| Literature DB >> 32578187 |
Anna Mueller-Schoell1,2, Lena Klopp-Schulze1, Werner Schroth3,4, Thomas Mürdter3,4, Robin Michelet1, Hiltrud Brauch3,4,5, Wilhelm Huisinga6, Markus Joerger7, Patrick Neven8, Stijn L W Koolen9, Ron H J Mathijssen9, Ellen Copson10,11, Diana Eccles10,11, Sylvia Chen12, Balram Chowbay12,13,14, Arafat Tfayli15, Nathalie K Zgheib16, Matthias Schwab3,5,17, Charlotte Kloft1.
Abstract
Endoxifen is one of the most important metabolites of the prodrug tamoxifen. High interindividual variability in endoxifen steady-state concentrations (CSS,min ENDX ) is observed under tamoxifen standard dosing and patients with breast cancer who do not reach endoxifen concentrations above a proposed therapeutic threshold of 5.97 ng/mL may be at a 26% higher recurrence risk compared with patients with endoxifen concentrations exceeding this value. In this investigation, 10 clinical tamoxifen studies were pooled (1,388 patients) to investigate influential factors on CSS,min ENDX using nonlinear mixed-effects modeling. Age and body weight were found to significantly impact CSS,min ENDX in addition to CYP2D6 phenotype. Compared with postmenopausal patients, premenopausal patients had a 30% higher risk for subtarget CSS,min ENDX at tamoxifen 20 mg per day. In treatment simulations for distinct patient subpopulations, young overweight patients had a 3.1-13.8-fold higher risk for subtarget CSS,min ENDX compared with elderly low-weight patients. Considering ever-rising obesity rates and the clinical importance of tamoxifen for premenopausal patients, this subpopulation may benefit most from individualized tamoxifen dosing.Entities:
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Year: 2020 PMID: 32578187 DOI: 10.1002/cpt.1960
Source DB: PubMed Journal: Clin Pharmacol Ther ISSN: 0009-9236 Impact factor: 6.875