Borthwick Diabetes Research Centre, Lister Hospital (East and North Hertfordshire NHS Trust), Stevenage, UK.
Novo Nordisk Ltd, Gatwick, UK.
Diabetes Obes Metab. 2019 Mar;21(3):611-621. doi: 10.1111/dom.13564. Epub 2018 Nov 28.
Glucagon-like peptide-1 (GLP-1) receptor agonists are appealing as glucose-lowering therapy for individuals with type 2 diabetes mellitus (T2DM) as they also reduce body weight and are associated with low rates of hypoglycaemia. This analysis assessed the long-term cost-effectiveness of semaglutide 0.5 and 1 mg vs dulaglutide 1.5 mg (two once-weekly GLP-1 receptor agonists) from a UK healthcare payer perspective, based on the head-to-head SUSTAIN 7 trial, to inform healthcare decision making.
Long-term outcomes were projected using the IQVIA CORE Diabetes Model (version 9.0). Baseline cohort characteristics, changes in physiological parameters and adverse event rates were derived from the 40-week SUSTAIN 7 trial. Costs to a healthcare payer were assessed, and these captured pharmacy costs and costs of complications. Utilities were taken from published sources.
Once-weekly semaglutide 0.5 and 1 mg were associated with improvements in quality-adjusted life expectancy of 0.04 and 0.10 quality-adjusted life years, respectively, compared with dulaglutide 1.5 mg. Clinical benefits were achieved at reduced costs, with lifetime cost savings of GBP 35 with once-weekly semaglutide 0.5 mg and GBP 106 with the once-weekly semaglutide 1 mg, resulting from fewer diabetes-related complications due to better glycaemic control. Therefore, both doses of once-weekly semaglutide were considered dominant vs dulaglutide 1.5 mg (improving outcomes and reducing costs).
Compared with treatment with dulaglutide, once-weekly semaglutide represents a cost-effective option for treating individuals in the UK with T2DM who are not achieving glycaemic control with metformin, projected to both improve clinical outcomes and reduce costs.
胰高血糖素样肽-1(GLP-1)受体激动剂作为 2 型糖尿病(T2DM)患者的降糖治疗药物具有吸引力,因为它们还可以减轻体重,并且低血糖发生率低。本分析从英国医疗保健支付者的角度评估了每周一次的司美格鲁肽 0.5mg 和 1mg 与每周一次的度拉鲁肽 1.5mg(两种 GLP-1 受体激动剂)在头对头的 SUSTAIN 7 试验中的长期成本效益,以为医疗保健决策提供信息。
使用 IQVIA CORE Diabetes Model(版本 9.0)预测长期结果。基线队列特征、生理参数变化和不良事件发生率源自 40 周的 SUSTAIN 7 试验。评估了医疗保健支付者的成本,这些成本包括药房成本和并发症成本。效用来自已发表的来源。
与每周一次的度拉鲁肽 1.5mg 相比,每周一次的司美格鲁肽 0.5mg 和 1mg 分别使质量调整预期寿命提高了 0.04 和 0.10 个质量调整生命年。临床获益以降低成本为代价实现,每周一次的司美格鲁肽 0.5mg 可节省 35 英镑,每周一次的司美格鲁肽 1mg 可节省 106 英镑,这是由于更好的血糖控制减少了糖尿病相关并发症,从而实现了终生成本节约。因此,每周一次的司美格鲁肽的两种剂量均被认为优于每周一次的度拉鲁肽 1.5mg(改善结果并降低成本)。
与度拉鲁肽治疗相比,每周一次的司美格鲁肽代表了一种具有成本效益的选择,可用于治疗英国 T2DM 患者,这些患者在服用二甲双胍时血糖控制不佳,预计可改善临床结局并降低成本。