Estimation of the area under the concentration-versus-time curve of carboplatin following irinotecan using a limited sampling model

被引:10
作者
Asai, G
Ando, Y
Saka, H
Ando, M
Sugiura, S
Sakai, S
Hasegawa, Y
Shimokata, K
机构
[1] Nagoya Univ, Sch Med, Dept Internal Med 1, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Ekisaikai Hosp, Nagoya, Aichi, Japan
[3] Nagoya First Hosp, Japanese Red Cross, Nagoya, Aichi, Japan
[4] Nagoya Univ, Daiko Med Ctr, Nagoya, Aichi, Japan
关键词
carboplatin; irinotecan; limited sampling model; pharmacokinetics;
D O I
10.1007/s002280050542
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objectives: The aim of this study was to develop limited sampling models for estimating the area under the concentration-versus-time curve (AUC) of carboplatin. Methods: Based on pharmacokinetic analyses of 14 patients who received 300 mg.m(2) of carboplatin over a 90-min infusion following irinotecan, we developed limited sampling models with stepwise multiple linear regression analysis. We validated these models to be unbiased and precise using pharmacokinetic data of a second group of 14 patients. We also compared the observed and the predicted AUC in the patients using Calvert's formula with the patients' renal function. Results: We developed the following models: AUC (mg.ml(-1).min) = 0.784 x C-4 + 1.30 (r(2) = 0.930) and AUC = 0.100 x C-0.25 + 0.597 x C-4 + 0.140 (r(2) = 0.992), where C-0.25 and C-4 denote unbound plasma concentrations (mu g.ml(-1)) of carboplatin at 0.25 h and 4 h after the end of infusion, respectively. These models were validated to be unbiased and precise: a mean prediction error (MPE) with standard deviation (SD) = 2.41 (9.45)% and a root mean squared error (RMSE) = 9.42% for the one-sample model, and MPE with(SD) = 1.22 (5.56)% and RMSE = 5.49% for the two-sample model. We also calculated predicted AUC in the patients using Calvert's formula: MPE with(SD) = -5.87 (21.5)% and RMSE = 21.5%. Conclusions: These estimations were, as expected, more accurate than the prediction using Calvert's formula based on patients' renal function. The result of this study confirmed the idea that the pharmacokinetic parameters derived from limited sampling models would be more suitable for pharmacokinetic analysis of carboplatin than those obtained using Calvert's formula.
引用
收藏
页码:725 / 727
页数:3
相关论文
共 14 条
[1]   Pharmacokinetic study of carboplatin given on a 5-day intravenous schedule [J].
Ando, Y ;
Minami, H ;
Saka, H ;
Ando, M ;
Sugiura, S ;
Sakai, S ;
Shimokata, K .
JAPANESE JOURNAL OF CANCER RESEARCH, 1997, 88 (05) :517-521
[2]   CARBOPLATIN DOSAGE - PROSPECTIVE EVALUATION OF A SIMPLE FORMULA BASED ON RENAL-FUNCTION [J].
CALVERT, AH ;
NEWELL, DR ;
GUMBRELL, LA ;
OREILLY, S ;
BURNELL, M ;
BOXALL, FE ;
SIDDIK, ZH ;
JUDSON, IR ;
GORE, ME ;
WILTSHAW, E .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (11) :1748-1756
[3]   A single sample assay for the estimation of the area under the free carboplatin plasma concentration versus time curve [J].
GhazalAswad, S ;
Calvert, AH ;
Newell, DR .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1996, 37 (05) :429-434
[4]  
HARLAND SJ, 1984, CANCER RES, V44, P1693
[5]   Pharmacokinetics of paclitaxel and carboplat dose-escalating and dose-sequencing study in with non-small-cell long cancer [J].
Huizing, MT ;
Giaccone, G ;
vanWarmerdam, LJC ;
Rosing, H ;
Bakker, PJM ;
Vermorken, JB ;
Postmus, PE ;
vanZandwijk, N ;
Koolen, MGJ ;
Huinink, WWTB ;
vanderVijgh, WJF ;
Bierhorst, FJ ;
Lai, A ;
Dalesio, O ;
Pinedo, HM ;
Veenhof, CHN ;
Beijnen, JH .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :317-329
[6]   Phase I and pharmacologic study of the combination paclitaxel and carboplatin as first-line chemotherapy in stage III and IV ovarian cancer [J].
Huizing, MT ;
vanWarmerdam, LJC ;
Rosing, H ;
Schaefers, MCW ;
Lai, A ;
Helmerhorst, TJM ;
Veenhof, CHN ;
Birkhofer, MJ ;
Rodenhuis, S ;
Beijnen, JH ;
tenBokkelHuinink, WW .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (05) :1953-1964
[7]   PHARMACOKINETICS OF HIGH-DOSE ETOPOSIDE AFTER SHORT-TERM INFUSION [J].
KOHL, P ;
KOPPLER, H ;
SCHMIDT, L ;
FRITSCH, HW ;
HOLZ, J ;
PFLUGER, KH ;
JUNGCLAS, H .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1992, 29 (04) :316-320
[8]   CARBOPLATIN AND ETOPOSIDE PHARMACOKINETICS IN PATIENTS WITH TESTICULAR TERATOMA [J].
NEWELL, DR ;
EELES, RA ;
GUMBRELL, LA ;
BOXALL, FE ;
HORWICH, A ;
CALVERT, AH .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1989, 23 (06) :367-372
[9]  
REECE PA, 1987, CANCER CHEMOTH PHARM, V19, P326
[10]   SOME SUGGESTIONS FOR MEASURING PREDICTIVE PERFORMANCE [J].
SHEINER, LB ;
BEAL, SL .
JOURNAL OF PHARMACOKINETICS AND BIOPHARMACEUTICS, 1981, 9 (04) :503-512