Effects of low-fat and high-fat meals on steady-state pharmacokinetics of lapatinib in patients with advanced solid tumours

被引:0
|
作者
Lot A. Devriese
Kevin M. Koch
Marja Mergui-Roelvink
Gemma M. Matthys
Wen Wee Ma
Andre Robidoux
Joe J. Stephenson
Quincy S. C. Chu
Keith W. Orford
Leanne Cartee
Jeff Botbyl
Nikita Arya
Jan H. M. Schellens
机构
[1] The Netherlands Cancer Institute,Division of Experimental Therapy
[2] The Netherlands Cancer Institute,Department of Clinical Pharmacology
[3] GlaxoSmithKline,Medicines Discovery and Development, Research & Development
[4] GlaxoSmithKline,Oncology Global Business, Research & Development
[5] Roswell Park Cancer Institute,Science Faculty, Department of Pharmaceutical Sciences
[6] Centre Hospitalier de l’Université de Montréal-Hotel-Dieu de Montréal,undefined
[7] Greenville Hospital System Institute for Translational Oncology Research,undefined
[8] Cross Cancer Institute,undefined
[9] Provonix,undefined
[10] contractor to GlaxoSmithKline,undefined
[11] Utrecht University,undefined
来源
Investigational New Drugs | 2014年 / 32卷
关键词
Lapatinib ditosylate; Pharmacokinetics; Food-effect; Interaction; Oral chemotherapy; Tyrosine kinase inhibitor;
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摘要
Aim To quantify the effect of food on the systemic exposure of lapatinib at steady state when administered 1 h before and after meals, and to observe the safety and tolerability of lapatinib under these conditions in patients with advanced solid tumours. Methods This was a three-treatment, randomised, three-sequence cross-over study. Lapatinib was administered 1 h after a low- [B] or a high-fat [C] meal and systemic exposure was compared with that obtained following administration 1 h before a low-fat meal [A]. Results In total, 25 patients were included, of whom 12 were evaluable for the pharmacokinetic analysis. Both low-fat and high-fat meals affected lapatinib exposure. Lapatinib AUC0–24 increased following lapatinib administration 1 h after a low-fat meal by 1.80-fold (90 % CI: 1.37–2.37) and after a high-fat meal by 2.61-fold (90 % CI: 1.98–3.43). Lapatinib Cmax increased following lapatinib administration 1 h after a low-fat meal by 1.90-fold (90 % CI: 1.49–2.43) and after a high-fat meal by 2.66-fold (90 % CI: 2.08–3.41). The most commonly occurring treatment-related toxicity was diarrhoea (8/25, 32 % CTCAE grade 1 and 2/25, 8 % grade 2) and one treatment-related grade ≥ 3 event occurred (fatigue grade 3, 4 %). Conclusions Both low-fat and high-fat food consumed 1 h before lapatinib administration increased lapatinib systemic exposure compared with lapatinib administration 1 h before a low-fat meal. In order to administer lapatinib in a fasted state, it is advised to administer the drug 1 h before a meal.
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页码:481 / 488
页数:7
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