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Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma

In view of the antineoplastic effects of the macrolide clarithromycin in mucosa associated lymphatic tissue (MALT)-lymphoma, we performed a pilot study assessing levels of azithromycin in plasma, peripheral blood mononuclear cells (PBMC) and polymorphonuclear leukocytes (PMN) of MALT-lymphoma patien...

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Autores principales: Scheibenpflug, Raphael, Obermüller, Markus, Reznicek, Gottfried, Neuper, Ortrun, Lamm, Wolfgang W., Raderer, Markus, Lagler, Heimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445944/
https://www.ncbi.nlm.nih.gov/pubmed/34531427
http://dx.doi.org/10.1038/s41598-021-97836-w
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author Scheibenpflug, Raphael
Obermüller, Markus
Reznicek, Gottfried
Neuper, Ortrun
Lamm, Wolfgang W.
Raderer, Markus
Lagler, Heimo
author_facet Scheibenpflug, Raphael
Obermüller, Markus
Reznicek, Gottfried
Neuper, Ortrun
Lamm, Wolfgang W.
Raderer, Markus
Lagler, Heimo
author_sort Scheibenpflug, Raphael
collection PubMed
description In view of the antineoplastic effects of the macrolide clarithromycin in mucosa associated lymphatic tissue (MALT)-lymphoma, we performed a pilot study assessing levels of azithromycin in plasma, peripheral blood mononuclear cells (PBMC) and polymorphonuclear leukocytes (PMN) of MALT-lymphoma patients to determine the pharmacokinetics and potential influences of respective concentrations on the therapeutic outcome. In total 16 patients with MALT-lymphoma received 1.5 g of oral azithromycin once-weekly over 6 months. Blood was sampled directly prior to the following dose every 4 weeks during treatment. Drug levels were analysed by high performance liquid chromatography in plasma and intracellularly in PBMC and PMN. They were correlated with patients’ age, weight and body-mass-index and compared between patients responsive or unresponsive to treatment. Mean azithromycin plasma levels of all patients were 58.97 ± 30.48 ng/ml, remaining stable throughout the treatment period. Correlation analysis of plasma azithromycin showed no significance. Intracellular PBMC concentrations were 6648 ± 8479 ng/ml, without any significant difference between responders and non-responders. Mean PMN levels were 39,274 ± 25,659 ng/ml and significantly higher in patients unresponsive to treatment (t = 2.858, p = 0.017). Our drug regime led to continuously high plasma and exceedingly high intracellular concentrations of azithromycin in PBMC and PMN. Age, weight or body-mass-index had no significant influence on plasma levels and thence should not be considered in dosage finding. High AZM levels in PBMC did not lead to a better treatment response, whereas enrichment in PMN suggested a poorer outcome. The threshold for immunomodulatory effects on lymphoma cells might not have been reached. Additionally, the finding of stable plasma and intracellular concentrations over months with high-dose azithromycin administered in intervals might also be important for the further design of azithromycin-based trials against MALT-lymphoma. Trial registration: EudraCT 2016-001521-13, 14/06/2016.
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spelling pubmed-84459442021-09-20 Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma Scheibenpflug, Raphael Obermüller, Markus Reznicek, Gottfried Neuper, Ortrun Lamm, Wolfgang W. Raderer, Markus Lagler, Heimo Sci Rep Article In view of the antineoplastic effects of the macrolide clarithromycin in mucosa associated lymphatic tissue (MALT)-lymphoma, we performed a pilot study assessing levels of azithromycin in plasma, peripheral blood mononuclear cells (PBMC) and polymorphonuclear leukocytes (PMN) of MALT-lymphoma patients to determine the pharmacokinetics and potential influences of respective concentrations on the therapeutic outcome. In total 16 patients with MALT-lymphoma received 1.5 g of oral azithromycin once-weekly over 6 months. Blood was sampled directly prior to the following dose every 4 weeks during treatment. Drug levels were analysed by high performance liquid chromatography in plasma and intracellularly in PBMC and PMN. They were correlated with patients’ age, weight and body-mass-index and compared between patients responsive or unresponsive to treatment. Mean azithromycin plasma levels of all patients were 58.97 ± 30.48 ng/ml, remaining stable throughout the treatment period. Correlation analysis of plasma azithromycin showed no significance. Intracellular PBMC concentrations were 6648 ± 8479 ng/ml, without any significant difference between responders and non-responders. Mean PMN levels were 39,274 ± 25,659 ng/ml and significantly higher in patients unresponsive to treatment (t = 2.858, p = 0.017). Our drug regime led to continuously high plasma and exceedingly high intracellular concentrations of azithromycin in PBMC and PMN. Age, weight or body-mass-index had no significant influence on plasma levels and thence should not be considered in dosage finding. High AZM levels in PBMC did not lead to a better treatment response, whereas enrichment in PMN suggested a poorer outcome. The threshold for immunomodulatory effects on lymphoma cells might not have been reached. Additionally, the finding of stable plasma and intracellular concentrations over months with high-dose azithromycin administered in intervals might also be important for the further design of azithromycin-based trials against MALT-lymphoma. Trial registration: EudraCT 2016-001521-13, 14/06/2016. Nature Publishing Group UK 2021-09-16 /pmc/articles/PMC8445944/ /pubmed/34531427 http://dx.doi.org/10.1038/s41598-021-97836-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Scheibenpflug, Raphael
Obermüller, Markus
Reznicek, Gottfried
Neuper, Ortrun
Lamm, Wolfgang W.
Raderer, Markus
Lagler, Heimo
Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title_full Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title_fullStr Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title_full_unstemmed Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title_short Azithromycin concentrations during long-term regimen, a pilot study in patients with MALT lymphoma
title_sort azithromycin concentrations during long-term regimen, a pilot study in patients with malt lymphoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445944/
https://www.ncbi.nlm.nih.gov/pubmed/34531427
http://dx.doi.org/10.1038/s41598-021-97836-w
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