Abstract
Introduction
Novel glucagon-like peptide-1 (GLP-1) receptor agonist oral semaglutide has demonstrated greater improvements in glycated hemoglobin (HbA1c) and body weight versus oral medications empagliflozin and sitagliptin, and injectable GLP-1 analog liraglutide, in the PIONEER clinical trial program. Based on these data, the present analysis aimed to evaluate the long-term cost-effectiveness of oral semaglutide versus empagliflozin, sitagliptin and liraglutide in Spain.
Methods
Outcomes were projected over patients’ lifetimes using the IQVIA CORE Diabetes Model (v9.0), discounted at 3.0% annually. Cohort characteristics and treatment effects were sourced from PIONEER 2 and 4 for the comparisons of oral semaglutide 14 mg versus empagliflozin 25 mg and liraglutide 1.8 mg, respectively, and PIONEER 3 for oral semaglutide 7 and 14 mg versus sitagliptin 100 mg. Costs were accounted from a healthcare payer perspective in 2020 euros (EUR). Patients were assumed to receive initial therapies until HbA1c exceeded 7.5% and then treatment-intensified to basal insulin.
Results
Oral semaglutide 14 mg was associated with improvements in quality-adjusted life expectancy of 0.13, 0.19 and 0.06 quality-adjusted life years (QALYs) versus empagliflozin 25 mg, sitagliptin 100 mg and liraglutide 1.8 mg, respectively, with direct costs EUR 168 higher versus empagliflozin and EUR 236 and 1415 lower versus sitagliptin and liraglutide, respectively. Oral semaglutide 14 mg was associated with an incremental cost-effectiveness ratio (ICER) of EUR 1339 per QALY gained versus empagliflozin and was considered dominant (clinically superior and cost saving) versus sitagliptin and liraglutide. Additional analyses demonstrated that oral semaglutide 7 mg was associated with improvements of 0.11 QALYs and increased costs of EUR 226 versus sitagliptin and was therefore associated with an ICER of EUR 2011 per QALY gained.
Conclusion
Oral semaglutide 14 mg was dominant versus sitagliptin and liraglutide, and cost-effective versus empagliflozin, for the treatment of type 2 diabetes in Spain.
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Acknowledgements
Funding
The study and the Rapid Service Fee was supported by funding from Novo Nordisk A/S, which provided consulting fees to Ossian Health Economics and Communications, Basel, Switzerland.
Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Author Contributions
The study was conceived and designed by all authors and conducted by Samuel Malkin. Samuel Malkin drafted the manuscript, which was reviewed, revised and approved by all authors.
Disclosures
Josep Vidal has the following financial relationships: advisor on scientific boards for Novo Nordisk and lectures for Eli Lilly and Company, Merck Sharp & Dohme and Novo Nordisk. Samuel Malkin and Barnaby Hunt are employees of Ossian Health Economics and Communications GmbH. Ossian received consulting fees from Novo Nordisk A/S to support preparation of the analysis. Virginia Martín and María Gallego Estébanez are employees of Novo Nordisk Pharma SA. Josep Franch-Nadal has received advisory and or speaking fees from AstraZeneca, Ascensia, Boehringer Ingelheim, GSK, Lilly, MSD, Novartis, Novo Nordisk, and Sanofi; he has received research grants to the institution from AstraZeneca, GSK, Lilly, MSD, Novartis, Sanofi, Boehringer Ingelheim and Novo Nordisk.
Compliance with Ethics Guidelines
This article is based on previously conducted clinical trials and does not contain any studies with human participants or animals performed by any of the authors.
Data Availability
The datasets generated during and or analyzed during the current study are available from the corresponding author on reasonable request.
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Franch-Nadal, J., Malkin, S.J.P., Hunt, B. et al. The Cost-Effectiveness of Oral Semaglutide in Spain: A Long-Term Health Economic Analysis Based on the PIONEER Clinical Trials. Adv Ther 39, 3180–3198 (2022). https://doi.org/10.1007/s12325-022-02156-8
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DOI: https://doi.org/10.1007/s12325-022-02156-8