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Aromatase inhibitors use and risk for cardiovascular disease in breast cancer patients: a population-based cohort study

Aromatase inhibitors use and risk for cardiovascular disease in breast cancer patients: a population-based cohort study
Aromatase inhibitors use and risk for cardiovascular disease in breast cancer patients: a population-based cohort study
Background: prior studies regarding use of Aromatase inhibitors (AIs) and risk for cardiovascular disease (CVD) have shown conflicting results. This retrospective cohort study aimed to investigate whether AIs use affects risk for CVD events in postmenopausal breast cancer survivors.

Methods: using a retrospective cohort study design, four CVD outcomes; heart failure or cardiomyopathy, arrhythmia, acute ischemic heart disease and ischemic stroke or Transient Ischemic Attack were compared with uni- and multivariate Cox regression analyses according to exposure to endocrine therapy (use of AI, tamoxifen or AI/tamoxifen sequentially) or no endocrine therapy.

Results: in total 15815 postmenopausal women, surgically treated to early breast cancer during 2006–2012, were included. No significantly increased risk for CVD events was observed in patients with AI use in the whole cohort. However, two subgroup analyses showed increased risk for CVD events in the AI/tamoxifen sequential group; heart failure in patients older than 75 years (Hazard Ratio (HR) 2.44; 95% Confidence Interval (CI): 1.32–4.54) and arrhythmia in patients without prior CVD (HR 1.45; 95% CI: 1.01–2.10). An increased risk for arrhythmia and acute ischemic heart disease in patients with at least four years of AI treatment compared with no or short-time exposure was observed (HR 2.12; 95% CI: 1.40–3.25 for arrhythmia; HR 2.03; 95% CI: 1.15–3.58 for ischemic heart disease).

Conclusion: our results indicate an increased risk for ischemic heart disease and arrhythmia in patients treated for more than four years with AIs. This should be considered in the risk-benefit assessment concerning endocrine therapy.
0960-9776
157-164
Sund, Maria
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Garcia-Argibay, Miguel
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Garmo, Hans
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Ahlgren, Johan
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Wennstig, Anna-Karin
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Fredriksson, Irma
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Lindman, Henrik
cd42159a-c67a-43a9-b20f-609d371315e5
Valachis, Antonis
ba747695-6e62-4cef-9c61-13d83eadca48
Sund, Maria
b099f674-da3c-4762-ab41-d35ec7f1632c
Garcia-Argibay, Miguel
e5a6941e-4dcc-401a-9de4-09557c8856ef
Garmo, Hans
c64d499e-fa52-40f6-863a-802f0b150883
Ahlgren, Johan
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Wennstig, Anna-Karin
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Fredriksson, Irma
712e4f6a-0c4a-4a82-8a10-499ee24a6e91
Lindman, Henrik
cd42159a-c67a-43a9-b20f-609d371315e5
Valachis, Antonis
ba747695-6e62-4cef-9c61-13d83eadca48

Sund, Maria, Garcia-Argibay, Miguel, Garmo, Hans, Ahlgren, Johan, Wennstig, Anna-Karin, Fredriksson, Irma, Lindman, Henrik and Valachis, Antonis (2021) Aromatase inhibitors use and risk for cardiovascular disease in breast cancer patients: a population-based cohort study. The Breast, 59, 157-164. (doi:10.1016/j.breast.2021.07.004).

Record type: Article

Abstract

Background: prior studies regarding use of Aromatase inhibitors (AIs) and risk for cardiovascular disease (CVD) have shown conflicting results. This retrospective cohort study aimed to investigate whether AIs use affects risk for CVD events in postmenopausal breast cancer survivors.

Methods: using a retrospective cohort study design, four CVD outcomes; heart failure or cardiomyopathy, arrhythmia, acute ischemic heart disease and ischemic stroke or Transient Ischemic Attack were compared with uni- and multivariate Cox regression analyses according to exposure to endocrine therapy (use of AI, tamoxifen or AI/tamoxifen sequentially) or no endocrine therapy.

Results: in total 15815 postmenopausal women, surgically treated to early breast cancer during 2006–2012, were included. No significantly increased risk for CVD events was observed in patients with AI use in the whole cohort. However, two subgroup analyses showed increased risk for CVD events in the AI/tamoxifen sequential group; heart failure in patients older than 75 years (Hazard Ratio (HR) 2.44; 95% Confidence Interval (CI): 1.32–4.54) and arrhythmia in patients without prior CVD (HR 1.45; 95% CI: 1.01–2.10). An increased risk for arrhythmia and acute ischemic heart disease in patients with at least four years of AI treatment compared with no or short-time exposure was observed (HR 2.12; 95% CI: 1.40–3.25 for arrhythmia; HR 2.03; 95% CI: 1.15–3.58 for ischemic heart disease).

Conclusion: our results indicate an increased risk for ischemic heart disease and arrhythmia in patients treated for more than four years with AIs. This should be considered in the risk-benefit assessment concerning endocrine therapy.

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Accepted/In Press date: 6 July 2021
e-pub ahead of print date: 7 July 2021
Published date: 12 July 2021

Identifiers

Local EPrints ID: 488766
URI: http://eprints.soton.ac.uk/id/eprint/488766
ISSN: 0960-9776
PURE UUID: cbd5b914-f6ba-4b39-bcd1-a1cc5d692cb5
ORCID for Miguel Garcia-Argibay: ORCID iD orcid.org/0000-0002-4811-2330

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Date deposited: 05 Apr 2024 16:37
Last modified: 10 Apr 2024 02:15

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Contributors

Author: Maria Sund
Author: Miguel Garcia-Argibay ORCID iD
Author: Hans Garmo
Author: Johan Ahlgren
Author: Anna-Karin Wennstig
Author: Irma Fredriksson
Author: Henrik Lindman
Author: Antonis Valachis

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