Key result
Adding an SGLT2 inhibitor saves ~$9,500 and improves lifetime survival versus switching to a GLP-1 RA.
Why the study?
The lifetime cost-effectiveness of adding SGLT2 inhibitors versus switching to GLP-1 RAs in type 2 diabetes patients not at HbA1c target after metformin and DPP-4 inhibitor dual therapy was unclear.
Does adding SGLT2 inhibitors improve cost-effectiveness and outcomes compared to switching to GLP-1 RAs in patients with type 2 diabetes not at target on metformin and DPP-4 inhibitors?
Does adding SGLT2 inhibitors improve cost-effectiveness and outcomes compared to switching to GLP-1 RAs in patients with type 2 diabetes not at target on metformin and DPP-4 inhibitors?
Effect estimate: 0.049 LYs gained, 0.026 QALYs gained, $9511 saved
In a US payer simulation, adding an SGLT2 inhibitor to metformin and a DPP-4 inhibitor was more effective and less costly than switching to a GLP-1 RA for patients with type 2 diabetes not at glycemic target.
May support adding SGLT2 inhibitors for modeled cost savings in T2D; leaves open prospective validation before practice change.
OBJECTIVES: Using a US payer perspective, this study aimed to compare the lifetime cost-effectiveness of adding sodium-glucose cotransporter 2 (SGLT2) inhibitors vs switching to glucagon-like peptide 1 receptor agonists (GLP-1 RAs) among patients with type 2 diabetes who were not at glycated hemoglobin A1c target after dual therapy with metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors. STUDY DESIGN: The cost-effectiveness analysis was performed with the validated IQVIA Core Diabetes Model. Treatment effects were obtained from randomized clinical trials with economic data based on published literature. METHODS: Risk of treatment-emergent adverse events and complications were simulated using submodels informed by published risk equations adjusted for patient characteristics, physiological parameters, and history of complications. Outcomes included cumulative incidence of micro- and macrovascular complications, life-years (LYs), quality-adjusted life-years (QALYs), and total costs. Scenario analyses were performed to assess robustness of results to variations in clinical and cost inputs and assumptions. RESULTS: Over a lifetime time horizon, adding an SGLT2 inhibitor dominated the strategy of switching to a GLP-1 RA, improving survival by 0.049 LYs and 0.026 QALYs, and was associated with cost savings of $9511. The majority of the scenario analyses confirmed dominance of the DPP-4 inhibitor + SGLT2 inhibitor pathway vs the GLP-1 RA pathway. The probabilistic sensitivity analysis reinforced the base-case finding of cost savings while gaining QALYs. CONCLUSIONS: Intensification with an SGLT2 inhibitor on top of a DPP-4 inhibitor demonstrated slightly better efficacy and cost savings compared with switching to a GLP-1 RA in patients not at glycemic goal with metformin and a DPP-4 inhibitor.
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PhD S. Pinar Bilir Manjiri Pawaskar (2021) studied type 2 diabetes. SGLT2 inhibitors vs. Switching to GLP-1 receptor agonists was evaluated on Life-years (LYs), quality-adjusted life-years (QALYs), and total costs (0.049 LYs gained, 0.026 QALYs gained, $9511 saved). Adding an SGLT2 inhibitor dominated switching to a GLP-1 RA over a lifetime horizon, improving survival by 0.049 life-years and 0.026 QALYs while saving $9,511.
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