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Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden
BACKGROUND: Human monoclonal antibody ustekinumab is a novel Crohn’s disease (CD) treatment blocking pro-inflammatory cytokines interleukin-12 and 23. The study’s objective was to assess cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effectiveness mode...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090969/ https://www.ncbi.nlm.nih.gov/pubmed/30123097 http://dx.doi.org/10.1186/s12962-018-0114-y |
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author | Hansson-Hedblom, Amanda Almond, Chrissy Borgström, Fredrik Sly, Indeg Enkusson, Dana Troelsgaard Buchholt, Anders Karlsson, Linda |
author_facet | Hansson-Hedblom, Amanda Almond, Chrissy Borgström, Fredrik Sly, Indeg Enkusson, Dana Troelsgaard Buchholt, Anders Karlsson, Linda |
author_sort | Hansson-Hedblom, Amanda |
collection | PubMed |
description | BACKGROUND: Human monoclonal antibody ustekinumab is a novel Crohn’s disease (CD) treatment blocking pro-inflammatory cytokines interleukin-12 and 23. The study’s objective was to assess cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effectiveness model with an induction phase decision-tree structure and a maintenance phase Markov cohort structure was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in patients who had failed conventional care, some of which had tried TNF-alpha-inhibitor(s) without experiencing treatment failure or side effects (“conventional care failure population”) and to vedolizumab in patients previously failing TNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase-III trials. Maintenance and comparator efficacy came from network-meta and treatment-sequence analyses. Resource use and unit costs were derived from literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and 2-year treatment duration. The results robustness was tested in univariate and probabilistic sensitivity analyses. Cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in conventional care failure population (costs: − €6984, QALYs: + 0.232). In TNF-alpha-inhibitor failure population ustekinumab accrued 0.133 more QALYs than vedolizumab, yielding a €30,282 incremental cost-effectiveness ratio. Results were sensitive to decreasing the time horizon and increased treatment duration. At Swedish reference willingness-to-pay of €63,000 (SEK 600,000), ustekinumab had 94% probability of being cost-effective versus adalimumab, and 72% versus vedolizumab. CONCLUSIONS: Results indicate ustekinumab dominates adalimumab in conventional care failure population, and is cost-effective versus vedolizumab in TNF-alpha-inhibitor failure population. |
format | Online Article Text |
id | pubmed-6090969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60909692018-08-17 Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden Hansson-Hedblom, Amanda Almond, Chrissy Borgström, Fredrik Sly, Indeg Enkusson, Dana Troelsgaard Buchholt, Anders Karlsson, Linda Cost Eff Resour Alloc Research BACKGROUND: Human monoclonal antibody ustekinumab is a novel Crohn’s disease (CD) treatment blocking pro-inflammatory cytokines interleukin-12 and 23. The study’s objective was to assess cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effectiveness model with an induction phase decision-tree structure and a maintenance phase Markov cohort structure was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in patients who had failed conventional care, some of which had tried TNF-alpha-inhibitor(s) without experiencing treatment failure or side effects (“conventional care failure population”) and to vedolizumab in patients previously failing TNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase-III trials. Maintenance and comparator efficacy came from network-meta and treatment-sequence analyses. Resource use and unit costs were derived from literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and 2-year treatment duration. The results robustness was tested in univariate and probabilistic sensitivity analyses. Cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in conventional care failure population (costs: − €6984, QALYs: + 0.232). In TNF-alpha-inhibitor failure population ustekinumab accrued 0.133 more QALYs than vedolizumab, yielding a €30,282 incremental cost-effectiveness ratio. Results were sensitive to decreasing the time horizon and increased treatment duration. At Swedish reference willingness-to-pay of €63,000 (SEK 600,000), ustekinumab had 94% probability of being cost-effective versus adalimumab, and 72% versus vedolizumab. CONCLUSIONS: Results indicate ustekinumab dominates adalimumab in conventional care failure population, and is cost-effective versus vedolizumab in TNF-alpha-inhibitor failure population. BioMed Central 2018-08-02 /pmc/articles/PMC6090969/ /pubmed/30123097 http://dx.doi.org/10.1186/s12962-018-0114-y Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hansson-Hedblom, Amanda Almond, Chrissy Borgström, Fredrik Sly, Indeg Enkusson, Dana Troelsgaard Buchholt, Anders Karlsson, Linda Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title | Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title_full | Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title_fullStr | Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title_full_unstemmed | Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title_short | Cost-effectiveness of ustekinumab in moderate to severe Crohn’s disease in Sweden |
title_sort | cost-effectiveness of ustekinumab in moderate to severe crohn’s disease in sweden |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090969/ https://www.ncbi.nlm.nih.gov/pubmed/30123097 http://dx.doi.org/10.1186/s12962-018-0114-y |
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