Strategy and Research Department, National Health Insurance, Paris, Ile de France, France.
Diabetes Care. 2013 Feb;36(2):294-301. doi: 10.2337/dc12-0506. Epub 2012 Sep 10.
To explore in France the relationship between insulin glargine use and overall and specific cancer risks in type 2 diabetic patients compared with other basal insulins.
Data were extracted from French health insurance information system (Système National d'Information Inter-Régimes de l'Assurance Maladie) linked with data from the French Hospital Discharge database (Programme de Médicalisation des Systèmes d'Information). Included were 70,027 patients aged 40-79 years who started a basal insulin in 2007-2009. Cox proportional hazards models with age as time-scale were used to calculate multivariate-adjusted hazard ratios for associations between type of basal insulin and risk of overall cancer, breast cancer, and seven other cancer sites.
The median follow-up was 2.67 years in patients exposed to insulin glargine. Absolute event rates for all cancer in patients exposed to glargine versus other basal insulin users were 1,622 and 1,643 per 100,000 person-years, respectively. No significant association was observed between glargine exposure and overall cancer incidence after adjustment for sex, with a hazard ratio of 0.97 (95% CI 0.87-1.07), or after additional adjustment for any other hypoglycemic agent use and duration of diabetes. No increased risk of breast cancer was observed for glargine users compared with other basal insulins users, with a fully adjusted hazard ratio of 1.08 (0.72-1.62).
In a large cohort of patients newly treated by basal insulin, no increased risk of any cancer was observed in insulin glargine users compared with other basal insulin users. Because follow-up did not exceed 4 years, longer-term studies are needed.
在法国探索 2 型糖尿病患者使用甘精胰岛素与其他基础胰岛素相比,整体和特定癌症风险之间的关系。
数据从法国健康保险信息系统(Système National d'Information Inter-Régimes de l'Assurance Maladie)中提取,并与法国医院出院数据库(Programme de Médicalisation des Systèmes d'Information)中的数据相链接。纳入了 70027 名年龄在 40-79 岁之间的患者,他们在 2007-2009 年开始使用基础胰岛素。使用年龄作为时间尺度的 Cox 比例风险模型来计算基础胰岛素类型与整体癌症、乳腺癌和其他七个癌症部位风险之间的多变量调整后的风险比。
接受甘精胰岛素治疗的患者中位随访时间为 2.67 年。接受甘精胰岛素治疗的患者与其他基础胰岛素使用者相比,所有癌症的绝对事件发生率分别为每 100000 人年 1622 例和 1643 例。调整性别后,甘精胰岛素暴露与整体癌症发生率之间没有显著关联,风险比为 0.97(95%CI 0.87-1.07),或在进一步调整任何其他降血糖药物使用和糖尿病持续时间后也是如此。与其他基础胰岛素使用者相比,甘精胰岛素使用者乳腺癌风险没有增加,完全调整后的风险比为 1.08(0.72-1.62)。
在一项新接受基础胰岛素治疗的大型患者队列中,与其他基础胰岛素使用者相比,甘精胰岛素使用者的任何癌症风险均未增加。由于随访时间未超过 4 年,需要进行更长期的研究。