Population pharmacokinetics of aprepitant and dexamethasone in the prevention of chemotherapy-induced nausea and vomiting

被引:49
作者
Nakade, Susumu [1 ]
Ohno, Tomoya [1 ]
Kitagawa, Junsaku [1 ]
Hashimoto, Yoshitaka [1 ]
Katayama, Masahiro [2 ]
Awata, Hiroshi [2 ]
Kodama, Yasuo [3 ]
Miyata, Yasuyuki [1 ]
机构
[1] Ono Pharmaceut Co Ltd, Pharmacokinet Res Labs, Tsukuba, Ibaraki 3004247, Japan
[2] Ono Pharmaceut Co Ltd, Dev Planning, Osaka, Japan
[3] Josai Int Univ, Fac Pharmaceut Sci, Lab Biopharmaceut, Chiba, Japan
关键词
aprepitant; chemotherapy-induced nausea and vomiting; dexamethasone; population pharmacokinetics;
D O I
10.1007/s00280-008-0713-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To develop a population pharmacokinetic model of aprepitant and dexamethasone in Japanese patients with cancer, explore the factors that affect the pharmacokinetics of aprepitant, and evaluate the effect of aprepitant on the clearance of intravenous dexamethasone. Methods A total of 897 aprepitant concentration measurements were obtained from 290 cancer patients and 25 healthy volunteers. For dexamethasone, a total of 847 measurements were obtained from 440 patients who were co-administered aprepitant (40, 125 mg, or placebo). Plasma concentration of aprepitant and dexamethasone were determined by liquid chromatography connected with a tandem mass spectrometer and analyzed by a population approach using NONMEM software. Results The plasma concentration time course of aprepitant was described using a one-compartment model with first-order absorption and lag time. Oral clearance (CL/F) of aprepitant was changed by aprepitant dose at doses of 40 or 125 mg. Body weight was the most influential intrinsic factor to CL/F of aprepitant. Age, ALT, and BUN also had mild effects on the CL/F. Typical population estimates of CL/F, apparent distribution volume (V-d/F), absorption constant (K-a) and absorption lag time were 1.54 L/h, 72.1 L, 0.893/h and 0.295 h, respectively. Inter-individual variability in CL/F, V (d)/F and K (a) were 53.9, 21.0, and 141%, respectively; intra-individual variability was 27.7%. The plasma concentration time course of intravenous dexamethasone was also described using a one-compartment model. Clearance of dexamethasone was decreased 24.7 and 47.5% by co-administration of aprepitant 40 and 125 mg. All final model estimates of aprepitant and dexamethasone fell within 10% of the bootstrapped mean. Conclusions A pharmacokinetic model for aprepitant has been developed that incorporates body weight, age, ALT, BUN and aprepitant dose to predict the CL/F. The results of population pharmacokinetic analysis of dexamethasone support dose adjustment of dexamethasone in the case of co-administration with aprepitant.
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页码:75 / 83
页数:9
相关论文
共 25 条
[1]  
ARANDA A, 2005, EXPERT REV ANTICANC, V5, P963
[2]  
Beal S., 1989, NONMEM USERS GUIDE
[3]   Effect of impaired renal function and haemodialysis on the pharmacokinetics of aprepitant [J].
Bergman, AJ ;
Marbury, T ;
Fosbinder, T ;
Swan, S ;
Hickey, L ;
Bradstreet, TE ;
Busillo, J ;
Petty, KJ ;
Aiyer, KJV ;
Constanzer, M ;
Huskey, SEW ;
Majumdar, A .
CLINICAL PHARMACOKINETICS, 2005, 44 (06) :637-647
[4]   Effects of aprepitant on the pharmacokinetics of ondansetron and granisetron in healthy subjects [J].
Blum, RA ;
Majumdar, A ;
McCrea, J ;
Busillo, J ;
Orlowski, LH ;
Panebianco, D ;
Hesney, M ;
Petty, KJ ;
Goldberg, MR ;
Murphy, MG ;
Gottesdiener, KM ;
Hustad, CM ;
Lates, C ;
Kraft, WK ;
Van Buren, S ;
Waldman, SA ;
Greenberg, HE .
CLINICAL THERAPEUTICS, 2003, 25 (05) :1407-1419
[5]   Prevention of cisplatin-induced emesis by the oral neurokinin-1 antagonist, MK-869, in combination with granisetron and dexamethasone or with dexamethasone alone [J].
Campos, D ;
Pereira, JR ;
Reinhardt, RR ;
Carracedo, C ;
Poli, S ;
Vogel, C ;
Martinez-Cedillo, J ;
Erazo, A ;
Wittreich, J ;
Eriksson, LO ;
Carides, AD ;
Gertz, BJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1759-1767
[6]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[7]   Determination of a novel substance P inhibitor in human plasma by high-performance liquid chromatography with atmospheric pressure chemical ionization mass spectrometric detection using single and triple quadrupole detectors [J].
Constanzer, ML ;
Chavez-Eng, CM ;
Dru, J ;
Kline, WF ;
Matuszewski, BK .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 807 (02) :243-250
[8]   The oral NK1 antagonist, aprepitant, given with standard antiemetics provides protection against nausea and vomiting over multiple cycles of cisplatin-based chemotherapy:: a combined analysis of two randomised, placebo-controlled phase III clinical trials [J].
de Wit, R ;
Herrstedt, J ;
Rapoport, B ;
Carides, AD ;
Guoguang-Ma, J ;
Elmer, M ;
Schmidt, C ;
Evans, JK ;
Horgan, KJ .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (03) :403-410
[9]   Addition of the oral NK1 antagonist aprepitant to standard antiemetics provides protection against nausea and vomiting during multiple cycles of cisplatin-based chemotherapy [J].
de Wit, R ;
Herrstedt, J ;
Rapoport, B ;
Carides, AD ;
Carides, G ;
Elmer, M ;
Schmidt, C ;
Evans, JK ;
Horgan, KJ .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (22) :4105-4111
[10]   Stability and performance of a population pharmacokinetic model [J].
Ette, EI .
JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 37 (06) :486-495