Alison J Sears, Sarah H Wild, Ines Mesa-Eguiagaray, Peter S Hall, Jonine D Figueroa
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Hazard ratios (HR) for breast cancer mortality within three years were estimated using Cox proportional hazard models, adjusting for age at breast cancer diagnosis, year of diagnosis, Scottish region, mode of detection, treatment, area-based socioeconomic status, and T2DM duration were conducted. Multiple imputation was performed as a sensitivity analysis. The distribution of molecular subtype based on St Gallen's criteria was luminal A (58%), luminal B (HER2-) (19.2%), triple negative (9.9%), luminal B (HER2 +) (8.5%), and HER2-enriched (4.4%). There were 286 breast cancer deaths in total within three years. KM estimates showed women with HER2-enriched tumours had the worst survival at ages 50 to 69, while those with triple-negative tumours had the worst survival at ages 70 to 84. Adjusted HRs (95% confidence intervals) for mortality over 3 years compared to luminal A were 2.04 (1.43, 2.90) for luminal B (HER2-), 5.68 (3.40, 9.50) for triple negative, 2.22 (1.46, 3.38) for luminal B (HER2 +), and 2.93 (1.63, 5.27) for HER2-enriched. The imputed cohort adjusted HRs were attenuated, particularly for HER2-enriched (HR = 1.71 (1.01, 2.89)) and triple negative (HR = 2.74 (1.72, 4.37)). Like the general population, triple negative and HER2-enriched tumors had worse prognosis compared to luminal A tumors and their association with breast cancer mortality are similar in women with type 2 diabetes and the general population. However, our findings revealed differences in the survival ranking of HER2-enriched and triple-negative subtypes for breast cancer diagnosed in the 50-69 age group between women with type 2 diabetes and the general population, warranting further exploration.</p>","PeriodicalId":21811,"journal":{"name":"Scientific Reports","volume":"15 1","pages":"26144"},"PeriodicalIF":3.9000,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12274475/pdf/","citationCount":"0","resultStr":"{\"title\":\"Breast cancer survival and mortality among women with type 2 diabetes: a retrospective cohort study.\",\"authors\":\"Alison J Sears, Sarah H Wild, Ines Mesa-Eguiagaray, Peter S Hall, Jonine D Figueroa\",\"doi\":\"10.1038/s41598-025-08785-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Type 2 diabetes (T2DM) is estimated to affect over 200 million women globally and over 2 million women are estimated to be diagnosed with breast cancer each year. This study aimed to determine the association between breast cancer molecular subtypes and survival in a cohort of women with T2DM. A retrospective cohort study was conducted using linked Scottish population-based data for 3,042 women diagnosed with T2DM prior to their diagnosis of invasive breast cancer between 2010 and 2019 that had complete data available. The women in the cohort were aged 50 to 84 years at the time of breast cancer diagnosis. Univariate analyses were performed using non-parametric ten-year Kaplan Meier (KM) estimates for breast cancer survival by molecular subtype. Hazard ratios (HR) for breast cancer mortality within three years were estimated using Cox proportional hazard models, adjusting for age at breast cancer diagnosis, year of diagnosis, Scottish region, mode of detection, treatment, area-based socioeconomic status, and T2DM duration were conducted. Multiple imputation was performed as a sensitivity analysis. The distribution of molecular subtype based on St Gallen's criteria was luminal A (58%), luminal B (HER2-) (19.2%), triple negative (9.9%), luminal B (HER2 +) (8.5%), and HER2-enriched (4.4%). There were 286 breast cancer deaths in total within three years. KM estimates showed women with HER2-enriched tumours had the worst survival at ages 50 to 69, while those with triple-negative tumours had the worst survival at ages 70 to 84. Adjusted HRs (95% confidence intervals) for mortality over 3 years compared to luminal A were 2.04 (1.43, 2.90) for luminal B (HER2-), 5.68 (3.40, 9.50) for triple negative, 2.22 (1.46, 3.38) for luminal B (HER2 +), and 2.93 (1.63, 5.27) for HER2-enriched. The imputed cohort adjusted HRs were attenuated, particularly for HER2-enriched (HR = 1.71 (1.01, 2.89)) and triple negative (HR = 2.74 (1.72, 4.37)). 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引用次数: 0
摘要
据估计,全球2亿多名妇女受到2型糖尿病(T2DM)的影响,每年有200多万名妇女被诊断患有乳腺癌。本研究旨在确定T2DM女性队列中乳腺癌分子亚型与生存率之间的关系。在2010年至2019年期间,对3042名在诊断为浸润性乳腺癌之前被诊断为2型糖尿病的女性进行了一项回顾性队列研究,这些女性有完整的数据可用。队列中的女性在乳腺癌诊断时年龄在50至84岁之间。采用非参数的十年Kaplan Meier (KM)对乳腺癌分子亚型生存率进行单因素分析。采用Cox比例风险模型估计三年内乳腺癌死亡率的风险比(HR),调整乳腺癌诊断年龄、诊断年份、苏格兰地区、检测方式、治疗、基于地区的社会经济状况和T2DM病程。多重输入作为敏感性分析。基于St Gallen标准的分子亚型分布为luminal A(58%)、luminal B (HER2-)(19.2%)、三阴性(9.9%)、luminal B (HER2 +)(8.5%)和HER2富集(4.4%)。三年内总共有286人死于乳腺癌。KM估计显示,患有her2富集肿瘤的女性在50至69岁之间的生存率最低,而患有三阴性肿瘤的女性在70至84岁之间的生存率最低。与luminal A相比,3年内死亡率的调整hr(95%置信区间)为:luminal B (HER2-)为2.04(1.43,2.90),三阴性为5.68 (3.40,9.50),luminal B (HER2 +)为2.22 (1.46,3.38),HER2丰富者为2.93(1.63,5.27)。输入队列调整后的HR降低,特别是her2富集(HR = 1.71(1.01, 2.89))和三阴性(HR = 2.74(1.72, 4.37))。与一般人群一样,与腔A肿瘤相比,三阴性和her2富集肿瘤的预后更差,其与乳腺癌死亡率的关联在2型糖尿病女性和一般人群中相似。然而,我们的研究结果显示,在50-69岁年龄组的2型糖尿病女性和一般人群中,诊断为乳腺癌的her2富集亚型和三阴性亚型的生存排名存在差异,值得进一步探索。
Breast cancer survival and mortality among women with type 2 diabetes: a retrospective cohort study.
Type 2 diabetes (T2DM) is estimated to affect over 200 million women globally and over 2 million women are estimated to be diagnosed with breast cancer each year. This study aimed to determine the association between breast cancer molecular subtypes and survival in a cohort of women with T2DM. A retrospective cohort study was conducted using linked Scottish population-based data for 3,042 women diagnosed with T2DM prior to their diagnosis of invasive breast cancer between 2010 and 2019 that had complete data available. The women in the cohort were aged 50 to 84 years at the time of breast cancer diagnosis. Univariate analyses were performed using non-parametric ten-year Kaplan Meier (KM) estimates for breast cancer survival by molecular subtype. Hazard ratios (HR) for breast cancer mortality within three years were estimated using Cox proportional hazard models, adjusting for age at breast cancer diagnosis, year of diagnosis, Scottish region, mode of detection, treatment, area-based socioeconomic status, and T2DM duration were conducted. Multiple imputation was performed as a sensitivity analysis. The distribution of molecular subtype based on St Gallen's criteria was luminal A (58%), luminal B (HER2-) (19.2%), triple negative (9.9%), luminal B (HER2 +) (8.5%), and HER2-enriched (4.4%). There were 286 breast cancer deaths in total within three years. KM estimates showed women with HER2-enriched tumours had the worst survival at ages 50 to 69, while those with triple-negative tumours had the worst survival at ages 70 to 84. Adjusted HRs (95% confidence intervals) for mortality over 3 years compared to luminal A were 2.04 (1.43, 2.90) for luminal B (HER2-), 5.68 (3.40, 9.50) for triple negative, 2.22 (1.46, 3.38) for luminal B (HER2 +), and 2.93 (1.63, 5.27) for HER2-enriched. The imputed cohort adjusted HRs were attenuated, particularly for HER2-enriched (HR = 1.71 (1.01, 2.89)) and triple negative (HR = 2.74 (1.72, 4.37)). Like the general population, triple negative and HER2-enriched tumors had worse prognosis compared to luminal A tumors and their association with breast cancer mortality are similar in women with type 2 diabetes and the general population. However, our findings revealed differences in the survival ranking of HER2-enriched and triple-negative subtypes for breast cancer diagnosed in the 50-69 age group between women with type 2 diabetes and the general population, warranting further exploration.
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