Abstract
Purpose
This meta-analysis investigated the association between the risk of breast cancer and hormone replacement therapy (HRT). Various stratified analyses were performed according to race (Asian/Westerner), HRT type [all hormone therapies, estrogen-only therapy (ET), or combined estrogen–progestin therapy (EPT)], histological breast cancer type (ductal/lobular/mixed ductal–lobular), and estrogen receptor status (ER-positive/ER-negative).
Methods
A literature search was performed using Pubmed, Embase, and KoreaMed. Twenty-five epidemiological studies including 23 cohort studies and two randomized controlled trials were included in this meta-analysis.
Results
Using a random-effects model, HRT use was found to be positively associated with the risk of breast cancer with a pooled hazard ratio (HR) of 1.33 [95% confidence interval (CI) 1.24, 1.44]. Compared with ET, EPT was more strongly associated with breast cancer risk. EPT was associated with both ductal and lobular breast cancer risks [for ductal breast cancer, HR = 1.51 (95% CI 1.28, 1.78); for lobular breast cancer, HR = 1.38 (95% CI 1.20, 1.60)]. According to ER status, all HRTs were associated with the risk of ER-positive breast cancer, but not with that of ER-negative breast cancer.
Conclusions
Asian HRT users had a higher risk of breast cancer than western HRT users. Both ET and EPT were significantly associated with the risk of all breast cancer histological types and ER-positive breast cancer.
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Abbreviations
- CI:
-
Confidence interval
- EGF:
-
Epidermal growth factor
- EPT:
-
Combined estrogen–progestin therapy
- ER:
-
Estrogen receptor
- ET:
-
Estrogen-only therapy
- Her2/neu:
-
Human epidermal growth factor receptor-2
- HR:
-
Hazard ratio
- HRT:
-
Hormone replacement therapy
- IGF:
-
Insulin-like growth factor
- RR:
-
Risk ratio
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Kim, S., Ko, Y., Lee, H.J. et al. Menopausal hormone therapy and the risk of breast cancer by histological type and race: a meta-analysis of randomized controlled trials and cohort studies. Breast Cancer Res Treat 170, 667–675 (2018). https://doi.org/10.1007/s10549-018-4782-2
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DOI: https://doi.org/10.1007/s10549-018-4782-2