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Cyp2d6*10 polymorphisms on tamoxifen metabolism in breast cancer patients
- In: Posters G - Pharmacokinetics (PK), Pharmacodynamics (PD) and Systems Pharmacology
- At: PSWC, Melbourne (Australia) (2014)
- Type: Poster
- Poster code: PG-037
- By: PAO, Li-Heng (Chang Gung University of Science and Technology, Research Center for Industry of Human Ecology, Taoyuan, China Taiwan)
- Co-author(s): Ho, Ya-Ting (School of Pharmacy, National Defense Medical Center, Taipei, China Taiwan)
Lo, Chia-Yi (Department of Pharmacy Practice, Tri-Service General Hospital, Taipei, China Taiwan)
Dai, Ming-Shen (Department of Hematology and Oncology, Tri-Service General Hospital, Taipei, China Taiwan)
Shih, Jui-Hu (Department of Pharmacy Practice, Tri-Service General Hospital, Taipei, China Taiwan) - Abstract:
Background: Tamoxifen has been the gold standard for reducing the risk of recurrence and mortality in adjuvant endocrine therapy. The active metabolites of tamoxifen, 4-hydroxytamoxifen and 4-hydroxy-N-desmethyltamoxifen (endoxifen), have been considered to have 100-fold greater affinity for estrogen receptors than the parent drug. Several study..
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Last update 28 September 2023