Association between Menopausal Hormone Therapy and Cancer: A Nationwide Retrospective Cohort Study in South Korea.
[BACKGROUND] To investigate menopausal hormone therapy's (MHT) overall cancer risks in postmenopausal women.
- 95% CI 1.119-1.227
- 연구 설계 cohort study
APA
Yuk JS, Kim BS, et al. (2026). Association between Menopausal Hormone Therapy and Cancer: A Nationwide Retrospective Cohort Study in South Korea.. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 35(4), 569-577. https://doi.org/10.1158/1055-9965.EPI-25-1429
MLA
Yuk JS, et al.. "Association between Menopausal Hormone Therapy and Cancer: A Nationwide Retrospective Cohort Study in South Korea.." Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, vol. 35, no. 4, 2026, pp. 569-577.
PMID
41591384
Abstract
[BACKGROUND] To investigate menopausal hormone therapy's (MHT) overall cancer risks in postmenopausal women.
[METHODS] This retrospective cohort study used South Korea's National Health Insurance System data, focusing on women aged 40 or older diagnosed with initial menopause (2011-2014), comparing an MHT group (≥6 months) with a propensity score-matched non-MHT group for cancer incidence until 2020.
[RESULTS] We matched 138,445 women per group, followed for a median of 7.9 years. Breast (28%), thyroid (23%), and colorectal (8%) cancers predominated. MHT increased the overall cancer risk [hazard ratio (HR) 1.104; 95% confidence interval (CI), 1.064-1.145], especially estrogen plus progestogen therapy (EPT; HR, 1.172; 95% CI, 1.119-1.227) and estrogen-alone therapy (ET; HR, 1.142; 95% CI, 1.05-1.244), but not tibolone. Breast (HR, 1.568; 95% CI, 1.448-1.697), colorectal (HR, 1.157; 95% CI, 1.018-1.315), brain (HR, 1.618; 95% CI, 1.6-2.258), and renal (HR, 1.378; 95% CI, 1.053-1.803) cancers were more common in MHT; uterine cancer decreased (HR, 0.865; 95% CI, 0.763-0.981).
[CONCLUSIONS] MHT increased overall cancer risk, with EPT and ET elevating risks, unlike tibolone. MHT users faced higher risks of breast, brain, renal, and colorectal cancers but a lower risk of uterine cancer.
[IMPACT] These findings suggest considering lower-potency progestogens in current estrogen/progestogen therapy. This change might increase endometrial cancer risk but reduce breast cancer risk, potentially lowering overall cancer risk.
[METHODS] This retrospective cohort study used South Korea's National Health Insurance System data, focusing on women aged 40 or older diagnosed with initial menopause (2011-2014), comparing an MHT group (≥6 months) with a propensity score-matched non-MHT group for cancer incidence until 2020.
[RESULTS] We matched 138,445 women per group, followed for a median of 7.9 years. Breast (28%), thyroid (23%), and colorectal (8%) cancers predominated. MHT increased the overall cancer risk [hazard ratio (HR) 1.104; 95% confidence interval (CI), 1.064-1.145], especially estrogen plus progestogen therapy (EPT; HR, 1.172; 95% CI, 1.119-1.227) and estrogen-alone therapy (ET; HR, 1.142; 95% CI, 1.05-1.244), but not tibolone. Breast (HR, 1.568; 95% CI, 1.448-1.697), colorectal (HR, 1.157; 95% CI, 1.018-1.315), brain (HR, 1.618; 95% CI, 1.6-2.258), and renal (HR, 1.378; 95% CI, 1.053-1.803) cancers were more common in MHT; uterine cancer decreased (HR, 0.865; 95% CI, 0.763-0.981).
[CONCLUSIONS] MHT increased overall cancer risk, with EPT and ET elevating risks, unlike tibolone. MHT users faced higher risks of breast, brain, renal, and colorectal cancers but a lower risk of uterine cancer.
[IMPACT] These findings suggest considering lower-potency progestogens in current estrogen/progestogen therapy. This change might increase endometrial cancer risk but reduce breast cancer risk, potentially lowering overall cancer risk.
MeSH Terms
Humans; Female; Retrospective Studies; Republic of Korea; Middle Aged; Aged; Neoplasms; Adult; Incidence; Hormone Replacement Therapy; Estrogen Replacement Therapy; Risk Factors; Progestins; Menopause; Breast Neoplasms
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