Literature DB >> 15039600

Association of tamoxifen (TAM) and TAM metabolite concentrations with self-reported side effects of TAM in women with breast cancer.

Lisa Gallicchio1, Gwyn Lord, Katherine Tkaczuk, Malcolm Danton, Lynn M Lewis, Chang K Lim, Jodi A Flaws.   

Abstract

The positive effects of tamoxifen (TAM) on breast cancer recurrence and survival as well as on overall mortality have led to its use as the predominant adjuvant therapy among women with breast cancer. However, the association of TAM intake with undesirable side effects has been reported in numerous studies. This analysis was carried out to assess whether the concentrations of TAM or TAM metabolites, N -desmethyltamoxifen ( N -DMT) and 4-hydroxytamoxifen (4-OHT), were associated with self-reported side effects of TAM. Participants were 99 breast cancer patients who had been taking TAM for at least 30 days. Each participant completed a questionnaire that was used to ascertain whether she experienced certain specific symptoms while taking TAM. In addition, each woman provided a blood sample that was used to measure plasma concentrations of TAM, N -DMT, and 4-OHT by high performance liquid chromatography. Results of the analysis showed that women who experienced at least one TAM-related side effect had significantly higher levels of TAM than women not experiencing any TAM-related side effects. Furthermore, women who reported experiencing visual problems had significantly higher levels of both TAM and N -DMT compared to those women who reported experiencing no visual problems. The levels of 4-OHT were negatively associated with the occurrence of vaginal discharge. The results of this study suggest that the self-reported occurrence of certain symptoms during TAM treatment is related to TAM metabolism. Future studies should assess subgroups of women with specific TAM and TAM metabolite profiles to determine whether alternate, equally effective therapies would decrease their risk of experiencing certain undesirable side effects.

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Year:  2004        PMID: 15039600     DOI: 10.1023/B:BREA.0000021050.92539.b0

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  13 in total

Review 1.  A review on the role of L-carnitine in the management of tamoxifen side effects in treated women with breast cancer.

Authors:  Nahla E El-Ashmawy; Rania M Khalil
Journal:  Tumour Biol       Date:  2013-12-12

2.  Phenotype anchoring in zebrafish reveals a potential role for matrix metalloproteinases (MMPs) in tamoxifen's effects on skin epithelium.

Authors:  Sean M Bugel; Leah C Wehmas; Jane K La Du; Robert L Tanguay
Journal:  Toxicol Appl Pharmacol       Date:  2016-02-18       Impact factor: 4.219

3.  Chemoprevention of Breast Cancer by Transdermal Delivery of α-Santalol through Breast Skin and Mammary Papilla (Nipple).

Authors:  Kaushalkumar Dave; Fahd M Alsharif; Saiful Islam; Chandradhar Dwivedi; Omathanu Perumal
Journal:  Pharm Res       Date:  2017-06-06       Impact factor: 4.200

4.  Associations between tamoxifen, estrogens, and FSH serum levels during steady state tamoxifen treatment of postmenopausal women with breast cancer.

Authors:  Jennifer Gjerde; Jürgen Geisler; Steinar Lundgren; Dagfinn Ekse; Jan Erik Varhaug; Gunnar Mellgren; Vidar M Steen; Ernst A Lien
Journal:  BMC Cancer       Date:  2010-06-21       Impact factor: 4.430

Review 5.  Breast cancer medications and vision: effects of treatments for early-stage disease.

Authors:  Alvin Eisner; Shiuh-Wen Luoh
Journal:  Curr Eye Res       Date:  2011-08-05       Impact factor: 2.424

6.  Differential effects of tamoxifen and anastrozole on optic cup size in breast cancer survivors.

Authors:  Alvin Eisner; Maureen D Toomey; Julie Falardeau; John R Samples; John T Vetto
Journal:  Breast Cancer Res Treat       Date:  2007-01-27       Impact factor: 4.872

7.  Serum concentrations of tamoxifen and its metabolites increase with age during steady-state treatment.

Authors:  Ernst A Lien; Håvard Søiland; Steinar Lundgren; Turid Aas; Vidar M Steen; Gunnar Mellgren; Jennifer Gjerde
Journal:  Breast Cancer Res Treat       Date:  2013-09-01       Impact factor: 4.872

8.  The active tamoxifen metabolite endoxifen (4OHNDtam) strongly down-regulates cytokeratin 6 (CK6) in MCF-7 breast cancer cells.

Authors:  Thomas Helland; Jennifer Gjerde; Simon Dankel; Ingvild S Fenne; Linn Skartveit; Andreas Drangevåg; Olivera Bozickovic; Marianne Hauglid Flågeng; Håvard Søiland; Gunnar Mellgren; Ernst A Lien
Journal:  PLoS One       Date:  2015-04-13       Impact factor: 3.240

9.  Tissue distribution of 4-hydroxy-N-desmethyltamoxifen and tamoxifen-N-oxide.

Authors:  Jennifer Gjerde; Sara Gandini; Aliana Guerrieri-Gonzaga; Line L Haugan Moi; Valentina Aristarco; Gunnar Mellgren; Andrea Decensi; Ernst A Lien
Journal:  Breast Cancer Res Treat       Date:  2012-05-05       Impact factor: 4.872

10.  Risk of Endometrial Cancer and Frequencies of Invasive Endometrial Procedures in Young Breast Cancer Survivors Treated With Tamoxifen: A Nationwide Study.

Authors:  Soojeong Choi; Young Jae Lee; Jae Ho Jeong; Jinhong Jung; Jong Won Lee; Hee Jeong Kim; Beom Seok Ko; Byung Ho Son; Sei Hyun Ahn; Yura Lee; Il Yong Chung
Journal:  Front Oncol       Date:  2021-06-03       Impact factor: 6.244

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