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


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
02 2019
Historique:
received: 11 09 2018
accepted: 05 12 2018
revised: 02 12 2018
pubmed: 19 1 2019
medline: 13 11 2019
entrez: 19 1 2019
Statut: ppublish

Résumé

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. 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. 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. 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.

Identifiants

pubmed: 30655614
doi: 10.1038/s41416-018-0369-2
pii: 10.1038/s41416-018-0369-2
pmc: PMC6353985
doi:

Substances chimiques

Tamoxifen 094ZI81Y45

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

301-305

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Auteurs

Holm Eggemann (H)

Department of Obstetrics and Gynaecology, Otto-von-Guericke University, Magdeburg, Germany. holm.eggemann@med.ovgu.de.

Anna-Lena Bernreiter (AL)

Department of Obstetrics and Gynaecology, Otto-von-Guericke University, Magdeburg, Germany.

Mattea Reinisch (M)

Breast Unit, Kliniken Essen-Mitte, Essen, Germany.

Sibylle Loibl (S)

GBG Forschungs GmbH, Neu-Isenburg, Germany.

Florin-Andrei Taran (FA)

Department of Obstetrics and Gynaecology, University Hospital Tübingen, Tübingen, Germany.

Serban-Dan Costa (SD)

Department of Obstetrics and Gynaecology, Otto-von-Guericke University, Magdeburg, Germany.

Atanas Ignatov (A)

Department of Obstetrics and Gynaecology, Otto-von-Guericke University, Magdeburg, Germany. atanas.ignatov@gmail.com.
Department of Gynaecology and Obstetrics, University Medical Center, Regensburg, Germany. atanas.ignatov@gmail.com.

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Classifications MeSH