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芳香化酶抑制剂治疗与绝经后乳腺癌患者的严重骨质疏松性骨折风险:一项全国性真实世界队列研究

Aromatase inhibitors therapy and major osteoporotic fracture risk in postmenopausal breast cancer patients: a nationwide real-world cohort study.

作者信息

Liu Pin-Han, Tsai Ching-Fang, Hsu Yu-Chen, Wu Cheng-Yi, Yang Hsin-Yi

机构信息

Division of Plastic Surgery, Department of Surgery, Chia-Yi Christian Hospital, Chiayi City, Taiwan.

Clinical Data Center, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi City, Taiwan.

出版信息

Breast Cancer Res. 2025 May 30;27(1):95. doi: 10.1186/s13058-025-02050-5.

Abstract

BACKGROUND

The increased risk of fractures associated with aromatase inhibitors (AIs) therapy has been well established in clinical trials; however, data on Asian populations remain limited. Furthermore, the impact of AIs on fracture risk across different age groups and breast cancer stages has not been thoroughly investigated. This study aimed to assess the association between AIs therapy and major osteoporotic fractures (MOFs) in postmenopausal Taiwanese women with breast cancer using real-world data.

METHODS

We used Taiwan’s National Health Insurance and Cancer Registry databases to identify women aged  50 years with newly diagnosed breast cancer who received continuous AIs ( = 1,835) or tamoxifen (TAM) ( = 1,868) treatment. MOFs requiring hospitalization were tracked through 2019. The mean follow-up duration was 47.49 months (SD = 29.73) for the AIs group and 72.49 months (SD = 37.22) for the TAM group. Cox regression analysis was used to estimate hazard ratios (HRs) with 95% confidence intervals (CIs). MOFs incidence in AIs users compared to TAM users, with secondary outcomes including fractures of the spine, hip, humerus, and forearm.

RESULTS

AIs users had a higher incidence of MOFs than TAM users. After adjustment, AIs therapy significantly increased forearm fracture risk [adjusted hazard ratios (aHR) = 2.16, 95% CI = 1.24–3.76)]. In age-stratified analyses, women aged 50–65 years had a notably higher risk of hip fractures (aHR = 5.65, 95% CI: 1.55–20.68) and forearm fractures (aHR = 3.14, 95% CI: 1.55–6.36) compared with TAM users, while no significant difference was observed in women over 65 years. Among early-stage (0–1) patients, AIs use was associated with a higher risk of hip fractures (aHR = 3.14, 95% CI: 1.10–8.97). In later-stage (2–3) patients, AIs use was linked to a higher risk of forearm fractures (aHR = 2.41, 95% CI: 1.11–5.20). Additionally, even among low-risk groups, AIs users had a significantly higher fracture risk than TAM users ( = 0.040).

CONCLUSION

AIs therapy significantly increased the risk of hip and forearm fractures compared to TAM, particularly in women aged 50–65 years and in specific cancer stages. Regular bone mineral density monitoring and personalized bone-protective strategies are recommended.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1186/s13058-025-02050-5.

摘要

背景

芳香化酶抑制剂(AIs)治疗相关的骨折风险增加在临床试验中已得到充分证实;然而,关于亚洲人群的数据仍然有限。此外,AIs对不同年龄组和乳腺癌分期骨折风险的影响尚未得到充分研究。本研究旨在利用真实世界数据评估台湾绝经后乳腺癌女性中AIs治疗与主要骨质疏松性骨折(MOFs)之间的关联。

方法

我们使用台湾国民健康保险和癌症登记数据库,确定年龄≥50岁、新诊断为乳腺癌且接受持续AIs(n = 1835)或他莫昔芬(TAM)(n = 1868)治疗的女性。通过2019年追踪需要住院治疗的MOFs。AIs组的平均随访时间为47.49个月(标准差 = 29.73),TAM组为72.49个月(标准差 = 37.22)。采用Cox回归分析估计风险比(HRs)及95%置信区间(CIs)。比较AIs使用者与TAM使用者的MOFs发生率,次要结局包括脊柱、髋部、肱骨和前臂骨折。

结果

AIs使用者的MOFs发生率高于TAM使用者。调整后,AIs治疗显著增加前臂骨折风险[调整后风险比(aHR)= 2.16,95% CI = 1.24 - 3.76]。在年龄分层分析中,50 - 65岁的女性与TAM使用者相比,髋部骨折(aHR = 5.65,95% CI:1.55 - 20.68)和前臂骨折(aHR = 3.14,95% CI:1.55 - 6.36)风险显著更高,而65岁以上女性未观察到显著差异。在早期(0 - 1期)患者中,使用AIs与髋部骨折风险较高相关(aHR = 3.14,95% CI:1.10 - 8.97)。在晚期(2 - 3期)患者中,使用AIs与前臂骨折风险较高相关(aHR = 2.41,95% CI:1.11 - 5.20)。此外,即使在低风险组中,AIs使用者的骨折风险也显著高于TAM使用者(P = 0.040)。

结论

与TAM相比,AIs治疗显著增加髋部和前臂骨折风险,特别是在50 - 65岁女性和特定癌症分期中。建议定期进行骨密度监测并采取个性化的骨保护策略。

补充信息

在线版本包含可在10.1186/s13058 - 025 - 02050 - 5获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e86/12125836/82fd6763d174/13058_2025_2050_Fig1_HTML.jpg

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