1990; 66(8):1688-91. DOI: 10.1002/1097-0142(19901015)66:8<1688::aid-cncr2820660806>3.0.co;2-k. View

4.
Coustere C, Mentre F, Sommadossi J, Diasio R, Steimer J . A mathematical model of the kinetics of 5-fluorouracil and its metabolites in cancer patients. Cancer Chemother Pharmacol. 1991; 28(2):123-9. DOI: 10.1007/BF00689701. View

5.
Vokes E, Schilsky R, Choi K, Magid D, Guarnieri C, Whaling S . A randomized study of inpatient versus outpatient continuous infusion chemotherapy for patients with locally advanced head and neck cancer. Cancer. 1989; 63(1):30-6. DOI: 10.1002/1097-0142(19890101)63:1<30::aid-cncr2820630105>3.0.co;2-m. View