Diabetes Therapy | 2019

Oral Semaglutide Versus Empagliflozin, Sitagliptin and Liraglutide in the UK: Long-Term Cost-Effectiveness Analyses Based on the PIONEER Clinical Trial Programme

 
 
 
 
 
 
 
 

Abstract


Introduction The PIONEER trial programme showed that, after 52\xa0weeks, the novel oral glucagon-like peptide-1 (GLP-1) analogue semaglutide 14\xa0mg was associated with significantly greater reductions in glycated haemoglobin (HbA1c) versus a sodium-glucose cotransporter-2 inhibitor (empagliflozin 25\xa0mg), a dipeptidyl peptidase-4 inhibitor (sitagliptin 100\xa0mg) and an injectable GLP-1 analogue (liraglutide 1.8\xa0mg). The aim of the present analysis was to assess the long-term cost-effectiveness of oral semaglutide 14\xa0mg versus each of these comparators in the UK setting. Methods Analyses were performed from a healthcare payer perspective using the IQVIA CORE Diabetes Model, in which outcomes were projected over patient lifetimes (50\xa0years). Baseline cohort characteristics and treatment effects were based on 52-week data from the PIONEER 2, 3 and 4 randomised controlled trials, comparing oral semaglutide with empagliflozin, sitagliptin and liraglutide, respectively. Treatment switching occurred when HbA1c exceeded 7.5% (58\xa0mmol/mol). Utilities, treatment costs and costs of diabetes-related complications (in pounds sterling [GBP]) were taken from published sources. The acquisition cost of oral semaglutide was assumed to match that of once-weekly semaglutide. Results Oral semaglutide was associated with improvements in quality-adjusted life expectancy of 0.09 quality-adjusted life years (QALYs) versus empagliflozin, 0.20 QALYs versus sitagliptin and 0.07 QALYs versus liraglutide. Direct costs over a patient’s lifetime were GBP 971 and GBP 963 higher with oral semaglutide than with empagliflozin and sitagliptin, respectively, but GBP 1551 lower versus liraglutide. Oral semaglutide was associated with a reduced incidence of diabetes-related complications versus all comparators. Therefore, oral semaglutide 14\xa0mg was associated with incremental cost-effectiveness ratios of GBP 11,006 and 4930 per QALY gained versus empagliflozin 25\xa0mg and sitagliptin 100\xa0mg, respectively, and was more effective and less costly (dominant) versus liraglutide 1.8\xa0mg. Conclusion Oral semaglutide was cost-effective versus empagliflozin and sitagliptin, and dominant versus liraglutide, for the treatment of type 2 diabetes in the UK.

Volume 11
Pages 259 - 277
DOI 10.1007/s13300-019-00736-6
Language English
Journal Diabetes Therapy

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