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Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure
BACKGROUND: For imatinib, a relationship between systemic exposure and clinical outcome has been suggested. Importantly, imatinib concentrations are not stable and decrease over time, for which several mechanisms have been suggested. In this study, we investigated if a decrease in alpha-1 acid glyco...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315737/ https://www.ncbi.nlm.nih.gov/pubmed/27461250 http://dx.doi.org/10.1007/s40262-016-0441-0 |
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author | Bins, Sander Eechoute, Karel Kloth, Jacqueline S. L. de Man, Femke M. Oosten, Astrid W. de Bruijn, Peter Sleijfer, Stefan Mathijssen, Ron H. J. |
author_facet | Bins, Sander Eechoute, Karel Kloth, Jacqueline S. L. de Man, Femke M. Oosten, Astrid W. de Bruijn, Peter Sleijfer, Stefan Mathijssen, Ron H. J. |
author_sort | Bins, Sander |
collection | PubMed |
description | BACKGROUND: For imatinib, a relationship between systemic exposure and clinical outcome has been suggested. Importantly, imatinib concentrations are not stable and decrease over time, for which several mechanisms have been suggested. In this study, we investigated if a decrease in alpha-1 acid glycoprotein (AGP) is the main cause of the lowering in imatinib exposure over time. METHODS: We prospectively measured imatinib trough concentration (C (min)) values in 28 patients with gastrointestinal stromal tumours, at 1, 3 and 12 months after the start of imatinib treatment. At the same time points, AGP levels were measured. RESULTS: Overall, imatinib C (min) and AGP levels were correlated (r (2) = 0.656; P < 0.001). However, AGP levels did not fluctuate significantly over time, nor did the change in AGP levels correlate with the change in the imatinib C (min). CONCLUSION: We showed that systemic AGP levels are not likely to be a key player in the decrease in systemic imatinib exposure over time. As long as intra-individual changes in imatinib exposure remain unexplained, researchers should standardize the sampling times for imatinib in order to be able to assess the clinical applicability of therapeutic drug monitoring. |
format | Online Article Text |
id | pubmed-5315737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53157372017-03-02 Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure Bins, Sander Eechoute, Karel Kloth, Jacqueline S. L. de Man, Femke M. Oosten, Astrid W. de Bruijn, Peter Sleijfer, Stefan Mathijssen, Ron H. J. Clin Pharmacokinet Short Communication BACKGROUND: For imatinib, a relationship between systemic exposure and clinical outcome has been suggested. Importantly, imatinib concentrations are not stable and decrease over time, for which several mechanisms have been suggested. In this study, we investigated if a decrease in alpha-1 acid glycoprotein (AGP) is the main cause of the lowering in imatinib exposure over time. METHODS: We prospectively measured imatinib trough concentration (C (min)) values in 28 patients with gastrointestinal stromal tumours, at 1, 3 and 12 months after the start of imatinib treatment. At the same time points, AGP levels were measured. RESULTS: Overall, imatinib C (min) and AGP levels were correlated (r (2) = 0.656; P < 0.001). However, AGP levels did not fluctuate significantly over time, nor did the change in AGP levels correlate with the change in the imatinib C (min). CONCLUSION: We showed that systemic AGP levels are not likely to be a key player in the decrease in systemic imatinib exposure over time. As long as intra-individual changes in imatinib exposure remain unexplained, researchers should standardize the sampling times for imatinib in order to be able to assess the clinical applicability of therapeutic drug monitoring. Springer International Publishing 2016-07-26 2017 /pmc/articles/PMC5315737/ /pubmed/27461250 http://dx.doi.org/10.1007/s40262-016-0441-0 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial 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 | Short Communication Bins, Sander Eechoute, Karel Kloth, Jacqueline S. L. de Man, Femke M. Oosten, Astrid W. de Bruijn, Peter Sleijfer, Stefan Mathijssen, Ron H. J. Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title | Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title_full | Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title_fullStr | Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title_full_unstemmed | Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title_short | Prospective Analysis in GIST Patients on the Role of Alpha-1 Acid Glycoprotein in Imatinib Exposure |
title_sort | prospective analysis in gist patients on the role of alpha-1 acid glycoprotein in imatinib exposure |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315737/ https://www.ncbi.nlm.nih.gov/pubmed/27461250 http://dx.doi.org/10.1007/s40262-016-0441-0 |
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