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Effects of Esomeprazole on the Pharmacokinetics of Lapatinib in Breast Cancer Patients.
Koch, Kevin M; Im, Young-Hyuck; Kim, Sung-Bae; Urruticoechea Ribate, Ander; Stephenson, Joe; Botbyl, Jeffrey; Cartee, Leanne; Holshouser, Jane; Ridgway, Derry.
Afiliación
  • Koch KM; GlaxoSmithKline Pharmaceuticals, Clinical Pharmacology Modeling and Simulation, Research Triangle Park, NC, USA.
  • Im YH; Samsung Medical Center, Seoul, Korea.
  • Kim SB; Asan Medical Center.
  • Urruticoechea Ribate A; Institut Catalá d' Oncología, Hospital Duran i Reynals.
  • Stephenson J; Cancer Centers of the Carolinas.
  • Botbyl J; Provonix, LLC.
  • Cartee L; GlaxoSmithKline, Oncology Drug Development.
  • Holshouser J; ICON Clinical Research.
  • Ridgway D; GlaxoSmithKline, Oncology Drug Development.
Clin Pharmacol Drug Dev ; 2(4): 336-41, 2013 Oct.
Article en En | MEDLINE | ID: mdl-27121938
ABSTRACT
The aqueous solubility of lapatinib declines significantly at pH >4, suggesting that its bioavailability might be lowered by acid-reducing drugs. A study was therefore conducted to assess the effects of esomeprazole on lapatinib pharmacokinetics (PK). Women with metastatic human epidermal growth factor receptor 2 positive (HER2(+) ) breast cancer were enrolled. Patients received 1,250 mg lapatinib once daily (QD) in the morning on Days 1-7 (Period 1) and Days 8-14 (Period 2) with 40 mg esomeprazole QD at bedtime 3 hours after dinner on Days 8-14. Lapatinib PK sampling occurred during the 24-hour steady-state dosing intervals on Day 7 (lapatinib alone) and Day 14 (lapatinib with esomeprazole). Esomeprazole treatment resulted in decreased lapatinib bioavailability (mean 26%, range 6-49%) that was inversely associated with patient age as a significant covariate.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Pharmacol Drug Dev Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Clin Pharmacol Drug Dev Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos