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Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis

PURPOSE: Thromboembolism is a common adverse event in women treated with tamoxifen (TAM) for breast cancer. The risk in male breast cancer patients is poorly investigated. We aimed to examine the risk of thrombotic events after TAM in male breast cancer patients. PATIENTS AND METHODS: In this prospe...

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Autores principales: Eggemann, Holm, Bernreiter, Anna-Lena, Reinisch, Mattea, Loibl, Sibylle, Taran, Florin-Andrei, Costa, Serban-Dan, Ignatov, Atanas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353985/
https://www.ncbi.nlm.nih.gov/pubmed/30655614
http://dx.doi.org/10.1038/s41416-018-0369-2
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author Eggemann, Holm
Bernreiter, Anna-Lena
Reinisch, Mattea
Loibl, Sibylle
Taran, Florin-Andrei
Costa, Serban-Dan
Ignatov, Atanas
author_facet Eggemann, Holm
Bernreiter, Anna-Lena
Reinisch, Mattea
Loibl, Sibylle
Taran, Florin-Andrei
Costa, Serban-Dan
Ignatov, Atanas
author_sort Eggemann, Holm
collection PubMed
description PURPOSE: Thromboembolism is a common adverse event in women treated with tamoxifen (TAM) for breast cancer. The risk in male breast cancer patients is poorly investigated. We aimed to examine the risk of thrombotic events after TAM in male breast cancer patients. PATIENTS AND METHODS: In this prospective cohort study, 448 patients treated between May 2009 and July 2017 for male breast cancer (BC) were assessed for eligibility. Patients with follow-up shorter than 6 months were excluded. The cumulative risk of thromboembolism was evaluated. RESULTS: The median follow-up was 47 months (range 6–101 months) with a median age of 69.4 years (range 27–89 years). Oestrogen receptor and progesterone receptor expression levels were observed in 98.3 and 94.9% of cases, respectively. During the follow-up period, thrombotic events were documented in 21 (11.9%) of 177 patients receiving TAM and in 1 (2.5%) of 41 patients who did not receive tamoxifen. The estimated incidence was 51.9 per 1000 person-years and 21.5 per 1000 person-years, respectively. Notably, the highest risk was identified in the first 18 months, where 81% of the observed thrombotic events occurred. Patients aged older than 71 years had a significantly increased risk of thrombotic event under TAM treatment than their younger counterparts (p = 0.033). History of thrombotic event, cardiovascular and liver disease, as well as additional adjuvant treatment were not associated with increased thrombotic risk. CONCLUSION: The risk of thrombotic event in men treated with TAM for breast cancer is markedly increased in the first 18 months of treatment, and should be considered during treatment decisions.
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spelling pubmed-63539852020-01-17 Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis Eggemann, Holm Bernreiter, Anna-Lena Reinisch, Mattea Loibl, Sibylle Taran, Florin-Andrei Costa, Serban-Dan Ignatov, Atanas Br J Cancer Article PURPOSE: Thromboembolism is a common adverse event in women treated with tamoxifen (TAM) for breast cancer. The risk in male breast cancer patients is poorly investigated. We aimed to examine the risk of thrombotic events after TAM in male breast cancer patients. PATIENTS AND METHODS: In this prospective cohort study, 448 patients treated between May 2009 and July 2017 for male breast cancer (BC) were assessed for eligibility. Patients with follow-up shorter than 6 months were excluded. The cumulative risk of thromboembolism was evaluated. RESULTS: The median follow-up was 47 months (range 6–101 months) with a median age of 69.4 years (range 27–89 years). Oestrogen receptor and progesterone receptor expression levels were observed in 98.3 and 94.9% of cases, respectively. During the follow-up period, thrombotic events were documented in 21 (11.9%) of 177 patients receiving TAM and in 1 (2.5%) of 41 patients who did not receive tamoxifen. The estimated incidence was 51.9 per 1000 person-years and 21.5 per 1000 person-years, respectively. Notably, the highest risk was identified in the first 18 months, where 81% of the observed thrombotic events occurred. Patients aged older than 71 years had a significantly increased risk of thrombotic event under TAM treatment than their younger counterparts (p = 0.033). History of thrombotic event, cardiovascular and liver disease, as well as additional adjuvant treatment were not associated with increased thrombotic risk. CONCLUSION: The risk of thrombotic event in men treated with TAM for breast cancer is markedly increased in the first 18 months of treatment, and should be considered during treatment decisions. Nature Publishing Group UK 2019-01-17 2019-02-05 /pmc/articles/PMC6353985/ /pubmed/30655614 http://dx.doi.org/10.1038/s41416-018-0369-2 Text en © Cancer Research UK 2019 https://creativecommons.org/licenses/by/4.0/This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Eggemann, Holm
Bernreiter, Anna-Lena
Reinisch, Mattea
Loibl, Sibylle
Taran, Florin-Andrei
Costa, Serban-Dan
Ignatov, Atanas
Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title_full Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title_fullStr Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title_full_unstemmed Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title_short Tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
title_sort tamoxifen treatment for male breast cancer and risk of thromboembolism: prospective cohort analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353985/
https://www.ncbi.nlm.nih.gov/pubmed/30655614
http://dx.doi.org/10.1038/s41416-018-0369-2
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