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Published in: Clinical Pharmacokinetics 2/2016

Open Access 01-02-2016 | Original Research Article

Augmentation of Endoxifen Exposure in Tamoxifen-Treated Women Following SSRI Switch

Authors: Lisette Binkhorst, Marjolein Bannink, Peter de Bruijn, Jan Ruit, Helga Droogendijk, Robbert J. van Alphen, Tilly D. den Boer, Mei Ho Lam, Agnes Jager, Teun van Gelder, Ron H. J. Mathijssen

Published in: Clinical Pharmacokinetics | Issue 2/2016

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Abstract

Background and Objective

The anti-oestrogen tamoxifen requires metabolic activation to endoxifen by cytochrome P450 (CYP) enzymes, predominantly CYP2D6. Potent CYP2D6-inhibiting antidepressants can seriously disrupt tamoxifen metabolism, probably influencing the efficacy of tamoxifen. For this reason, paroxetine and fluoxetine are recommended not to be used with tamoxifen in breast cancer patients. We investigated the effects of switching potent CYP2D6-inhibiting antidepressants to weak CYP2D6-inhibiting antidepressants on the plasma pharmacokinetics of tamoxifen.

Methods

Ten breast cancer patients who were treated with tamoxifen in combination with a potent CYP2D6-inhibiting antidepressant (paroxetine or fluoxetine) for at least 4 weeks were enrolled. Under close supervision by a psychiatrist, patients were switched to treatment with escitalopram or venlafaxine (weak CYP2D6-inhibiting antidepressants). Before and after the switch, pharmacokinetic blood sampling was performed over 24 h. Pharmacokinetic parameters were estimated using noncompartmental analysis. Adverse effects were recorded during the study.

Results

Endoxifen exposure was ~3-fold higher during escitalopram co-administration than during paroxetine or fluoxetine co-administration (median 387 nM·h [range 159–637 nM·h] versus 99.2 nM·h [range 70.0–210 nM·h]; P = 0.012; Wilcoxon signed-rank test). The ratio of endoxifen to N-desmethyltamoxifen and the ratio of 4-hydroxytamoxifen to tamoxifen increased by 3.3- and ~1.5-fold, reflecting increased CYP2D6 activity. Antidepressant switching did not result in psychiatric problems or antidepressant-related adverse effects.

Conclusion

In this study, switching to the weak CYP2D6 inhibitor escitalopram was safe and feasible and resulted in clinically relevant rises in endoxifen concentrations. We therefore advise switching paroxetine and fluoxetine to escitalopram in patients using tamoxifen. However, switching should always be weighed in individual patients.
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Metadata
Title
Augmentation of Endoxifen Exposure in Tamoxifen-Treated Women Following SSRI Switch
Authors
Lisette Binkhorst
Marjolein Bannink
Peter de Bruijn
Jan Ruit
Helga Droogendijk
Robbert J. van Alphen
Tilly D. den Boer
Mei Ho Lam
Agnes Jager
Teun van Gelder
Ron H. J. Mathijssen
Publication date
01-02-2016
Publisher
Springer International Publishing
Published in
Clinical Pharmacokinetics / Issue 2/2016
Print ISSN: 0312-5963
Electronic ISSN: 1179-1926
DOI
https://doi.org/10.1007/s40262-015-0315-x

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