Factors Affecting Tamoxifen Metabolism in Patients With Breast Cancer: Preliminary Results of the French PHACS Study. Issue 3 (10th April 2019)
- Record Type:
- Journal Article
- Title:
- Factors Affecting Tamoxifen Metabolism in Patients With Breast Cancer: Preliminary Results of the French PHACS Study. Issue 3 (10th April 2019)
- Main Title:
- Factors Affecting Tamoxifen Metabolism in Patients With Breast Cancer: Preliminary Results of the French PHACS Study
- Authors:
- Puszkiel, Alicja
Arellano, Cécile
Vachoux, Christelle
Evrard, Alexandre
Le Morvan, Valérie
Boyer, Jean‐Christophe
Robert, Jacques
Delmas, Caroline
Dalenc, Florence
Debled, Marc
Venat‐Bouvet, Laurence
Jacot, William
Suc, Etienne
Sillet‐Bach, Isabelle
Filleron, Thomas
Roché, Henri
Chatelut, Etienne
White‐Koning, Melanie
Thomas, Fabienne - Abstract:
- Abstract : In addition to the effect of cytochrome P450 ( CYP ) 2D6 genetic polymorphisms, the metabolism of tamoxifen may be impacted by other factors with possible consequences on therapeutic outcome (efficacy and toxicity). This analysis focused on the pharmacokinetic (PK)‐pharmacogenetic evaluation of tamoxifen in 730 patients with adjuvant breast cancer included in a prospective multicenter study. Plasma concentrations of tamoxifen and six major metabolites, the genotype for 63 single‐nucleotide polymorphisms, and comedications were obtained 6 months after treatment initiation. Plasma concentrations of endoxifen were significantly associated with CYP2D6 diplotype ( P < 0.0001), CYP3A4*22 genotype ( P = 0.0003), and concomitant intake of potent CYP2D6 inhibitors ( P < 0.001). Comparison of endoxifen levels showed that the CYP2D6 phenotype classification could be improved by grouping intermediate metabolizer (IM)/IM and IM/poor metabolizer diplotype into IM phenotype for future use in tamoxifen therapy optimization. Finally, the multivariable regression analysis showed that formation of tamoxifen metabolites was independently impacted by CYP2D6 diplotype and CYP3A4*22, CYP2C19*2, and CYP2B6*6 genetic polymorphisms.
- Is Part Of:
- Clinical pharmacology & therapeutics. Volume 106:Issue 3(2019)
- Journal:
- Clinical pharmacology & therapeutics
- Issue:
- Volume 106:Issue 3(2019)
- Issue Display:
- Volume 106, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 106
- Issue:
- 3
- Issue Sort Value:
- 2019-0106-0003-0000
- Page Start:
- 585
- Page End:
- 595
- Publication Date:
- 2019-04-10
- Subjects:
- Pharmacology -- Periodicals
Therapeutics -- Periodicals
615.5 - Journal URLs:
- http://www.nature.com/clpt/index.html ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1532-6535 ↗
http://www.nature.com/ ↗
http://firstsearch.oclc.org ↗
http://www.mosby.com/cpt ↗
http://www.sciencedirect.com/science/journal/00099236 ↗
http://www2.us.elsevierhealth.com/scripts/om.dll/serve?action=searchDB&searchdbfor=home&id=cp ↗ - DOI:
- 10.1002/cpt.1404 ↗
- Languages:
- English
- ISSNs:
- 0009-9236
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.330000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20679.xml