Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
about
Endoxifen's molecular mechanisms of action are concentration dependent and different than that of other anti-estrogensIdentification of drug metabolites in human plasma or serum integrating metabolite prediction, LC-HRMS and untargeted data processing.Concomitant use of tamoxifen and endoxifen in postmenopausal early breast cancer: prediction of plasma levels by physiologically-based pharmacokinetic modeling.Tamoxifen and CYP2D6: a contradiction of data.Use of CYP2D6 genotyping in practice: tamoxifen dose adjustment.Effects of CYP induction by rifampicin on tamoxifen exposure.Pharmacogenomics of drug-metabolizing enzymes: a recent update on clinical implications and endogenous effects.Individualization of tamoxifen treatment for breast carcinoma.Population pharmacokinetic modelling to assess the impact of CYP2D6 and CYP3A metabolic phenotypes on the pharmacokinetics of tamoxifen and endoxifenPharmacological relevance of endoxifen in a laboratory simulation of breast cancer in postmenopausal patients.Unjustified prescribing of CYP2D6 inhibiting SSRIs in women treated with tamoxifen.Tamoxifen metabolism predicts drug concentrations and outcome in premenopausal patients with early breast cancer.Hot flashes are not predictive for serum concentrations of tamoxifen and its metabolites.Evaluation of tamoxifen and metabolites by LC-MS/MS and HPLC methods.Pharmacokinetics of endoxifen and tamoxifen in female mice: implications for comparative in vivo activity studies.Evaluation of CYP2D6 enzyme activity using a 13C-dextromethorphan breath test in women receiving adjuvant tamoxifen.Drug metabolizing enzyme activities versus genetic variances for drug of clinical pharmacogenomic relevance.Evaluation of CYP2D6 and efficacy of tamoxifen and raloxifene in women treated for breast cancer chemoprevention: results from the NSABP P1 and P2 clinical trials.Limited predictive value of achieving beneficial plasma (Z)-endoxifen threshold level by CYP2D6 genotyping in tamoxifen-treated Polish women with breast cancer.Circadian variation in tamoxifen pharmacokinetics in mice and breast cancer patients.CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the breast international group 1-98 trial.Effects of Pharmacogenetics on the Pharmacokinetics and Pharmacodynamics of Tamoxifen.Clinical and biomarker predictors of side effects from tamoxifenBoronic prodrug of endoxifen as an effective hormone therapy for breast cancer.Physiologically Based Pharmacokinetic Modeling of Tamoxifen and its Metabolites in Women of Different CYP2D6 Phenotypes Provides New Insight into the Tamoxifen Mass Balance.Importance of highly selective LC-MS/MS analysis for the accurate quantification of tamoxifen and its metabolites: focus on endoxifen and 4-hydroxytamoxifenProfound reduction in tamoxifen active metabolite endoxifen in a breast cancer patient treated with rifampin prior to initiation of an anti-TNFα biologic for ulcerative colitis: a case report.Loss of heterozygosity at the CYP2D6 locus in breast cancer: implications for germline pharmacogenetic studies.Tissue distribution of 4-hydroxy-N-desmethyltamoxifen and tamoxifen-N-oxide.CYP2D6 genotype- and endoxifen-guided tamoxifen dose escalation increases endoxifen serum concentrations without increasing side effects.National Prociency Testing Result of CYP2D6*10 Genotyping for Adjuvant Tamoxifen Therapy in China.In vivo assessment of the metabolic activity of CYP2D6 diplotypes and alleles.Role of cytochrome P450 genotype in the steps toward personalized drug therapy.Leveraging epidemiology and clinical studies of cancer outcomes: recommendations and opportunities for translational researchCYP2D6 metabolism and patient outcome in the Austrian Breast and Colorectal Cancer Study Group trial (ABCSG) 8.Functional polymorphisms in xenobiotic metabolizing enzymes and their impact on the therapy of breast cancer.Augmentation of Endoxifen Exposure in Tamoxifen-Treated Women Following SSRI SwitchAnnexin-A1 and caldesmon are associated with resistance to tamoxifen in estrogen receptor positive recurrent breast cancer.Cancer pharmacogenomicsIndividualized Tamoxifen Dose Escalation: Confirmation of Feasibility, Question of Utility.
P2860
Q28485336-4477040D-2146-4C8A-8BAA-EDF65A6A9DFCQ30662550-23CA1842-1E54-4FED-BF60-13FD5E51FCE4Q33756964-0C66760C-1E3F-4F5F-AF74-85EC73454F8FQ34244463-9B221427-7846-40E7-AC93-81D215E1B656Q34269380-CF0D3281-17F2-43A4-8DBE-326B8CD4813EQ34278391-D2E797ED-603A-496C-927D-09326CE79D77Q34307589-AD94DFB6-DBA8-4237-9658-4C66926A8885Q34387066-83CE35C1-9CE7-4B04-A3DC-CF49AC680548Q34571065-700AA6ED-1180-4A85-9B76-45845B139B05Q34736986-F0343163-3E12-4255-B176-9987A22C2A87Q34768999-BE514366-5118-48FC-90B3-869F89CF85FFQ35020403-492FFEC9-E4B0-496D-A0F5-9749564C8B11Q35076890-27764355-D96D-4BB6-AD99-C0ACBD6E9024Q35111746-7AADE1B9-79AD-4A12-AAC6-BF991AF39403Q35129546-7C544585-9417-467B-A95F-8B1E349288C1Q35168556-E7DAFAEB-0D0D-4C38-8E34-A7A67AF06718Q35206306-C4494C40-C481-4EA4-A283-AABA1C9477EBQ35510803-2658D64D-2900-4DAB-B236-32D97F3BD1F1Q35732619-A7E8166D-2919-44B6-985E-940239AF79B8Q35747766-D6C70883-C444-411C-8F91-30FA4D83BD5CQ35842986-6F7EF74A-9684-425D-8422-AAF6B388B32BQ35884159-DD856780-CD5B-4C95-A8EE-2352BE515A51Q35911174-E43CB394-1B5F-4079-A680-8085CB5E2EE6Q35915042-1FBE59EB-47DB-4587-ABCE-52B1DE1D63B2Q35975826-CC21CB64-0EB6-498A-844B-AF34BC0CD15DQ35996187-09653138-A4B4-49C6-A0C3-D978583D9E31Q36015010-B1DDF144-2AA7-43C6-A98B-8E03651789B7Q36047387-FF5BA973-3988-45F3-BDCB-D2719CAD64CBQ36107130-2A5C1763-3C23-434F-BCA0-AB561D8E19CFQ36109257-99B9992F-5E01-4D5E-9BB0-D6F4E8549D32Q36125233-77D998E2-B1D8-4AD6-A029-67AB52331641Q36243663-0230A517-E2A5-438A-BBC2-69B71428991DQ36441521-8E6D6EB0-D0E9-4243-B1DA-66F3A19246BDQ36535678-C604A733-2F17-4249-BF57-A1FC16BBE5D6Q36545056-C45BC0DE-0EBD-4962-A054-B77CE34F2C86Q36550926-C9DD291D-F431-430E-A90E-FB27352B0601Q36586900-67DE646A-6658-4A1F-84BD-9885802066CFQ36772047-028C7ABD-00EB-42EE-B8CF-E6274E4C30AAQ36822291-A823E6B6-8A17-40A9-9576-2CF95775EB62Q37059751-635D4CF6-DFA2-48CA-9921-33DA5C5DF383
P2860
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@ast
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@en
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@nl
type
label
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@ast
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@en
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@nl
prefLabel
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@ast
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@en
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes.
@nl
P2093
P2860
P356
P1476
Tamoxifen metabolite concentrations, CYP2D6 genotype, and breast cancer outcomes
@en
P2093
B A Parker
D M Nikoloff
H J Lawrence
J P Pierce
L Madlensky
L Natarajan
M R Fontecha
P2860
P304
P356
10.1038/CLPT.2011.32
P407
P577
2011-03-23T00:00:00Z