Literature DB >> 21224369

Therapeutic drug monitoring for the individualization of docetaxel dosing: a randomized pharmacokinetic study.

Frederike K Engels1, Walter J Loos, Jessica M van der Bol, Peter de Bruijn, Ron H J Mathijssen, Jaap Verweij, Ron A A Mathot.   

Abstract

PURPOSE: Docetaxel pharmacokinetic (PK) parameters, notably clearance and exposure (AUC), are characterized by large interindividual variability. The purpose of this study was to evaluate the effect of PK-guided [area under the plasma concentration versus time curve (AUC) targeted], individualized docetaxel dosing on interindividual variability in exposure. EXPERIMENTAL
DESIGN: A limited sampling strategy in combination with a validated population PK model, Bayesian analysis, and a predefined target AUC was used. Fifteen patients were treated for at least 2 courses with body surface area-based docetaxel and 15 with at least 1 course of PK-guided docetaxel dosing.
RESULTS: Interindividual variability (SD of ln AUC) was decreased by 35% (N = 15) after 1 PK-guided course; when all courses were evaluated, variability was decreased by 39% (P = 0.055). PK-guided dosing also decreased the interindividual variability of percentage decrease in white blood cell and absolute neutrophil counts by approximately 50%.
CONCLUSIONS: Further research is required to determine whether the decrease in PK variability can contribute to a reduction in interindividual variability in efficacy and toxicity. ©2011 AACR.

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Year:  2011        PMID: 21224369     DOI: 10.1158/1078-0432.CCR-10-1636

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  17 in total

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Review 9.  Pharmacokinetics, dynamics and toxicity of docetaxel: Why the Japanese dose differs from the Western dose.

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