Clinical pharmacokinetics of oxaliplatin and 5-fluorouracil administered in combination with leucovorin in Korean patients with advanced colorectal cancer

被引:0
作者
Hea-Kyoung Cho
Eun-Sook Lee
Jung-Won Lee
Jong-Kook Park
Jin-Hyoung Kang
Kyung-Shik Lee
Chang-Koo Shim
Suk-Jae Chung
Dae-Duk Kim
Hyo-Jeong Kuh
机构
[1] The Catholic University of Korea,Catholic Research Institutes of Medical Science
[2] Schering Korea,Medical and Regulatory Affairs
[3] Seoul National University Bundang Hospital,College of Pharmacy
[4] Seoul National University,undefined
来源
Journal of Cancer Research and Clinical Oncology | 2006年 / 132卷
关键词
Oxaliplatin; 5-Fluorouracil; Pharmacokinetics; Colorectal cancer;
D O I
暂无
中图分类号
学科分类号
摘要
Purpose: Oxaliplatin and 5-fluorouracil (5-FU) act synergistically in colorectal cancer. Here, we evaluated the pharmacokinetics of oxaliplatin and 5-FU administered in combination with leucovorin in Korean advanced colorectal cancer patients. Methods: Nine patients with advanced colorectal cancer were included in this study. The 3-week regimen consisted of oxaliplatin (2-h infusion, 130 mg/m2 on day 1) followed by 5-FU and leucovorin (2-h infusion, 425 and 20 mg/m2, respectively, from day 1 to day 5). Blood samples were taken and platinum concentrations in total plasma, plasma ultrafiltrate, and RBCs were determined. Plasma concentrations of 5-FU were also determined. Results: The Cmax of oxaliplatin was observed at the end of infusion, with mean values of 4.66, 0.84, and 2.69 μg/ml for total plasma, plasma ultrafiltrate, and RBC samples, respectively. Cmax ratios of total/free were significantly higher than those reported in other ethnic groups. An accumulation of platinum was observed in RBCs, but not in total plasma and plasma ultrafiltrate samples. A significant correlation was found between the total body clearance of ultrafiltrable platinum and creatinine clearance. The Cmax of plasma 5-FU ranged from 23.9 to 533.8 ng/ml, indicating large inter-patient pharmacokinetic variations. Conclusions: This study shows that pharmacokinetics of oxaliplatin in Korean patients is comparable with that of other ethic groups, except for the higher Cmax ratios of total/free. The Cmax of 5-FU in plasma showed large variations among patients. Antitumor efficacy in Korean advanced colorectal cancer patients given oxaliplatin and 5-FU should be further evaluated with respect to pharmacokinetic variabilities.
引用
收藏
页码:320 / 326
页数:6
相关论文
共 204 条
[1]  
Anderson D(1997)Simultaneous gas chromatographic–mass spectrophotometric determination of alpha-fluoro-beta-alanine and 5-fluorouracil in plasma J Chromatogr B Biomed Sci Appl 688 87-93
[2]  
Kerr DJ(1998)Oxaliplatin plus 5-fluorouracil: clinical experience in patients with advanced colorectal cancer Semin Oncol 25 32-39
[3]  
Blesing C(1995)Oxaliplatin (L-OHP): global safety in 682 patients Proc Am Soc Clin Oncol 14 A209-1338
[4]  
Seymour LW(2003)Pharmacokinetic study of oxaliplatin iv chronomodulated infusion combined with 5-fluorouracil iv continuous infusion in the treatment of advanced colorectal cancer Farmaco 58 1333-924
[5]  
Bleiberg H(2004)Prevalence of the IVS14 + 1G>A mutation of dihydropyrimidine dehydrogenase gene Cancer Res Treat 36 42-97
[6]  
de Granmont A(2000)Oxaliplatin: a review of its pharmacological properties and clinical efficacy in metastatic colorectal cancer and its potential in other malignancies Drug 60 895-22
[7]  
Brienza S(1998)Co-variables influencing 5-fluorouracil clearance during continuous venous infusion. A NONMEM analysis Eur J Cancer 34 92-899
[8]  
Vignoud J(1998)Pharmacokinetics and safety profile of oxaliplatin Semin Oncol 25 13-1218
[9]  
Itzhaki M(1997)Cumulative pharmacokinetic study of oxaliplatin, administered every three weeks, combined with 5-fluorouracil in colorectal cancer patients Clin Cancer Res 3 891-125
[10]  
Krikorian A(1997)Phase III trail of 5-fluorouracil, folinic acid and with or without oxaliplatin in previously untreated patients with metastatic colorectal cancer Proc Am Soc Clin Oncol Annu Meet 16 A229-201