Development of a pharmacokinetic‐guided dose individualization strategy for hydroxyurea treatment in children with sickle cell anaemia. (5th February 2016)

• Record Type: Journal Article
• Authors: Dong, Min; McGann, Patrick T.; Mizuno, Tomoyuki; Ware, Russell E.; Vinks, Alexander A.
• Is Part Of: British journal of clinical pharmacology. Volume 81:Number 4(2016:Apr.)
• Page Start: 742
• Page End: 752
• Publication Date: 2016-02-05
• Subjects: cystatin C -- hydroxyurea (HU) -- individualized dosing -- maximum tolerated dose (MTD) -- population pharmacokinetics -- sickle cell anaemia (SCA); Pharmacology -- Periodicals; Drugs -- Periodicals; 615.1
• DOI: 10.1111/bcp.12851
• Languages: English
• ISSNs: 0306-5251

Abstract

Abstract : AIMS: Hydroxyurea has emerged as the primary disease‐modifying therapy for patients with sickle cell anaemia (SCA). The laboratory and clinical benefits of hydroxyurea are optimal at maximum tolerated dose (MTD), but the current empirical dose escalation process often takes up to 12 months. The purpose of this study was to develop a pharmacokinetic‐guided dosing strategy to reduce the time required to reach hydroxyurea MTD in children with SCA. Methods: Pharmacokinetic (PK) data from the HUSTLE trial (NCT00305175) were used to develop a population PK model using non‐linear mixed effects modelling (nonmem 7.2). A D‐optimal sampling strategy was developed to estimate individual PK and hydroxyurea exposure (area under the concentration–time curve (AUC)). The initial AUC target was derived from HUSTLE clinical data and defined as the mean AUC at MTD. Results: PK profiles were best described by a one compartment with Michaelis–Menten elimination and a transit absorption model. Body weight and cystatin C were identified as significant predictors of hydroxyurea clearance. The following clinically feasible sampling times are included in a new prospective protocol: pre‐dose (baseline), 15–20 min, 50–60 min and 3 h after an initial 20 mg kg –1 oral dose. The mean target AUC(0, ∞) for initial dose titration was 115 mg l –1 h. Conclusion: We developed a PK model‐based individualized dosing strategy for the prospective Therapeutic Response Evaluation and Adherence Trial (TREAT, ClinicalTrials.gov NCT02286154). This approach has the potential to optimize the dose titration of hydroxyurea therapy for children with SCA, such that the clinical benefits at MTD are achieved more quickly.