Low-dose aspirin, statins, and metformin and survival in patients with breast cancers: a Norwegian population-based cohort study.

L Lukas Löfling, Nathalie C Støer, Bettina Kulle Andreassen, Giske Ursin, Edoardo Botteri
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Abstract

Background: Previous studies assessed the prognostic effect of aspirin, statins, and metformin in breast cancer (BC) patients, with inconclusive results.

Methods: We performed a nationwide population-based cohort study to evaluate if post-diagnostic use of low-dose aspirin, statins, and metformin was associated with BC-specific survival. Women aged ≥ 50 years and diagnosed with BC in 2004-2017, who survived ≥ 12 months after diagnosis (follow-up started 12 months after diagnosis), were identified in the Cancer Registry of Norway. The Norwegian Prescription Database provided information on prescriptions. Multivariable Cox proportional hazard models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI) for the association between post-diagnostic use and BC-specific survival, overall and by oestrogen receptor (ER) status.

Results: A total of 26,190 patients were included. Of these, 5324 (20%), 7591 (29%), and 1495 (6%) were post-diagnostic users of low-dose aspirin, statins, and metformin, respectively. The median follow-up was 6.1 years, and 2169 (8%) patients died from BC. HRs for use, compared to no use, were estimated at 0.96 (95% CI 0.85-1.08) for low-dose aspirin (ER+: HR = 0.97, 95% CI 0.83-1.13; ER-: HR = 0.97, 95% CI 0.73-1.29, p value for interaction = 0.562), 0.84 (95% CI 0.75-0.94) for statins (ER+: HR = 0.95, 95% CI 0.82-1.09; ER-: HR = 0.77, 95% CI 0.60-1.00, p value for interaction = 0.259), and 0.70 (95% CI 0.51-0.96) for metformin (compared to use of non-metformin antidiabetics) (ER+: HR = 0.67, 95% CI 0.45-1.01; ER-: HR = 1.62, 95% CI 0.72-3.62, p value for interaction = 0.077).

Conclusion: We found evidence supporting an association between post-diagnostic use of statins and metformin and survival, in patients with BC. Our findings indicate potential differences according to ER status.

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低剂量阿司匹林、他汀类药物和二甲双胍对乳腺癌患者生存率的影响:一项基于挪威人群的队列研究
背景:先前的研究评估了阿司匹林、他汀类药物和二甲双胍对乳腺癌(BC)患者的预后影响,但结果不确定。方法:我们进行了一项基于全国人群的队列研究,以评估诊断后使用低剂量阿司匹林、他汀类药物和二甲双胍是否与bc特异性生存率相关。年龄≥50岁并在2004-2017年诊断为BC的女性,在诊断后存活≥12个月(诊断后12个月开始随访),在挪威癌症登记处确定。挪威处方数据库提供了关于处方的资料。使用多变量Cox比例风险模型来估计诊断后使用与bc特异性生存、总体和雌激素受体(ER)状态之间的关联的风险比(HR)和95%置信区间(CI)。结果:共纳入26190例患者。其中,5324例(20%)、7591例(29%)和1495例(6%)分别是诊断后使用低剂量阿司匹林、他汀类药物和二甲双胍的患者。中位随访时间为6.1年,2169例(8%)患者死于BC。与不使用相比,低剂量阿司匹林的使用HR估计为0.96 (95% CI 0.85-1.08) (ER+: HR = 0.97, 95% CI 0.83-1.13;他汀类药物ER-: HR = 0.97, 95% CI 0.73-1.29,相互作用p值= 0.562),0.84 (95% CI 0.75-0.94) (ER+: HR = 0.95, 95% CI 0.82-1.09;二甲双胍的ER-: HR = 0.77, 95% CI 0.60-1.00,相互作用的p值= 0.259)和0.70 (95% CI 0.51-0.96)(与使用非二甲双胍降糖药相比)(ER+: HR = 0.67, 95% CI 0.45-1.01;ER-: HR = 1.62, 95% CI = 0.72-3.62,交互作用的p值= 0.077)。结论:我们发现证据支持BC患者诊断后使用他汀类药物和二甲双胍与生存率之间的关联。我们的研究结果表明,不同的ER状态可能存在差异。
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