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
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 50 条
  • [21] Phase I Study of Cediranib in Combination with Oxaliplatin and Infusional 5-Fluorouracil in Patients with Advanced Colorectal Cancer
    Chen, Eric
    Jonker, Derek
    Gauthier, Isabelle
    MacLean, Martha
    Wells, Julie
    Powers, Jean
    Seymour, Lesley
    CLINICAL CANCER RESEARCH, 2009, 15 (04) : 1481 - 1486
  • [22] Paclitaxel, oxaliplatin, 5-fluorouracil and leucovorin combination chemotherapy in patients with recurrent or metastatic gastric cancer
    Lan, Yan-qin
    Wu, Ri-ping
    Huang, Xiao-bing
    Wang, Xin-li
    Zhong, Dong-ta
    Huang, Chuan-yong
    Song, Jin-tian
    TUMORI JOURNAL, 2018, 104 (01): : 22 - 29
  • [23] Oxaliplatin and protracted venous infusion of 5-fluorouracil in patients with advanced or relapsed 5-fluorouracil pretreated colorectal cancer
    I Chau
    A Webb
    D Cunningham
    M Hill
    J S Waters
    A Norman
    A Massey
    British Journal of Cancer, 2001, 85 : 1258 - 1264
  • [24] Oxaliplatin and protracted venous infusion of 5-fluorouracil in patients with advanced or relapsed 5-fluorouracil pretreated colorectal cancer
    Chau, I
    Webb, A
    Cunningham, D
    Hill, M
    Waters, JS
    Norman, A
    Massey, A
    BRITISH JOURNAL OF CANCER, 2001, 85 (09) : 1258 - 1264
  • [25] A multicenter phase 2 clinical trial testing a combination of oxaliplatin, bolus 5-fluorouracil, leucovorin and capecitabine in patients with metastatic colorectal cancer (MCRC)
    LoConte, N. K.
    Holen, K. D.
    Eickhoff, J.
    Dzelak, T.
    Richie, K.
    Teeter, K.
    Warren, D.
    Jumonville, A. J.
    Kwong, R. W.
    Mulkerin, D. L.
    JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18)
  • [26] Oxaliplatin combined with 5-fluorouracil and methotrexate in advanced colorectal cancer
    Zampino, MG
    Lorizzo, K
    Rocca, A
    Locatelli, M
    Zorzino, L
    Manzoni, S
    Mazzetta, C
    Fazio, N
    Biffi, R
    De Braud, F
    ANTICANCER RESEARCH, 2006, 26 (3B) : 2425 - 2428
  • [27] Systemic treatment options in advanced colorectal cancer: Perspectives on combination 5-fluorouracil plus leucovorin
    Grem, JL
    SEMINARS IN ONCOLOGY, 1997, 24 (05) : 8 - 18
  • [28] A phase I study of vorinostat (suberoylanilide hydroxamic acid, SAHA) in combination with 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) in patients with advanced colorectal cancer (CRC).
    Fakih, M. G.
    Pendyala, L.
    Toth, K.
    Creaven, P.
    Soehnlein, N.
    Litwin, A.
    Trump, D.
    JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (18) : 168S - 168S
  • [30] Phase I study of ursodeoxycholic acid in combination with 5-fluorouracil, leucovorin, oxaliplatin, and bevacizumab for metastatic colorectal cancer
    Lai, Lily L.
    Chiu, Ken
    Lim, Dean
    Chao, Joseph
    Frankel, Paul Henry
    JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (04)