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Marginal increase of sunitinib exposure by grapefruit juice

PURPOSE: The drug label of sunitinib includes a warning for concomitant use of grapefruit juice (GJ) but clinical evidence for this drug interaction is lacking. The aim of this study is to determine the effect of GJ, a potent intestinal cytochrome P450 (CYP) 3A4 inhibitor, on steady-state sunitinib...

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Autores principales: van Erp, Nielka P., Baker, Sharyn D., Zandvliet, Anthe S., Ploeger, Bart A., den Hollander, Margaret, Chen, Zhaoyuan, den Hartigh, Jan, König-Quartel, Jacqueline M. C., Guchelaar, Henk-Jan, Gelderblom, Hans
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043256/
https://www.ncbi.nlm.nih.gov/pubmed/20512335
http://dx.doi.org/10.1007/s00280-010-1367-0
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author van Erp, Nielka P.
Baker, Sharyn D.
Zandvliet, Anthe S.
Ploeger, Bart A.
den Hollander, Margaret
Chen, Zhaoyuan
den Hartigh, Jan
König-Quartel, Jacqueline M. C.
Guchelaar, Henk-Jan
Gelderblom, Hans
author_facet van Erp, Nielka P.
Baker, Sharyn D.
Zandvliet, Anthe S.
Ploeger, Bart A.
den Hollander, Margaret
Chen, Zhaoyuan
den Hartigh, Jan
König-Quartel, Jacqueline M. C.
Guchelaar, Henk-Jan
Gelderblom, Hans
author_sort van Erp, Nielka P.
collection PubMed
description PURPOSE: The drug label of sunitinib includes a warning for concomitant use of grapefruit juice (GJ) but clinical evidence for this drug interaction is lacking. The aim of this study is to determine the effect of GJ, a potent intestinal cytochrome P450 (CYP) 3A4 inhibitor, on steady-state sunitinib pharmacokinetics (PK). METHODS: Sunitinib PK was evaluated in eight cancer patients receiving sunitinib monotherapy in a “4 weeks on—2 weeks off” dose regimen. Serial blood samples for PK analysis of sunitinib were collected on two separate days. On both PK days, patients received a single oral dose of 7.5-mg midazolam as a phenotypic probe for assessment of intestinal CYP3A4 activity. The first PK day was at steady-state sunitinib PK (between days 14–20), the second PK day was on day 28. On days 25, 26 and 27, 200-mL GJ was consumed 3 times a day. The effect of GJ on sunitinib exposure was assessed by comparing sunitinib PK with and without GJ. RESULTS: Concomitant use of GJ and sunitinib resulted in an 11% increase of the relative bioavailability of sunitinib (P < 0.05). The effect of GJ on CYP3A4 activity was confirmed by an increase of ~50% of mean midazolam exposure (AUC(0–24 h)) from 122.1 to 182.0 ng h/mL (P = 0.034). CONCLUSION: GJ consumption results in a marginal increase in sunitinib exposure which is not considered clinically relevant. There is no clinical evidence underscoring the warning in the sunitinib drug label regarding concomitant use of GJ.
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spelling pubmed-30432562011-04-04 Marginal increase of sunitinib exposure by grapefruit juice van Erp, Nielka P. Baker, Sharyn D. Zandvliet, Anthe S. Ploeger, Bart A. den Hollander, Margaret Chen, Zhaoyuan den Hartigh, Jan König-Quartel, Jacqueline M. C. Guchelaar, Henk-Jan Gelderblom, Hans Cancer Chemother Pharmacol Original Article PURPOSE: The drug label of sunitinib includes a warning for concomitant use of grapefruit juice (GJ) but clinical evidence for this drug interaction is lacking. The aim of this study is to determine the effect of GJ, a potent intestinal cytochrome P450 (CYP) 3A4 inhibitor, on steady-state sunitinib pharmacokinetics (PK). METHODS: Sunitinib PK was evaluated in eight cancer patients receiving sunitinib monotherapy in a “4 weeks on—2 weeks off” dose regimen. Serial blood samples for PK analysis of sunitinib were collected on two separate days. On both PK days, patients received a single oral dose of 7.5-mg midazolam as a phenotypic probe for assessment of intestinal CYP3A4 activity. The first PK day was at steady-state sunitinib PK (between days 14–20), the second PK day was on day 28. On days 25, 26 and 27, 200-mL GJ was consumed 3 times a day. The effect of GJ on sunitinib exposure was assessed by comparing sunitinib PK with and without GJ. RESULTS: Concomitant use of GJ and sunitinib resulted in an 11% increase of the relative bioavailability of sunitinib (P < 0.05). The effect of GJ on CYP3A4 activity was confirmed by an increase of ~50% of mean midazolam exposure (AUC(0–24 h)) from 122.1 to 182.0 ng h/mL (P = 0.034). CONCLUSION: GJ consumption results in a marginal increase in sunitinib exposure which is not considered clinically relevant. There is no clinical evidence underscoring the warning in the sunitinib drug label regarding concomitant use of GJ. Springer-Verlag 2010-05-29 2011 /pmc/articles/PMC3043256/ /pubmed/20512335 http://dx.doi.org/10.1007/s00280-010-1367-0 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
van Erp, Nielka P.
Baker, Sharyn D.
Zandvliet, Anthe S.
Ploeger, Bart A.
den Hollander, Margaret
Chen, Zhaoyuan
den Hartigh, Jan
König-Quartel, Jacqueline M. C.
Guchelaar, Henk-Jan
Gelderblom, Hans
Marginal increase of sunitinib exposure by grapefruit juice
title Marginal increase of sunitinib exposure by grapefruit juice
title_full Marginal increase of sunitinib exposure by grapefruit juice
title_fullStr Marginal increase of sunitinib exposure by grapefruit juice
title_full_unstemmed Marginal increase of sunitinib exposure by grapefruit juice
title_short Marginal increase of sunitinib exposure by grapefruit juice
title_sort marginal increase of sunitinib exposure by grapefruit juice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3043256/
https://www.ncbi.nlm.nih.gov/pubmed/20512335
http://dx.doi.org/10.1007/s00280-010-1367-0
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