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Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK
OBJECTIVE: To determine the cost effectiveness of secukinumab, a fully human interleukin-17A inhibitor, for adults in the UK with active ankylosing spondylitis (AS) who have not responded adequately to previous treatment with conventional care (CC; biologic-naïve population) or previous biologic the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021464/ https://www.ncbi.nlm.nih.gov/pubmed/29797186 http://dx.doi.org/10.1007/s40273-018-0675-9 |
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author | Emery, Paul Van Keep, Marjolijn Beard, Steve Graham, Chris Miles, LaStella Jugl, Steffen Marc Gunda, Praveen Halliday, Anna Marzo-Ortega, Helena |
author_facet | Emery, Paul Van Keep, Marjolijn Beard, Steve Graham, Chris Miles, LaStella Jugl, Steffen Marc Gunda, Praveen Halliday, Anna Marzo-Ortega, Helena |
author_sort | Emery, Paul |
collection | PubMed |
description | OBJECTIVE: To determine the cost effectiveness of secukinumab, a fully human interleukin-17A inhibitor, for adults in the UK with active ankylosing spondylitis (AS) who have not responded adequately to previous treatment with conventional care (CC; biologic-naïve population) or previous biologic therapy (biologic-experienced population). PERSPECTIVE AND SETTING: UK National Health Service (NHS). METHODS: The model was structured as a 3-month decision tree leading into a Markov model. Comparators were licensed tumour necrosis factor inhibitors (including available biosimilars) and CC in the biologic-naïve and biologic-experienced populations, respectively. Clinical parameters captured treatment response, short-term disease activity and patient functioning, as well as long-term structural disease progression. Utilities were derived from secukinumab trial data. List prices were used for all drugs. The cost year was 2017 and costs and outcomes were discounted at 3.5%. RESULTS: In the biologic-naïve population, secukinumab dominated adalimumab and certolizumab pegol. Incremental cost-effectiveness ratios (ICERs) versus other comparators were either below £10,000 per quality-adjusted life-year (QALY) gained or south-west ICERs that implied cost effectiveness of secukinumab. In biologic-experienced patients, the ICER for secukinumab versus CC was £4927 per QALY gained. Treatment response rates, short-term treatment effects, long-term radiographic progression and biologic acquisition costs were key model drivers. Scenario analysis found results to be robust to changes in model structural assumptions. Probabilistic analysis identified greater uncertainty in results in the biologic-naïve population. CONCLUSIONS: Even at list price, secukinumab appears to represent a cost-effective use of NHS resources for biologic-naïve and biologic-experienced patients with active AS. Further research on long-term radiographic progression outcomes would be valuable for future cost-effectiveness analyses in AS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40273-018-0675-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6021464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-60214642018-07-06 Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK Emery, Paul Van Keep, Marjolijn Beard, Steve Graham, Chris Miles, LaStella Jugl, Steffen Marc Gunda, Praveen Halliday, Anna Marzo-Ortega, Helena Pharmacoeconomics Original Research Article OBJECTIVE: To determine the cost effectiveness of secukinumab, a fully human interleukin-17A inhibitor, for adults in the UK with active ankylosing spondylitis (AS) who have not responded adequately to previous treatment with conventional care (CC; biologic-naïve population) or previous biologic therapy (biologic-experienced population). PERSPECTIVE AND SETTING: UK National Health Service (NHS). METHODS: The model was structured as a 3-month decision tree leading into a Markov model. Comparators were licensed tumour necrosis factor inhibitors (including available biosimilars) and CC in the biologic-naïve and biologic-experienced populations, respectively. Clinical parameters captured treatment response, short-term disease activity and patient functioning, as well as long-term structural disease progression. Utilities were derived from secukinumab trial data. List prices were used for all drugs. The cost year was 2017 and costs and outcomes were discounted at 3.5%. RESULTS: In the biologic-naïve population, secukinumab dominated adalimumab and certolizumab pegol. Incremental cost-effectiveness ratios (ICERs) versus other comparators were either below £10,000 per quality-adjusted life-year (QALY) gained or south-west ICERs that implied cost effectiveness of secukinumab. In biologic-experienced patients, the ICER for secukinumab versus CC was £4927 per QALY gained. Treatment response rates, short-term treatment effects, long-term radiographic progression and biologic acquisition costs were key model drivers. Scenario analysis found results to be robust to changes in model structural assumptions. Probabilistic analysis identified greater uncertainty in results in the biologic-naïve population. CONCLUSIONS: Even at list price, secukinumab appears to represent a cost-effective use of NHS resources for biologic-naïve and biologic-experienced patients with active AS. Further research on long-term radiographic progression outcomes would be valuable for future cost-effectiveness analyses in AS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s40273-018-0675-9) contains supplementary material, which is available to authorized users. Springer International Publishing 2018-05-25 2018 /pmc/articles/PMC6021464/ /pubmed/29797186 http://dx.doi.org/10.1007/s40273-018-0675-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Article Emery, Paul Van Keep, Marjolijn Beard, Steve Graham, Chris Miles, LaStella Jugl, Steffen Marc Gunda, Praveen Halliday, Anna Marzo-Ortega, Helena Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title | Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title_full | Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title_fullStr | Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title_full_unstemmed | Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title_short | Cost Effectiveness of Secukinumab for the Treatment of Active Ankylosing Spondylitis in the UK |
title_sort | cost effectiveness of secukinumab for the treatment of active ankylosing spondylitis in the uk |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6021464/ https://www.ncbi.nlm.nih.gov/pubmed/29797186 http://dx.doi.org/10.1007/s40273-018-0675-9 |
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