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Cost-effectiveness of empagliflozin in patients with type 2 diabetes and established cardiovascular disease in China.
Ramos, Mafalda; Men, Peng; Wang, Xu; Ustyugova, Anastasia; Lamotte, Mark.
Afiliación
  • Ramos M; IQVIA Global HEOR, Lagoas Park, Edifício 3 - Piso 3, 2740-266, Porto Salvo, Portugal. Mafalda.ramos@iqvia.com.
  • Men P; Department of Pharmacy, Peking University Third Hospital, Beijing, 100191, China.
  • Wang X; Institute for Drug Evaluation, Peking University Health Science Center, Beijing, 100191, China.
  • Ustyugova A; Boehringer Ingelheim, Beijing, China.
  • Lamotte M; Boehringer Ingelheim, Ingelheim Am Rhein, Germany.
Cost Eff Resour Alloc ; 19(1): 46, 2021 Aug 04.
Article en En | MEDLINE | ID: mdl-34348729
ABSTRACT

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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Health_economic_evaluation / Prognostic_studies Aspecto: Patient_preference Idioma: En Revista: Cost Eff Resour Alloc Año: 2021 Tipo del documento: Article País de afiliación: Portugal

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Health_economic_evaluation / Prognostic_studies Aspecto: Patient_preference Idioma: En Revista: Cost Eff Resour Alloc Año: 2021 Tipo del documento: Article País de afiliación: Portugal