Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Population pharmacokinetics of imatinib mesylate in patients with chronic‐phase chronic myeloid leukaemia: results of a phase III study

Title: Population pharmacokinetics of imatinib mesylate in patients with chronic‐phase chronic myeloid leukaemia: results of a phase III study
Authors: Schmidli, H.; Peng, B.; Riviere, G‐J.; Capdeville, R.; Hensley, M.; Gathmann, I.; Bolton, A. E.; Racine‐Poon, A.
Source: British Journal of Clinical Pharmacology ; volume 60, issue 1, page 35-44 ; ISSN 0306-5251 1365-2125
Publisher Information: Wiley
Publication Year: 2005
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Aims This study was designed to investigate the biochemical and physiological covariates or comedications that affect the pharmacokinetics of imatinib mesylate in patients with chronic‐phase chronic myeloid leukaemia (CP CML). Methods Pharmacokinetic data were analyzed in 371 patients receiving 400 mg imatinib once daily during a phase III trial of imatinib vs interferon‐alfa plus cytarabine for the treatment of newly diagnosed CP CML. Covariates included age, weight, sex, ethnicity, haemoglobin (Hb) concentration, white blood cell (WBC) count, liver function, and creatinine concentration. Blood samples for imatinib analysis were taken on treatment days 1 and 29. Nonlinear mixed effects modelling was used for the population pharmacokinetic analysis. Results Population mean estimates (95% confidence interval) at day 1 for apparent clearance (CL) and apparent volume of distribution ( V ) of imatinib were 14 (13‐15) l h −1 and 252 (237‐267) l, respectively. Modelling suggested that CL decreased by 4 (3‐5) l h −1 from day 1 to day 29, whereas V remained unchanged. Interindividual variability in CL and V was 32% and 31%, respectively. Weight, Hb, and WBC count demonstrated small effects on CL and V . Doubling body weight or Hb or halving the WBC count was associated with a 12%, 86% and 8% increase in CL, respectively, and a 32%, 60% and 5% increase in V , respectively. Comedications showed no clear effects on imatinib CL. Conclusions Population covariates and coadministered drugs minimally affected imatinib pharmacokinetics in newly diagnosed CP CML patients.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1111/j.1365-2125.2005.02372.x
Availability: https://doi.org/10.1111/j.1365-2125.2005.02372.x; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2125.2005.02372.x; https://bpspubs.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2125.2005.02372.x
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.BF3B5F7C
Database: BASE