Department of Research, Cancer Registry of Norway, Postboks 5313 Majorstuen, 0304, Oslo, Norway.
Cancer Registry of Norway, Oslo, Norway.
Breast Cancer Res. 2023 Aug 30;25(1):101. doi: 10.1186/s13058-023-01697-2.
Previous studies assessed the prognostic effect of aspirin, statins, and metformin in breast cancer (BC) patients, with inconclusive results.
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.
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).
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.
先前的研究评估了阿司匹林、他汀类药物和二甲双胍在乳腺癌(BC)患者中的预后作用,但结果不一致。
我们进行了一项全国范围内的基于人群的队列研究,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 特异性生存相关。在挪威癌症登记处中,纳入了 2004 年至 2017 年年龄≥50 岁且被诊断为 BC 并在诊断后存活≥12 个月(随访从诊断后 12 个月开始)的女性。挪威处方数据库提供了处方信息。多变量 Cox 比例风险模型用于估计诊断后使用与 BC 特异性生存之间的关联的风险比(HR)和 95%置信区间(CI),整体和根据雌激素受体(ER)状态进行分析。
共纳入 26190 名患者。其中,5324 名(20%)、7591 名(29%)和 1495 名(6%)患者分别为诊断后低剂量阿司匹林、他汀类药物和二甲双胍的使用者。中位随访时间为 6.1 年,2169 名(8%)患者死于 BC。与未使用者相比,低剂量阿司匹林(ER+:HR=0.97,95%CI 0.83-1.13;ER-:HR=0.97,95%CI 0.73-1.29,p 值为交互作用=0.562)、他汀类药物(ER+:HR=0.95,95%CI 0.82-1.09;ER-:HR=0.77,95%CI 0.60-1.00,p 值为交互作用=0.259)和二甲双胍(与使用非二甲双胍类降糖药相比)(HR=0.70,95%CI 0.51-0.96)的 HR 分别估计为 0.96(95%CI 0.85-1.08)、0.84(95%CI 0.75-0.94)。
我们发现了支持诊断后使用他汀类药物和二甲双胍与 BC 患者生存相关的证据。我们的研究结果表明,根据 ER 状态可能存在差异。