Factors affecting pharmacokinetic variability following doxorubicin and docetaxel-based therapy

被引:66
作者
Rudek, MA
Sparreboom, A
Garrett-Mayer, ES
Armstrong, DK
Wolff, AC
Verweij, J
Baker, SD
机构
[1] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Div Expt Therapeut, Baltimore, MD 21231 USA
[2] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Div Med Oncol, Baltimore, MD 21231 USA
[3] Erasmus Univ, Med Ctr, Dr Daniel Den Hoed Canc Ctr, Dept Med Oncol, NL-3008 AE Rotterdam, Netherlands
[4] Johns Hopkins, Sidney Kimmel Comprehens Ctr, Div Biostat, Baltimore, MD 21231 USA
关键词
docetaxel; doxorubicin; pharmacokinetics; variability;
D O I
10.1016/j.ejca.2003.12.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Current dosing strategies for anticancer drugs result in wide interindividual pharmacokinetic variability. Here, we explored the influence of age, body size, concomitant drugs, dose, infusion duration, and sex on the clearance for doxorubicin and docetaxel in 243 individual patients. Patients received doxorubicin (n = 110) or docetaxel (n = 152) as monotherapy or in combination chemotherapy regimens. The mean (+/-S.D.) clearance was 63.6 +/- 22.7 L/h for doxorubicin and 42.8 +/- 14.9 L/h for docetaxel. Normalisation for body surface area (BSA) reduced the interindividual variability by only < 1.7%. Doxorubicin clearance was significantly reduced when administered at doses > 50 mg/m(2) or in combination with cyclophosphamide. Upper extremes of body size were associated with increased clearance for both drugs, whereas no consistent effect of age on clearance was discerned. Overall, these findings suggest that incorporation of variables in addition to BSA should be considered in routine dosing strategies for doxorubicin and docetaxel. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1170 / 1178
页数:9
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