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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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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. |
format | Online Article Text |
id | pubmed-4865545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
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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