Acetyl Salicylic Acid, COX-2 Inhibitors and Other NSAIDs and Breast Cancer Survival in a Finnish Population-Based Cohort

IF 1.5 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-07-05 DOI:10.1002/cnr2.70271
M. Malin, M. Murto, O. Arponen, A. Jukkola, A. Siltari, M. Artama, K. Visvanathan, T. Murtola
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Abstract

Background

Non-steroidal anti-inflammatory drugs (NSAIDs), particularly acetylsalicylic acid (ASA), have been associated with reduced breast cancer (BCa) mortality. While overexpression of cyclooxygenase-2 (COX-2) correlates with poorer prognosis in BCa, COX-2 inhibitors (coxibs) have not demonstrated a survival advantage. However, the evidence remains conflicting and limited. We examined associations between BCa mortality and NSAID use in a Finnish population-based cohort.

Methods

The study cohort, 73 170 women with new BCa diagnosis during 1995–2013 was identified from The Finnish Cancer Registry. Follow-up data including date and the cause of death, NSAID purchases from 1995 to 2015, mammography screening participation and tumor hormone receptor status, were obtained from national registries. NSAID purchases were categorized into NSAIDs overall, ASA, and coxibs. BCa-specific and overall survival by NSAID use were analyzed using Cox proportional hazard regression, adjusted for age, tumor extent, primary treatment, Charlson comorbidity index, hypertension, diabetes, mammography participation, and hormonal therapy.

Results

Pre-diagnostic use of NSAIDs (HR 0.78, 95% CI: 0.75–0.81) and coxibs (HR 0.76, 95% CI: 0.71–0.81) was associated with reduced BCa mortality, while ASA showed no association. Post-diagnostic NSAID use was associated with increased BCa mortality (HR 1.27, 95% CI: 1.22–1.33), while ASA use (HR 0.84, 95% CI: 0.73–0.97) showed dose-dependent risk reduction.

Conclusion

Post-diagnostic use of ASA is associated with reduced BCa-specific mortality, distinguishing ASA from other NSAIDs. Clinical trials are required to determine the ideal ASA dose, frequency, and duration for treating BCa. Pre-diagnostic use of NSAIDs overall is associated with a slight reduction in BCa mortality without dose dependence. The potential role of pre-diagnostic NSAID use as a prognostic factor in BCa warrants further investigation.

Abstract Image

乙酰水杨酸、COX-2抑制剂和其他非甾体抗炎药与芬兰人群的乳腺癌生存率
背景:非甾体抗炎药(NSAIDs),特别是乙酰水杨酸(ASA),与降低乳腺癌(BCa)死亡率相关。虽然环氧化酶-2 (COX-2)的过表达与BCa预后较差相关,但COX-2抑制剂(coxib)并未显示出生存优势。然而,证据仍然是相互矛盾和有限的。我们在芬兰人群为基础的队列中研究了BCa死亡率与非甾体抗炎药使用之间的关系。方法:研究队列,从芬兰癌症登记处(Finnish Cancer Registry)中确定1995-2013年期间新诊断为BCa的73 170名女性。随访数据包括死亡日期和原因、1995年至2015年购买非甾体抗炎药、乳房x光检查参与情况和肿瘤激素受体状况,均来自国家登记处。购买非甾体抗炎药分为整体非甾体抗炎药、ASA和coxib。采用Cox比例风险回归分析使用非甾体抗炎药的bca特异性和总生存率,调整年龄、肿瘤范围、初始治疗、Charlson合并症指数、高血压、糖尿病、乳房x光检查参与和激素治疗。结果诊断前使用非甾体抗炎药(HR 0.78, 95% CI: 0.75-0.81)和coxibs (HR 0.76, 95% CI: 0.71-0.81)与降低BCa死亡率相关,而ASA无相关性。诊断后使用非甾体抗炎药与BCa死亡率增加相关(HR 1.27, 95% CI: 1.22-1.33),而使用ASA (HR 0.84, 95% CI: 0.73-0.97)显示剂量依赖性风险降低。结论诊断后使用ASA与降低bca特异性死亡率相关,将ASA与其他非甾体抗炎药区分开来。需要临床试验来确定治疗BCa的理想ASA剂量、频率和持续时间。总体而言,诊断前使用非甾体抗炎药与BCa死亡率的轻微降低有关,无剂量依赖性。诊断前使用非甾体抗炎药作为BCa预后因素的潜在作用值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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