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A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib

PURPOSE: Cyclosporine A (CsA) and imatinib are both CYP3A4 and P-glycoprotein substrates. Concomitant use after hematopoietic stem cell transplantation (HSCT) for chronic myeloid leukemia (CML) or Philadelphia chromosome-positive (Ph+) acute lymphatic leukemia (ALL) may therefore result in a pharmac...

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Autores principales: Atiq, Ferdows, Broers, Annoek E C, Andrews, Louise M, Doorduijn, Jeanette K, Koch, Birgit C P, Van Gelder, Teun, Versmissen, Jorie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865545/
https://www.ncbi.nlm.nih.gov/pubmed/26965514
http://dx.doi.org/10.1007/s00228-016-2038-9
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author Atiq, Ferdows
Broers, Annoek E C
Andrews, Louise M
Doorduijn, Jeanette K
Koch, Birgit C P
Van Gelder, Teun
Versmissen, Jorie
author_facet Atiq, Ferdows
Broers, Annoek E C
Andrews, Louise M
Doorduijn, Jeanette K
Koch, Birgit C P
Van Gelder, Teun
Versmissen, Jorie
author_sort Atiq, Ferdows
collection PubMed
description PURPOSE: Cyclosporine A (CsA) and imatinib are both CYP3A4 and P-glycoprotein substrates. Concomitant use after hematopoietic stem cell transplantation (HSCT) for chronic myeloid leukemia (CML) or Philadelphia chromosome-positive (Ph+) acute lymphatic leukemia (ALL) may therefore result in a pharmacokinetic interaction. Although case reports and a recent small study in children indeed suggested there is a relevant pharmacokinetic interaction, a larger study in adults is lacking. In this study, we assessed the presence and extent of this interaction in patients with CML or Ph+ ALL undergoing HSCT. METHODS: From a large database containing data of all patients receiving HSCT in our center between 2005 and 2015, we selected 16 patients using this drug combination. The average dose-corrected CsA concentration was calculated before and after initiation of imatinib. RESULTS: The average dose-corrected CsA concentration increased during imatinib use in all patients, on average by 94 % (p < 0.001). Based on measured drug concentrations, the CsA dosage needed to be reduced, on average, by 27 % after initiation of imatinib (p = 0.004). CONCLUSIONS: Imatinib significantly increases CsA concentrations in HSCT patients, putting these patients at increased risk of CsA toxicity. We recommend intensive monitoring of CsA concentrations after initiation of imatinib; a pre-emptive CsA dose reduction of 25 % might be considered.
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spelling pubmed-48655452016-05-25 A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib Atiq, Ferdows Broers, Annoek E C Andrews, Louise M Doorduijn, Jeanette K Koch, Birgit C P Van Gelder, Teun Versmissen, Jorie Eur J Clin Pharmacol Pharmacokinetics and Disposition PURPOSE: Cyclosporine A (CsA) and imatinib are both CYP3A4 and P-glycoprotein substrates. Concomitant use after hematopoietic stem cell transplantation (HSCT) for chronic myeloid leukemia (CML) or Philadelphia chromosome-positive (Ph+) acute lymphatic leukemia (ALL) may therefore result in a pharmacokinetic interaction. Although case reports and a recent small study in children indeed suggested there is a relevant pharmacokinetic interaction, a larger study in adults is lacking. In this study, we assessed the presence and extent of this interaction in patients with CML or Ph+ ALL undergoing HSCT. METHODS: From a large database containing data of all patients receiving HSCT in our center between 2005 and 2015, we selected 16 patients using this drug combination. The average dose-corrected CsA concentration was calculated before and after initiation of imatinib. RESULTS: The average dose-corrected CsA concentration increased during imatinib use in all patients, on average by 94 % (p < 0.001). Based on measured drug concentrations, the CsA dosage needed to be reduced, on average, by 27 % after initiation of imatinib (p = 0.004). CONCLUSIONS: Imatinib significantly increases CsA concentrations in HSCT patients, putting these patients at increased risk of CsA toxicity. We recommend intensive monitoring of CsA concentrations after initiation of imatinib; a pre-emptive CsA dose reduction of 25 % might be considered. Springer Berlin Heidelberg 2016-03-11 2016 /pmc/articles/PMC4865545/ /pubmed/26965514 http://dx.doi.org/10.1007/s00228-016-2038-9 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Pharmacokinetics and Disposition
Atiq, Ferdows
Broers, Annoek E C
Andrews, Louise M
Doorduijn, Jeanette K
Koch, Birgit C P
Van Gelder, Teun
Versmissen, Jorie
A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title_full A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title_fullStr A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title_full_unstemmed A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title_short A clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
title_sort clinically relevant pharmacokinetic interaction between cyclosporine and imatinib
topic Pharmacokinetics and Disposition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4865545/
https://www.ncbi.nlm.nih.gov/pubmed/26965514
http://dx.doi.org/10.1007/s00228-016-2038-9
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