Plasma and salivary pharmacokinetics of 5-fluorouracil (5-FU) in patients with metastatic colorectal cancer receiving 5-FU bolus plus continuous infusion with high-dose folinic acid

被引:33
作者
Joulia, JM
Pinguet, F
Ychou, M
Duffour, J
Astre, C
Bressolle, F [1 ]
机构
[1] Ctr Reg Lutte Canc, Dept Oncopharmacol, Serv Pharm, F-34298 Montpellier 5, France
[2] Ctr Reg Lutte Canc, Unite Oncol Digest, F-34298 Montpellier, France
[3] Fac Pharm Montpellier, Lab Pharmacocinet, F-34060 Montpellier 2, France
关键词
5-fluorouracil; plasma; parotid saliva; pharmacokinetics; metastatic colorectal cancer;
D O I
10.1016/S0959-8049(98)00318-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The comparative saliva/plasma pharmacokinetics of 5-fluorouracil (5-FU) were investigated in 21 patients with metastatic colorectal cancer receiving high-dose folinic acid (LV (leucovorin) 200 mg/m(2)) followed by 5-FU bolus (400 mg/m(2)) and continuous infusion (600, 750, 900 or 1200 mg/m(2)) on days 1 and 2. Quantitation of unchanged drug was assessed by a highly specific high-performance Liquid chromatographic method. Large patient-to-patient variations in plasma and saliva 5-FU concentrations were observed. Saliva pharmacokinetics could be described using a bi-exponential pattern. The half-life of the rapid phase averaged 8.0 min, and was of the same order of magnitude as the 5-FU elimination half-life determined from plasma data. The half-life of the terminal part of the curve averaged 8 h; such decrease in salivary concentrations could be due to changes in salivary gland function caused by 5-FU, which results in reduced salivary flow rate. Between individual 5-FU concentrations in parotid saliva and plasma a statistically significant straight line could be fitted with a coefficient of correlation of 0.675. Moreover, the risk of developing 5-FU-related mucositis was significantly linked to 5-FU salivary exposure. Diarrhoea was the most frequent toxicity encountered during the trial. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:296 / 301
页数:6
相关论文
共 34 条
[1]  
ARBUCK SG, 1989, CANCER, V63, P1036, DOI 10.1002/1097-0142(19890315)63:6+<1036::AID-CNCR2820631309>3.0.CO
[2]  
2-K
[3]   ORAL COOLING (CRYOTHERAPY), AN EFFECTIVE TREATMENT FOR THE PREVENTION OF 5-FLUOROURACIL-INDUCED STOMATITIS [J].
CASCINU, S ;
FEDELI, A ;
FEDELI, SL ;
CATALANO, G .
ORAL ONCOLOGY-EUROPEAN JOURNAL OF CANCER PART B, 1994, 30B (04) :234-236
[4]   DOXORUBICIN AND 5-FLUOROURACIL PLASMA-CONCENTRATIONS AND DETECTABILITY IN PAROTID-SALIVA [J].
CELIO, LA ;
DIGREGORIO, GJ ;
RUCH, E ;
PACE, J ;
PIRAINO, AJ .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1983, 24 (02) :261-266
[5]   NON-LINEAR PHARMACOKINETIC MODELS FOR 5-FLUOROURACIL IN MAN - INTRAVENOUS AND INTRAPERITONEAL ROUTES [J].
COLLINS, JM ;
DEDRICK, RL ;
KING, FG ;
SPEYER, JL ;
MYERS, CE .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1980, 28 (02) :235-246
[6]   HIGH-DOSE FOLINIC ACID AND 5-FLUOROURACIL BOLUS AND CONTINUOUS INFUSION IN ADVANCED COLORECTAL-CANCER [J].
DEGRAMONT, A ;
KRULIK, M ;
CADY, J ;
LAGADEC, B ;
MAISANI, JE ;
LOISEAU, JP ;
GRANGE, JD ;
GONZALEZCANALL, G ;
DEMUYNCK, B ;
LOUVET, C ;
SEROKA, J ;
DRAY, C ;
DEBRAY, J .
EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1988, 24 (09) :1499-1503
[7]  
DEGRAMONT A, 1995, P ASCO, V14, pA455
[8]  
DUFFOUR J, 1998, P 8 WORLD C INT GAST
[9]  
ERLICHMAN C, 1986, CANCER TREAT REP, V70, P903
[10]  
Gamelin EC, 1996, CANCER, V77, P441, DOI 10.1002/(SICI)1097-0142(19960201)77:3<441::AID-CNCR4>3.0.CO