Literature DB >> 22011723

Development and validation of limited sampling strategies for estimation of cyclosporine area under the concentration-time curve in hematopoietic stem cell transplant patients.

Molouk Hadjibabaie1, Iman Vazirian, Masoud Iravani, Seyed Asadollah Moosavi, Kamran Alimoghaddam, Ardeshir Ghavamzadeh, Saeed Rezaee.   

Abstract

The aim of this study was to develop and validate limited sampling strategies for accurately predicting 12-hour area under the concentration-time curve (AUC(0-12 h)) to provide a practical method for more precise therapeutic drug monitoring of cyclosporine A in stem cell transplant patients. Steady-state cyclosporine blood concentrations were measured within a dosing interval (12 hours post administration) in 35 allogeneic bone marrow transplant patients receiving 238 mg (±117 mg) twice-daily dose of cyclosporine. Limited sampling strategies were developed by multiple linear regression analysis of relationship between cyclosporine A full AUC(0-12 h) values and different combinations of preselected blood concentrations. Validation of the estimating equations was done by a bootstrap-like cross-validation method. Cross-validation results showed that cyclosporine AUC(0-12 h) could be estimated using either 2 or 3 samples within the first 4 hours after drug administration with good accuracy and precision (absolute prediction error of less than 6.2%). The number of estimated area under the drug concentration-time curves within 15% of observed values was greater than 26 (74%) for models used predose concentration with either c(2h) and c(4h) or both. Most of the previously reported single-sample models showed a systematic error in predicting AUC(0-12 h). Although a statistically significant difference in precision of prediction was seen between 3-sample model using c(0), c(2h), and c(4h) and 2-sample models (c(0), c(2h) or c(0), and c(4h)), such a difference (2%) could not be of clinical importance. Other 2-sample estimating equations (models using c(2h) with either c(6h) or c(10h)) with the same degree of precision appear to be less feasible clinically. Cyclosporine AUC(0-12 h) in bone marrow transplant patients could be estimated using 2 or 3 samples within the first 4 hours after drug administration with good accuracy and precision.

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Year:  2011        PMID: 22011723     DOI: 10.1097/FTD.0b013e318235a5df

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


  4 in total

1.  Population pharmacokinetics and Bayesian estimation of cyclosporine in a Tunisian population of hematopoietic stem cell transplant recipient.

Authors:  Hanene Eljebari; Emna Gaies; Nadia Ben Fradj; Nadia Jebabli; Issam Salouage; Sameh Trabelsi; Mohamed Lakhal; Anis Klouz
Journal:  Eur J Clin Pharmacol       Date:  2012-04-15       Impact factor: 2.953

Review 2.  Pharmacokinetics, Pharmacodynamics and Pharmacogenomics of Immunosuppressants in Allogeneic Haematopoietic Cell Transplantation: Part I.

Authors:  Jeannine S McCune; Meagan J Bemer
Journal:  Clin Pharmacokinet       Date:  2016-05       Impact factor: 6.447

3.  Pharmacokinetic tools for the dose adjustment of ciclosporin in haematopoietic stem cell transplant patients.

Authors:  Jean-Baptiste Woillard; Vincent Lebreton; Michael Neely; Pascal Turlure; Stéphane Girault; Jean Debord; Pierre Marquet; Franck Saint-Marcoux
Journal:  Br J Clin Pharmacol       Date:  2014-10       Impact factor: 4.335

4.  Bayesian approach for the estimation of cyclosporine area under the curve using limited sampling strategies in pediatric hematopoietic stem cell transplantation.

Authors:  Sarem Sarem; Jun Li; Olivier Barriere; Catherine Litalien; Yves Théorêt; Anne-Laure Lapeyraque; Fahima Nekka
Journal:  Theor Biol Med Model       Date:  2014-09-05       Impact factor: 2.432

  4 in total

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