4.5 Article

Adjuvant endocrine therapy in patients with estrogen receptor-low positive breast cancer: A prospective cohort study

期刊

BREAST
卷 66, 期 -, 页码 89-96

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CHURCHILL LIVINGSTONE
DOI: 10.1016/j.breast.2022.09.008

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Breast cancer; Estrogen receptor low-positive; Endocrine therapy; Aromatase inhibitor; Survival

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The study found that AI/T + AI combination endocrine therapy may be a reasonable treatment option for ER-low positive breast cancer patients, and treatment duration of more than 3 years is associated with better disease-free survival.
Background: Little is known about the benefits of adjuvant endocrine therapy (ET) in low ER-positive breast cancer (1%-10%) patients. We analyzed the association between ET and breast cancer-specific survival (BCSS) in these patients with respect to the regimen and the duration of ET.Methods: Patients were classified into three groups based on the regimen and duration of ET. The regimens included aromatase inhibitor (AI) monotherapy or sequential tamoxifen followed by an AI (AI/T + AI), or only tamoxifen and no ET. The duration of ET included 2-3 years and >3 years. Multivariate Cox regression analysis was employed to calculate the hazard ratios (HRs) with 95% confidence intervals (CIs).Results: Of the 10,696 patients diagnosed with breast cancer between 2010 and 2020, 407 women were identified with ER-low positive disease and met the inclusion criteria. During a median follow-up of 5.2 years, patients who received ET improved BCSS. Of them, those with AI/T + AI had increased BCSS compared to patients without ET, after adjusting for demographics and tumor characteristics, especially in ER-low/HER-2-positive breast cancer. After additional adjustment for treatment mode, the association maintained a similar trend. Patients who received >3 years of ET was associated with a better DFS. There was no significant difference in BCSS between patients with 2-3 years and >3 years of ET.Conclusion: For ER-low patients, findings suggest that ET with AI/T + AI may be a reasonable treatment alter-native. This effect should be assessed in randomized studies.

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