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Endocrine regimen and early subclinical atherosclerosis in premenopausal HR+/HER2- breast cancer: real-world evidence and regimen-dependent effects of Sanhuang Decoction.

Frontiers in oncology 2026 Vol.16() p. 1695776

Hong K, Wang C, Yang M, Du M, Wang H, Wu J, Liu X, Li X, Wu W, Li S, Cheng H, Yao C

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[INTRODUCTION] Adjuvant endocrine therapy for hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer improves survival but may worsen cardiometabolic he

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  • 표본수 (n) 95
  • 95% CI -0.090 to -0.003

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BibTeX ↓ RIS ↓
APA Hong K, Wang C, et al. (2026). Endocrine regimen and early subclinical atherosclerosis in premenopausal HR+/HER2- breast cancer: real-world evidence and regimen-dependent effects of Sanhuang Decoction.. Frontiers in oncology, 16, 1695776. https://doi.org/10.3389/fonc.2026.1695776
MLA Hong K, et al.. "Endocrine regimen and early subclinical atherosclerosis in premenopausal HR+/HER2- breast cancer: real-world evidence and regimen-dependent effects of Sanhuang Decoction.." Frontiers in oncology, vol. 16, 2026, pp. 1695776.
PMID 41684590

Abstract

[INTRODUCTION] Adjuvant endocrine therapy for hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer improves survival but may worsen cardiometabolic health; the cardiovascular impact of aromatase inhibitor plus ovarian function suppression (AI+OFS) in premenopausal women remains unclear. We compared endocrine regimens on subclinical atherosclerosis and 24-month lipid trajectories and explored potential modulatory effects of Sanhuang Decoction (SHD).

[METHODS] In this retrospective cohort of 280 HR+/HER2- patients, initial endocrine therapy was AI+OFS (n = 95), tamoxifen (TAM; n = 141), or TAM+OFS (n = 44). Lipid profiles (total cholesterol, triglycerides, low-density lipoprotein cholesterol [LDL-C], high-density lipoprotein cholesterol [HDL-C]) were analyzed using mixed-effects models adjusted for cardiometabolic and treatment covariates. New-onset or worsening fatty liver, new-onset carotid plaque, and initiation of lipid-lowering therapy were evaluated with Kaplan-Meier and Cox models.

[RESULTS] In adjusted mixed-effects models, AI+OFS versus TAM was associated with higher LDL-C (β 0.088 mmol/L; 95% confidence interval [CI] 0.013-0.163) and lower HDL-C (β -0.046 mmol/L; 95% CI -0.090 to -0.003), whereas total cholesterol and triglycerides did not differ between regimens. Incidences of fatty liver, carotid plaque, and initiation of lipid-lowering therapy varied across groups, but most adjusted Cox models showed no significant regimen effects. AI+OFS showed a trend toward a higher hazard of new-onset carotid plaque versus TAM (hazard ratio [HR] 3.09; 95% CI 0.96-9.93), and higher baseline glycated hemoglobin predicted earlier initiation of lipid-lowering therapy (HR 2.54; 95% CI 1.29-4.99). In exploratory interaction analyses, among SHD users TAM+OFS versus TAM was associated with lower LDL-C and total cholesterol, whereas in AI+OFS versus TAM SHD use was associated with lower HDL-C.

[CONCLUSION] In premenopausal women with HR+/HER2- breast cancer, AI+OFS was associated with an adverse lipid profile and a possible increase in carotid plaque compared with TAM-based regimens. Regimen-dependent associations between SHD and lipid profiles support individualized cardiovascular monitoring and cautious use of adjunctive SHD in this population.

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