Effect of food on the pharmacokinetics of erlotinib, an orally active epidermal growth factor receptor tyrosine-kinase inhibitor, in healthy individuals

被引:71
作者
Ling, Jie [1 ]
Fettner, Scott [2 ]
Lum, Bert L. [1 ]
Riek, Myriam [3 ]
Rakhit, Ashok [2 ]
机构
[1] Genentech Inc, San Francisco, CA 94080 USA
[2] F Hoffmann La Roche Inc, Dept Clin Pharmacol, Nutley, NJ USA
[3] F Hoffmann La Roche & Co Ltd, Dept Global Drug Dev Biostat, CH-4002 Basel, Switzerland
关键词
erlotinib; food effect; pharmacokinetics; CELL LUNG-CANCER; CLINICAL PHARMACOKINETICS; DRUG ABSORPTION; OSI-774; BIOAVAILABILITY; HYDROCHLORIDE; CHEMOTHERAPY; COMBINATION; RECURRENT; TARCEVA;
D O I
10.1097/CAD.0b013e3282f2d8e4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effects of food on the pharmacokinetics of erlotinib were investigated in two open-label, randomized studies. In a single-dose crossover study (n = 18), 150 mg of erlotinib was administered under either fasting or fed conditions. In the first period, an approximate doubling in the area under the plasma concentration-time curve was evidenced by the geometric mean ratio (GMR) of 2.09 observed under fed conditions; whereas, in the second period there was a decrease, with a GMR of 0.93. In a multiple-dose parallel study (n=22), 100 mg of erlotinib was administered daily for 8 days, either 7 days of fasting followed by feeding on day 8, or the reverse sequence. In this study, food resulted in an increase in the plasma concentration-time curve on day 1, with a GMR of 1.66 (P=0.015). In contrast, there was only a 37% increase on day 7, with a GMR of 1.34 (P=0.252). These studies indicate that food can substantially increase plasma exposure to erlotinib. Given the maximum tolerated dose of erlotinib used in clinical practice, we recommend that erlotinib be taken under conditions of fasting.
引用
收藏
页码:209 / 216
页数:8
相关论文
共 21 条
[1]  
[Anonymous], 2003, Design and analysis of crossover trials
[2]  
[Anonymous], PRESCRIBING INFORM
[3]   THE EFFECT OF FOOD ON THE RELATIVE BIOAVAILABILITY OF FADROZOLE HYDROCHLORIDE [J].
CHOI, RL ;
SUN, JX ;
KOCHAK, GM .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1993, 14 (09) :779-784
[4]  
Chow SC., 2000, Design and analysis of bioavailability and bioequivalence studies, V2nd
[5]   Drug, meal and formulation interactions influencing drug absorption after oral administration - Clinical implications [J].
Fleisher, D ;
Li, C ;
Zhou, Y ;
Pao, LH ;
Karim, A .
CLINICAL PHARMACOKINETICS, 1999, 36 (03) :233-254
[6]   Evaluation of the absolute oral bioavailability and bioequivalence of erlotinib, an inhibitor of the epidermal growth factor receptor tyrosine kinase, in a randomized, crossover study in healthy subjects [J].
Frohna, P ;
Lu, JF ;
Eppler, S ;
Hamilton, M ;
Wolf, J ;
Rakhit, A ;
Ling, J ;
Kenkare-Mitra, SR ;
Lum, BL .
JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 46 (03) :282-290
[7]   Phase I/II trial evaluating the anti-vascular endothelial growth factor monoclonal antibody bevacizumab in combination with the HER-1/epidermal growth factor receptor tyrosine kinase inhibitor erlotinib for patients with recurrent non-small-cell lung cancer [J].
Herbst, RS ;
Johnson, DH ;
Mininberg, E ;
Carbone, DP ;
Henderson, T ;
Kim, ES ;
Blumenschein, G ;
Lee, JJ ;
Liu, DD ;
Truong, MT ;
Hong, WK ;
Tran, H ;
Tsao, A ;
Xie, D ;
Ramies, DA ;
Mass, R ;
Seshagiri, S ;
Eberhard, DA ;
Kelley, SK ;
Sandler, A .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2544-2555
[8]   TRIBUTE: A phase III trial of erlotinib hydrochloride (OSI-774) combined with carboplatin and paclitaxel chemotherapy in advanced non-small-cell lung cancer [J].
Herbst, RS ;
Prager, D ;
Hermann, R ;
Fehrenbacher, L ;
Johnson, BE ;
Sandler, A ;
Kris, MG ;
Tran, HT ;
Klein, P ;
Li, X ;
Ramies, D ;
Johnson, DH ;
Miller, VA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :5892-5899
[9]   Phase I and pharmacologic study of OSI-774, an epidermal growth factor receptor tyrosine kinase inhibitor, in patients with advanced solid malignancies [J].
Hidalgo, M ;
Siu, LL ;
Nemunaitis, J ;
Rizzo, J ;
Hammond, LA ;
Takimoto, C ;
Eckhardt, SG ;
Tolcher, A ;
Britten, CD ;
Denis, L ;
Ferrante, K ;
Von Hoff, DD ;
Silberman, S ;
Rowinsky, EK .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (13) :3267-3279
[10]   Antitumor activity of erlotinib (OSI-774, Tarceva) alone or in combination in human non-small cell lung cancer tumor xenograft models [J].
Higgins, B ;
Kolinsky, K ;
Smith, M ;
Beck, G ;
Rashed, M ;
Adames, V ;
Linn, M ;
Wheeldon, E ;
Gand, L ;
Birnboeck, H ;
Hoffmann, G .
ANTI-CANCER DRUGS, 2004, 15 (05) :503-512