Cost-effectiveness of empagliflozin in patients with type 2 diabetes and established cardiovascular disease in China

被引:8
|
作者
Ramos, Mafalda [1 ]
Men, Peng [2 ,3 ]
Wang, Xu [4 ]
Ustyugova, Anastasia [5 ]
Lamotte, Mark [6 ]
机构
[1] IQVIA Global HEOR, Lagoas Pk,Edificio 3 Piso, P-2740266 Porto Salvo, Portugal
[2] Peking Univ Third Hosp, Dept Pharm, Beijing 100191, Peoples R China
[3] Peking Univ, Hlth Sci Ctr, Inst Drug Evaluat, Beijing 100191, Peoples R China
[4] Boehringer Ingelheim GmbH & Co KG, Beijing, Peoples R China
[5] Boehringer Ingelheim GmbH & Co KG, Ingelheim, Germany
[6] IQVIA, Global HEOR, Zaventem, Belgium
关键词
Cost-effectiveness; Empagliflozin; Type; 2; diabetes; Cardiovascular outcomes; Core Diabetes Model; ACTIVE COMPARATOR; UTILITY VALUES; OUTCOMES; MELLITUS; SITAGLIPTIN; RISK; LIRAGLUTIDE; GLUCOSE; MODEL; PREVALENCE;
D O I
10.1186/s12962-021-00299-z
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background In several cardiovascular outcome trials (CVOTs), empagliflozin (SGLT-2 inhibitor), sitagliptin (DPP-4 inhibitor) and liraglutide (GLP-1 receptor agonist) + standard of care (SoC) were compared to SoC in patients with type 2 diabetes and established cardiovascular disease (CVD). This study assessed the cost-effectiveness (CE) of empagliflozin + SoC in comparison to sitagliptin + SoC and liraglutide + SoC based on the respective CVOT. Methods The IQVIA Core Diabetes Model (CDM) was calibrated to reproduce the CVOT outcomes. EMPA-REG OUTCOME baseline characteristics and CVOT specific treatment effects on risk factors for cardiovascular disease (HbA1c, BMI, blood pressure, lipids) were applied. Three-year observed cardiovascular events of empagliflozin + SoC versus sitagliptin + SoC and liraglutide + SoC were derived from EMPA-REG OUTCOME and an indirect treatment comparison. Relative risk adjustments to calibrate the CDM were obtained after a trial and error process to match as closely the observed and CDM-predicted outcomes. The drug-specific treatment effects were considered up until HbA1c reached 8.5% and treatment switch occurred. After this switch, the United Kingdom Prospective Diabetes Study 82 risk equations predicted events based on co-existing risk factors and treatment intensification to basal bolus insulin were applied. The analysis was conducted from the perspective of the Chinese healthcare system applying 3% discounting. The time horizon was lifelong. Results Empagliflozin + SoC provides additional Quality Adjusted Life years (QALY + 0.564) for an incremental cost of 42,497RMB (US$6053) compared to sitagliptin + SoC, resulting in an Incremental Cost Utility Ratio of 75,349RMB (US$10,732), thus below the willingness-to-pay threshold of 212,676RMB, corresponding to three times the Gross Domestic Product in China (2019). Compared to liraglutide + SoC, empagliflozin + SoC use leads to 0.211QALY gained and cost savings of 71,427RMB (US$10,173) and is as such dominant. Scenario and probabilistic sensitivity analyses demonstrated the robustness of the results. Conclusion Results suggest that empagliflozin + SoC is cost-effective compared to sitagliptin + SoC and liraglutide + SoC at a willingness-to-pay threshold of 212,676RMB ($30,292)/QALY.
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页数:11
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