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Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl

BACKGROUND AND OBJECTIVES: The cutaneous fentanyl patch is widely used to treat continuous pain in patients with cancer. Its use is hampered by a high inter- and intrapatient pharmacokinetic variability. Factors that influence this pharmacokinetic variability are largely unclear. The aim of these st...

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Autores principales: Kuip, Evelien J.M., Oldenmenger, Wendy H., Visser-Thijs, Martine F., de Bruijn, Peter, Oomen-de Hoop, Esther, Mathijssen, Ron H.J., Van der Rijt, Carin C.D., Koolen, Stijn W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915071/
https://www.ncbi.nlm.nih.gov/pubmed/29719604
http://dx.doi.org/10.18632/oncotarget.24812
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author Kuip, Evelien J.M.
Oldenmenger, Wendy H.
Visser-Thijs, Martine F.
de Bruijn, Peter
Oomen-de Hoop, Esther
Mathijssen, Ron H.J.
Van der Rijt, Carin C.D.
Koolen, Stijn W.
author_facet Kuip, Evelien J.M.
Oldenmenger, Wendy H.
Visser-Thijs, Martine F.
de Bruijn, Peter
Oomen-de Hoop, Esther
Mathijssen, Ron H.J.
Van der Rijt, Carin C.D.
Koolen, Stijn W.
author_sort Kuip, Evelien J.M.
collection PubMed
description BACKGROUND AND OBJECTIVES: The cutaneous fentanyl patch is widely used to treat continuous pain in patients with cancer. Its use is hampered by a high inter- and intrapatient pharmacokinetic variability. Factors that influence this pharmacokinetic variability are largely unclear. The aim of these studies was to test if common patient variables, i) the use of the moderate CYP3A4 inhibitor aprepitant and ii) the localization of the fentanyl patch (upper arm versus thorax) influence systemic exposure to fentanyl in patients with cancer using a transdermal fentanyl patch. RESULTS: The AUC(0–6 h) of fentanyl was 7.1% (95% CI: −28% to +19%) lower if patients concurrently used aprepitant, compared to the period when patients used fentanyl only. The AUC(0–4 h) of fentanyl was 7.4% (95% CI: −22% to +49%) higher when the cutaneous fentanyl patch was applied to the upper arm compared to application at the thorax. CONCLUSIONS: Neither the concurrent use of aprepitant, nor the localization of the fentanyl patch showed a statistically significant influence on fentanyl pharmacokinetics. METHODS: We performed two prospective cross-over pharmacokinetic intervention studies. Both studies had two eight-day study periods. At day 8 of each study period blood samples were collected for pharmacokinetic analysis. In each study 14 evaluable patients were included.
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spelling pubmed-59150712018-05-01 Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl Kuip, Evelien J.M. Oldenmenger, Wendy H. Visser-Thijs, Martine F. de Bruijn, Peter Oomen-de Hoop, Esther Mathijssen, Ron H.J. Van der Rijt, Carin C.D. Koolen, Stijn W. Oncotarget Research Paper BACKGROUND AND OBJECTIVES: The cutaneous fentanyl patch is widely used to treat continuous pain in patients with cancer. Its use is hampered by a high inter- and intrapatient pharmacokinetic variability. Factors that influence this pharmacokinetic variability are largely unclear. The aim of these studies was to test if common patient variables, i) the use of the moderate CYP3A4 inhibitor aprepitant and ii) the localization of the fentanyl patch (upper arm versus thorax) influence systemic exposure to fentanyl in patients with cancer using a transdermal fentanyl patch. RESULTS: The AUC(0–6 h) of fentanyl was 7.1% (95% CI: −28% to +19%) lower if patients concurrently used aprepitant, compared to the period when patients used fentanyl only. The AUC(0–4 h) of fentanyl was 7.4% (95% CI: −22% to +49%) higher when the cutaneous fentanyl patch was applied to the upper arm compared to application at the thorax. CONCLUSIONS: Neither the concurrent use of aprepitant, nor the localization of the fentanyl patch showed a statistically significant influence on fentanyl pharmacokinetics. METHODS: We performed two prospective cross-over pharmacokinetic intervention studies. Both studies had two eight-day study periods. At day 8 of each study period blood samples were collected for pharmacokinetic analysis. In each study 14 evaluable patients were included. Impact Journals LLC 2018-04-06 /pmc/articles/PMC5915071/ /pubmed/29719604 http://dx.doi.org/10.18632/oncotarget.24812 Text en Copyright: © 2018 Kuip et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kuip, Evelien J.M.
Oldenmenger, Wendy H.
Visser-Thijs, Martine F.
de Bruijn, Peter
Oomen-de Hoop, Esther
Mathijssen, Ron H.J.
Van der Rijt, Carin C.D.
Koolen, Stijn W.
Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title_full Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title_fullStr Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title_full_unstemmed Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title_short Influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
title_sort influence of aprepitant and localization of the patch on fentanyl exposure in patients with cancer using transdermal fentanyl
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915071/
https://www.ncbi.nlm.nih.gov/pubmed/29719604
http://dx.doi.org/10.18632/oncotarget.24812
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