Ericsson Åsa, Glah Divina, Lorenzi Maria, Jansen Jeroen P, Fridhammar Adam
Diabetes Marketing, Novo Nordisk Scandinavia AB, Malmö, Sweden.
Formerly: Health Economics & Outcomes Research, Novo Nordisk Ltd, Gatwick, United Kingdom.
PLoS One. 2018 Feb 6;13(2):e0191953. doi: 10.1371/journal.pone.0191953. eCollection 2018.
We assessed the cost-effectiveness of the glucagon-like peptide 1 receptor agonists liraglutide 1.8 mg and lixisenatide 20 μg (both added to basal insulin) in patients with type 2 diabetes (T2D) in Sweden.
The Swedish Institute for Health Economics cohort model for T2D was used to compare liraglutide and lixisenatide (both added to basal insulin), with a societal perspective and with comparative treatment effects derived by indirect treatment comparison (ITC). Drug prices were 2016 values, and all other costs 2015 values. The cost-effectiveness of IDegLira (fixed-ratio combination of insulin degludec and liraglutide) versus lixisenatide plus basal insulin was also assessed, under different sets of assumptions.
From the ITC, decreases in HbA1c were -1.32% and -0.43% with liraglutide and lixisenatide, respectively; decreases in BMI were -1.29 and -0.65 kg/m2, respectively. An estimated 2348 cases of retinopathy, 265 of neuropathy and 991 of nephropathy would be avoided with liraglutide compared with lixisenatide in a cohort of 10,000 patients aged over 40 years. In the base-case analysis, total direct costs were higher with liraglutide than lixisenatide, but costs associated with complications were lower. The cost/quality-adjusted life-year (QALY) for liraglutide added to basal insulin was SEK30,802. Base-case findings were robust in sensitivity analyses, except when glycated haemoglobin (HbA1c) differences for liraglutide added to basal insulin were abolished, suggesting these benefits were driving the cost/QALY. With liraglutide 1.2 mg instead of liraglutide 1.8 mg (adjusted for efficacy and cost), liraglutide added to basal insulin was dominant over lixisenatide 20μg.IDegLira was dominant versus lixisenatide plus basal insulin when a defined daily dose was used in the model.
The costs/QALY for liraglutide, 1.8 or 1.2 mg, added to basal insulin, and for IDegLira (all compared with lixisenatide 20 μg added to basal insulin) were below the threshold considered low by Swedish authorities. In some scenarios, liraglutide and IDegLira were cost-saving.
我们评估了胰高血糖素样肽-1受体激动剂利拉鲁肽1.8毫克和利司那肽20微克(均添加到基础胰岛素中)在瑞典2型糖尿病(T2D)患者中的成本效益。
采用瑞典卫生经济研究所的2型糖尿病队列模型,从社会角度比较利拉鲁肽和利司那肽(均添加到基础胰岛素中),并通过间接治疗比较(ITC)得出比较治疗效果。药品价格为2016年的数值,所有其他成本为2015年的数值。还在不同假设组下评估了德谷胰岛素利拉鲁肽(德谷胰岛素和利拉鲁肽的固定比例组合)与利司那肽加基础胰岛素相比的成本效益。
通过ITC,利拉鲁肽和利司那肽使糖化血红蛋白(HbA1c)分别降低了-1.32%和-0.43%;体重指数(BMI)分别降低了-1.29和-0.65kg/m²。在10000名40岁以上患者的队列中,与利司那肽相比,使用利拉鲁肽估计可避免2348例视网膜病变、265例神经病变和991例肾病。在基础病例分析中,利拉鲁肽的总直接成本高于利司那肽,但与并发症相关的成本较低。添加到基础胰岛素中的利拉鲁肽的成本/质量调整生命年(QALY)为30802瑞典克朗。除了基础胰岛素中添加利拉鲁肽的糖化血红蛋白(HbA1c)差异被消除的情况外,基础病例研究结果在敏感性分析中是稳健的,这表明这些益处推动了成本/QALY。用1.2毫克利拉鲁肽代替1.8毫克利拉鲁肽(根据疗效和成本进行调整),添加到基础胰岛素中的利拉鲁肽优于20微克利司那肽。当在模型中使用限定日剂量时,德谷胰岛素利拉鲁肽优于利司那肽加基础胰岛素。
添加到基础胰岛素中的1.8毫克或1.2毫克利拉鲁肽以及德谷胰岛素利拉鲁肽(均与添加到基础胰岛素中的20微克利司那肽相比)的成本/QALY低于瑞典当局认为较低的阈值。在某些情况下,利拉鲁肽和德谷胰岛素利拉鲁肽具有成本节约效果。