Literature DB >> 25997856

Tailored Tamoxifen Treatment for Breast Cancer Patients: A Perspective.

Nynke G L Jager1, Sabine C Linn2, Jan H M Schellens3, Jos H Beijnen4.   

Abstract

Tamoxifen, an endocrine agent, is widely used in the treatment of estrogen receptor-positive breast cancer. It has greatly reduced disease recurrence and mortality rates of breast cancer patients, however, not all patients benefit from tamoxifen treatment because in approximately 25% to 30% of the patients the disease recurs. Many researchers have sought to find factors associated with endocrine treatment outcome in the past years, however, this quest has not been finished. In this article, we focus on a factor that might influence outcome of tamoxifen treatment: interpatient variability in tamoxifen pharmacokinetics. In recent years it has become clear that tamoxifen undergoes extensive metabolism and that some of the formed metabolites are much more pharmacologically active than tamoxifen itself. Despite the wide interpatient variability in tamoxifen pharmacokinetics and pharmacodynamics, all patients receive a standard dose of 20 mg tamoxifen per day. Different approaches can be pursued to individualize tamoxifen dosing: genotyping, phenotyping, and therapeutic drug monitoring. Therapeutic drug monitoring seems to be the most direct and promising approach, however, further clinical research is warranted to establish the added value of individual dosing in tamoxifen treatment optimization.
Copyright © 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Endoxifen; Estrogen receptor-positive breast cancer; Metabolite levels; Therapeutic Drug Monitoring; Treatment individualization

Mesh:

Substances:

Year:  2015        PMID: 25997856     DOI: 10.1016/j.clbc.2015.04.005

Source DB:  PubMed          Journal:  Clin Breast Cancer        ISSN: 1526-8209            Impact factor:   3.225


  8 in total

1.  An Antiestrogenic Activity Score for tamoxifen and its metabolites is associated with breast cancer outcome.

Authors:  A H M de Vries Schultink; X Alexi; E van Werkhoven; L Madlensky; L Natarajan; S W Flatt; W Zwart; S C Linn; B A Parker; A H B Wu; J P Pierce; A D R Huitema; J H Beijnen
Journal:  Breast Cancer Res Treat       Date:  2016-12-22       Impact factor: 4.872

2.  Baicalein, unlike 4-hydroxytamoxifen but similar to G15, suppresses 17β-estradiol-induced cell invasion, and matrix metalloproteinase-9 expression and activation in MCF-7 human breast cancer cells.

Authors:  Yan Chen; Duan-Yang Hong; Jing Wang; Jun Ling-Hu; Yan-Yan Zhang; Di Pan; Yi-Ni Xu; Ling Tao; Hong Luo; Xiang-Chun Shen
Journal:  Oncol Lett       Date:  2017-06-02       Impact factor: 2.967

Review 3.  Systemic treatments for metastatic cutaneous melanoma.

Authors:  Sandro Pasquali; Andreas V Hadjinicolaou; Vanna Chiarion Sileni; Carlo Riccardo Rossi; Simone Mocellin
Journal:  Cochrane Database Syst Rev       Date:  2018-02-06

4.  Serum concentrations of active tamoxifen metabolites predict long-term survival in adjuvantly treated breast cancer patients.

Authors:  Thomas Helland; Nina Henne; Ersilia Bifulco; Bjørn Naume; Elin Borgen; Vessela N Kristensen; Jan T Kvaløy; Timothy L Lash; Grethe I G Alnæs; Ron H van Schaik; Emiel A M Janssen; Steinar Hustad; Ernst A Lien; Gunnar Mellgren; Håvard Søiland
Journal:  Breast Cancer Res       Date:  2017-11-28       Impact factor: 6.466

5.  Paeoniflorin Sensitizes Breast Cancer Cells to Tamoxifen by Downregulating microRNA-15b via the FOXO1/CCND1/β-Catenin Axis.

Authors:  Yanhong Wang; Qian Wang; Xibei Li; Gongwen Luo; Mou Shen; Jia Shi; Xueliang Wang; Lu Tang
Journal:  Drug Des Devel Ther       Date:  2021-01-22       Impact factor: 4.162

6.  Analysis of tamoxifen and its metabolites in dried blood spot and volumetric absorptive microsampling: comparison and clinical application.

Authors:  Baitha Palanggatan Maggadani; Yahdiana Harahap; Samuel J Haryono; Christoffel William Putra Untu
Journal:  Heliyon       Date:  2021-06-10

Review 7.  Tamoxifen Resistance: Emerging Molecular Targets.

Authors:  Milena Rondón-Lagos; Victoria E Villegas; Nelson Rangel; Magda Carolina Sánchez; Peter G Zaphiropoulos
Journal:  Int J Mol Sci       Date:  2016-08-19       Impact factor: 5.923

8.  Upregulation of SOX11 enhances tamoxifen resistance and promotes epithelial-to-mesenchymal transition via slug in MCF-7 breast cancer cells.

Authors:  Yingsheng Xiao; Qin Xie; Qingsong Qin; Yuanke Liang; Haoyu Lin
Journal:  J Cell Physiol       Date:  2020-02-11       Impact factor: 6.384

  8 in total

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