Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/42539
Title: Survival benefit of tamoxifen in male breast cancer : prospective cohort analysis
Author(s): Eggemann, HolmLook up in the Integrated Authority File of the German National Library
Brucker, CosimaLook up in the Integrated Authority File of the German National Library
Schrauder, MichaelLook up in the Integrated Authority File of the German National Library
Thill, MarcLook up in the Integrated Authority File of the German National Library
Flock, FelixLook up in the Integrated Authority File of the German National Library
Reinisch, MatteaLook up in the Integrated Authority File of the German National Library
Costa, Serban-Dan
Ignatov, AtanasLook up in the Integrated Authority File of the German National Library
Issue Date: 2020
Type: Article
Language: English
URN: urn:nbn:de:gbv:ma9:1-1981185920-444935
Subjects: Tamoxifen
Breast cancer
MBC
Disease-free survival
Abstract: Background Due to the lack of prospective data, current treatment of male breast cancer (MBC) is based on information obtained from retrospective analysis or by extrapolation from studies on female patients. In this prospectively enrolled cohort study, we retrospectively examined the survival effect of tamoxifen in MBC patients. Methods In this prospectively enrolled cohort study, 448 patients with MBC were treated between May 2009 and June 2018. The primary endpoint was disease-free survival (DFS). Results Between May 2009 and June 2018, 448 men with breast cancer were identified, with a median age at diagnosis of 69 years (range 27–96 years). The median follow-up was 39 months (range 3–89 months). Most tumours were larger than 20 mm; invasive ductal carcinoma was of no special histological type and with an intermediate grade of differentiation. Almost half of the men were diagnosed with positive axillary lymph nodes (43.5%). Hormone receptor (HR) positivity was observed in 98.4% of the patients. Notably, DFS among men who did not receive tamoxifen was significantly reduced as compared with those who underwent tamoxifen therapy (P = 0.002). The recurrence rate and mortality in the group of patients without and with tamoxifen treatment were 18.2% and 11.2%, respectively. The most common localisation of metastases was the bone. After adjustment for prognostic factors, we found that tamoxifen was found to reduce the recurrence rate by 68% (hazard ratio HR = 0.32; 95% confidence interval, CI: 0.14–0.74). Conclusions Tamoxifen treatment was associated with improved DFS for MBC patients.
URI: https://opendata.uni-halle.de//handle/1981185920/44493
http://dx.doi.org/10.25673/42539
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Sponsor/Funder: Projekt DEAL 2020
Journal Title: British journal of cancer
Publisher: Nature Publ. Group
Publisher Place: Edinburgh
Volume: 123
Issue: 1
Original Publication: 10.1038/s41416-020-0857-z
Page Start: 33
Page End: 37
Appears in Collections:Medizinische Fakultät (OA)

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