Randomized pharmacokinetic and pharmacodynamic study of docetaxel: Dosing based on body-surface area compared with individualized dosing based on cytochrome P450 activity estimated using a urinary metabolite of exogenous cortisol

被引:77
作者
Yamamoto, N
Tamura, T
Murakami, H
Shimoyama, T
Nokihara, H
Ueda, Y
Sekine, I
Kunitoh, H
Ohe, Y
Kodama, T
Shimizu, M
Nishio, K
Ishizuka, N
Saijo, N
机构
[1] Natl Canc Ctr, Div Internal Med, Chuo Ku, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Res Inst, Div Pharmacol, Tokyo 104, Japan
[3] Natl Canc Ctr, Res Inst, Informat & Epidemiol Div, Tokyo 104, Japan
关键词
D O I
10.1200/JCO.2005.11.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Docetaxel is metabolized by cytochrome P450 (CYP3A4) enzyme, and the area under the concentration-time curve (AUC) is correlated with neutropenia. We developed a novel method for estimating the interpatient variability of CYP3A4 activity by the urinary metabolite of exogenous cortisol (6-beta-hydroxycortisol 16-beta-OHF]). This study was designed to assess whether the application of our method to individualized dosing could decrease pharmacokinetic (PK) and pharmacodynamic (PD) variability compared with body-surface area (BSA)-based dosing. Patients and Methods Fifty-nine patients with advanced non-small-cell lung cancer were randomly assigned to either the BSA-based arm or individualized arm. In the BSA-based arm, 60 mg/m(2) of docetaxel was administered. In the individualized arm, individualized doses of docetaxel were calculated from the estimated clearance (estimated clearance = 31.177 + [7.655 X 10(-4) X total 6-beta-OHF] - [4.02 X alpha-1 acid glycoprotein] - [0.172 x AST] - [0.125 X age]) and the target AUC of 2.66 mg/L (.) h. Results In the individualized arm, individualized doses of docetaxel ranged from 37.4 to 76.4 mg/m(2) (mean, 58.1 mg/m(2)). The mean AUC and standard deviation (SD) were 2.71 (range, 2.02 to 3.40mg/L(.)h)and 0.40mg/L (.) h in the BSA-based arm, and 2.64 (range, 2.15 to 3.07 mg/L (.) h) and 0.22 mg/L (.) h in the individualized arm, respectively. The SD of the AUC was significantly smaller in the individualized arm than in the BSA-based arm (P < .01). The percentage decrease in absolute neutrophil count (ANC) averaged 87.1% (range, 59.0 to 97.7%; SD, 8.7) in the BSA-based arm, and 87.4% (range, 78.0 to 97.2%; SD, 6.1) in the individualized arm, suggesting that the interpatient variability in percent decrease in ANC was slightly smaller in the individualized arm. Conclusion The individualized dosing method based on the total amount of urinary 6-beta-OHF after cortisol administration can decrease PK variability of docetaxel. (C) 2005 by American Society of Clinical Oncology.
引用
收藏
页码:1061 / 1069
页数:9
相关论文
共 43 条
[31]   Body-surface area as a basis for dosing of anticancer agents: Science, myth, or habit? [J].
Ratain, MJ .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (07) :2297-2298
[32]   STUDIES WITH RP-56976 (TAXOTERE) - A SEMISYNTHETIC ANALOG OF TAXOL [J].
RINGEL, I ;
HORWITZ, SB .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (04) :288-291
[33]   Body surface area as a determinant of pharmacokinetics and drug dosing [J].
Sawyer, M ;
Ratain, MJ .
INVESTIGATIONAL NEW DRUGS, 2001, 19 (02) :171-177
[34]   Prospective randomized trial of docetaxel versus best supportive care in patients with non-small-cell lung cancer previously treated with platinum-based chemotherapy [J].
Shepherd, FA ;
Dancey, J ;
Ramlau, R ;
Mattson, K ;
Gralla, R ;
O'Rourke, M ;
Levitan, N ;
Gressot, L ;
Vincent, M ;
Burkes, R ;
Coughlin, S ;
Kim, Y ;
Berille, J .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (10) :2095-2103
[35]  
SHIMADA T, 1994, J PHARMACOL EXP THER, V270, P414
[36]  
Taguchi T, 1994, Gan To Kagaku Ryoho, V21, P2453
[37]  
THUMMEL KE, 1994, J PHARMACOL EXP THER, V271, P557
[38]  
THUMMEL KE, 1994, J PHARMACOL EXP THER, V271, P549
[39]   Docetaxel in patients with metastatic breast cancer: A phase II study of the National Cancer Institute of Canada - Clinical Trials Group [J].
Trudeau, ME ;
Eisenhauer, EA ;
Higgins, BP ;
Letendre, F ;
Lofters, WS ;
Norris, BD ;
Vandenberg, TA ;
Delorme, F ;
Muldal, AM .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (02) :422-428
[40]   DETERMINATION OF TAXOTERE IN HUMAN PLASMA BY A SEMIAUTOMATED HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC METHOD [J].
VERGNIOL, JC ;
BRUNO, R ;
MONTAY, G ;
FRYDMAN, A .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1992, 582 (1-2) :273-278