Aranishi Toshihiko, Igarashi Ataru, Hara Kazuo, Osumili Beatrice, Cai Zhihong, Mizogaki Aska, Sato Manaka, Takeuchi Masakazu, Minghetti Alice, Hunt Barnaby, Kadowaki Takashi
Eli Lilly Japan K.K., 5-1-28 Isogami-dori, Chuo-Ku, Kobe, Japan.
Department of Health Policy and Public Health, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 13-0033, Japan.
Diabetes Ther. 2025 Mar;16(3):431-445. doi: 10.1007/s13300-024-01675-7. Epub 2024 Dec 21.
This analysis aimed to evaluate the long-term cost-effectiveness of tirzepatide 5 mg versus dulaglutide 0.75 mg (both administered once weekly) in people not achieving glycemic control on metformin, based on the results of the head-to-head SURPASS J-mono trial from a Japanese healthcare payer perspective.
A cost-utility analysis was performed over a 50-year time horizon using an implementation of the UKPDS Outcomes Model 2 developed in Microsoft Excel. Baseline cohort characteristics, treatment effects and adverse event rates were sourced from the SURPASS J-mono trial. Simulated patients were assumed to receive either tirzepatide 5 mg or dulaglutide 0.75 mg until HbA1c exceeded 8.0%, at which point treatment was discontinued and basal insulin was initiated. Direct costs were derived from the Japan Medical Data Center claims database. Future costs and clinical benefits were discounted at 2% annually.
In this cost-utility modeling analysis, tirzepatide 5 mg was associated with lower diabetes-related complication rates, improved life expectancy, improved quality-adjusted life expectancy and higher direct costs versus dulaglutide 0.75 mg. This resulted in an incremental cost-effectiveness ratio (ICER) of JPY (Japanese yen) 1,302,240 per quality-adjusted life year (QALY) gained for tirzepatide 5 mg versus dulaglutide 0.75 mg (JPY 140 = USD 1). Tirzepatide remained cost-effective versus dulaglutide over a range of sensitivity analyses.
In this analysis, tirzepatide 5 mg was associated with an ICER below the commonly quoted willingness-to-pay threshold of JPY 5,000,000 per QALY gained, suggesting that tirzepatide is a cost-effective treatment option for adult patients with type 2 diabetes mellitus, compared with dulaglutide 0.75 mg.
本分析旨在基于日本医疗保健支付方的视角,根据头对头的SURPASS J-单药试验结果,评估替尔泊肽5毫克与度拉糖肽0.75毫克(均每周给药一次)在使用二甲双胍未实现血糖控制的人群中的长期成本效益。
使用在Microsoft Excel中开发的UKPDS结果模型2的一个版本,在50年的时间范围内进行成本效用分析。基线队列特征、治疗效果和不良事件发生率均来自SURPASS J-单药试验。假设模拟患者接受替尔泊肽5毫克或度拉糖肽0.75毫克治疗,直至糖化血红蛋白超过8.0%,此时停止治疗并开始使用基础胰岛素。直接成本来自日本医疗数据中心的索赔数据库。未来成本和临床效益按每年2%进行贴现。
在这项成本效用模型分析中,与度拉糖肽0.75毫克相比,替尔泊肽5毫克与较低的糖尿病相关并发症发生率、更长的预期寿命、更高的质量调整预期寿命以及更高的直接成本相关。这导致替尔泊肽5毫克相对于度拉糖肽0.75毫克每获得一个质量调整生命年(QALY)的增量成本效益比(ICER)为1,302,240日元(140日元 = 1美元)。在一系列敏感性分析中,替尔泊肽与度拉糖肽相比仍具有成本效益。
在本分析中,替尔泊肽5毫克的ICER低于通常引用的每获得一个QALY支付意愿阈值5,000,000日元,这表明与度拉糖肽0.75毫克相比,替尔泊肽是成年2型糖尿病患者具有成本效益的治疗选择。