Literature DB >> 26829600

Accurately Achieving Target Busulfan Exposure in Children and Adolescents With Very Limited Sampling and the BestDose Software.

Michael Neely1, Michael Philippe, Teresa Rushing, Xiaowei Fu, Michael van Guilder, David Bayard, Alan Schumitzky, Nathalie Bleyzac, Sylvain Goutelle.   

Abstract

BACKGROUND: Busulfan dose adjustment is routinely guided by plasma concentration monitoring using 4-9 blood samples per dose adjustment, but a pharmacometric Bayesian approach could reduce this sample burden.
METHODS: The authors developed a nonparametric population model with Pmetrics. They used it to simulate optimal initial busulfan dosages, and in a blinded manner, they compared dosage adjustments using the model in the BestDose software to dosage adjustments calculated by noncompartmental estimation of area under the time-concentration curve at a national reference laboratory in a cohort of patients not included in model building.
RESULTS: Mean (range) age of the 53 model-building subjects was 7.8 years (0.2-19.0 years) and weight was 26.5 kg (5.6-78.0 kg), similar to nearly 120 validation subjects. There were 16.7 samples (6-26 samples) per subject to build the model. The BestDose cohort was also diverse: 10.2 years (0.25-18 years) and 46.4 kg (5.2-110.9 kg). Mean bias and imprecision of the 1-compartment model-predicted busulfan concentrations were 0.42% and 9.2%, and were similar in the validation cohorts. Initial dosages to achieve average concentrations of 600-900 ng/mL were 1.1 mg/kg (≤12 kg, 67% in the target range) and 1.0 mg/kg (>12 kg, 76% in the target range). Using all 9 concentrations after dose 1 in the Bayesian estimation of dose requirements, the mean (95% confidence interval) bias of BestDose calculations for the third dose was 0.2% (-2.4% to 2.9%, P = 0.85), compared with the standard noncompartmental method based on 9 concentrations. With 1 optimally timed concentration 15 minutes after the infusion (calculated with the authors' novel MMopt algorithm) bias was -9.2% (-16.7% to -1.5%, P = 0.02). With 2 concentrations at 15 minutes and 4 hours bias was only 1.9% (-0.3% to 4.2%, P = 0.08).
CONCLUSIONS: BestDose accurately calculates busulfan intravenous dosage requirements to achieve target plasma exposures in children up to 18 years of age and 110 kg using only 2 blood samples per adjustment compared with 6-9 samples for standard noncompartmental dose calculations.

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Year:  2016        PMID: 26829600      PMCID: PMC4864122          DOI: 10.1097/FTD.0000000000000276

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  45 in total

1.  Rapid and sensitive high-performance liquid chromatographic method for busulfan assay in plasma.

Authors:  N Bleyzac; P Barou; G Aulagner
Journal:  J Chromatogr B Biomed Sci Appl       Date:  2000-06-09

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4.  Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

Authors:  J E Peris; J A Latorre; V Castel; A Verdeguer; S Esteve; F Torres-Molina
Journal:  J Chromatogr B Biomed Sci Appl       Date:  1999-06-25

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Authors:  R W Jelliffe; A Schumitzky; D Bayard; M Milman; M Van Guilder; X Wang; F Jiang; X Barbaut; P Maire
Journal:  Clin Pharmacokinet       Date:  1998-01       Impact factor: 6.447

6.  Pharmacokinetics of busulfan: correlation with veno-occlusive disease in patients undergoing bone marrow transplantation.

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Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

7.  Development of a rapid and specific assay for detection of busulfan in human plasma by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry.

Authors:  Ederson Oliveira dos Reis; Rosane Vianna-Jorge; Guilherme Suarez-Kurtz; Edson Luiz da Silva Lima; Débora de Almeida Azevedo
Journal:  Rapid Commun Mass Spectrom       Date:  2005       Impact factor: 2.419

8.  Association of busulfan area under the curve with veno-occlusive disease following BMT.

Authors:  S P Dix; J R Wingard; R E Mullins; I Jerkunica; T G Davidson; C E Gilmore; R C York; L S Lin; S M Devine; R B Geller; L T Heffner; C D Hillyer; H K Holland; E F Winton; R Saral
Journal:  Bone Marrow Transplant       Date:  1996-02       Impact factor: 5.483

9.  Graft-rejection and toxicity following bone marrow transplantation in relation to busulfan pharmacokinetics.

Authors:  J T Slattery; J E Sanders; C D Buckner; R L Schaffer; K W Lambert; F P Langer; C Anasetti; W I Bensinger; L D Fisher; F R Appelbaum
Journal:  Bone Marrow Transplant       Date:  1995-07       Impact factor: 5.483

10.  I.V. busulfan in pediatrics: a novel dosing to improve safety/efficacy for hematopoietic progenitor cell transplantation recipients.

Authors:  L Nguyen; D Fuller; S Lennon; F Leger; C Puozzo
Journal:  Bone Marrow Transplant       Date:  2004-05       Impact factor: 5.483

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3.  Prospective Trial on the Use of Trough Concentration versus Area under the Curve To Determine Therapeutic Vancomycin Dosing.

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4.  A Nonparametric Method to Optimize Initial Drug Dosing and Attainment of a Target Exposure Interval: Concepts and Application to Busulfan in Pediatrics.

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7.  Test Dose Pharmacokinetics in Pediatric Patients Receiving Once-Daily IV Busulfan Conditioning for Hematopoietic Stem Cell Transplant: A Reliable Approach?

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Review 8.  Review of the Pharmacokinetics and Pharmacodynamics of Intravenous Busulfan in Paediatric Patients.

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9.  Monitoring of Tobramycin Exposure: What is the Best Estimation Method and Sampling Time for Clinical Practice?

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10.  Population Pharmacokinetic Modeling and Dosing Simulations of Tobramycin in Pediatric Patients with Cystic Fibrosis.

Authors:  Antonin Praet; Laurent Bourguignon; Florence Vetele; Valentine Breant; Charlotte Genestet; Oana Dumitrescu; Anne Doleans-Jordheim; Philippe Reix; Sylvain Goutelle
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