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Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis
BACKGROUND: Determining the relative cost-effectiveness between advanced therapeutic options for ulcerative colitis (UC) may optimize resource utilization. We evaluated total cost per response, cost per remission, and cost of safety events for patients with moderately-to-severely active UC after 52 ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724317/ https://www.ncbi.nlm.nih.gov/pubmed/36474165 http://dx.doi.org/10.1186/s12876-022-02590-6 |
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author | Jairath, Vipul Cohen, Russell D. Loftus, Edward V. Candela, Ninfa Lasch, Karen Schultz, Bob G. |
author_facet | Jairath, Vipul Cohen, Russell D. Loftus, Edward V. Candela, Ninfa Lasch, Karen Schultz, Bob G. |
author_sort | Jairath, Vipul |
collection | PubMed |
description | BACKGROUND: Determining the relative cost-effectiveness between advanced therapeutic options for ulcerative colitis (UC) may optimize resource utilization. We evaluated total cost per response, cost per remission, and cost of safety events for patients with moderately-to-severely active UC after 52 weeks of treatment with advanced therapies at standard dosing. METHODS: An analytic model was developed to estimate costs from the US healthcare system perspective associated with achieving efficacy outcomes and managing safety outcomes for advanced therapies approved for the treatment of UC. Numbers needed to treat (NNT) for response and remission, and numbers needed to harm (NNH) for serious adverse events (SAEs) and serious infections (SIs) were derived from a network meta-analysis of pivotal trials. NNT for induction and maintenance were combined with drug regimen costs to calculate cost per clinical remission. Cost of managing AEs was calculated using NNH for safety outcomes and published costs of treating respective AEs. RESULTS: Costs per remission were $205,240, $249,417, $267,463, $365,050, $579,622, $750,200, and $787,998 for tofacitinib 10 mg, tofacitinib 5 mg, infliximab, vedolizumab, golimumab, adalimumab, and ustekinumab, respectively. Incremental costs of SAEs and SIs collectively were $136,390, $90,333, $31,888, $31,061, $20,049, $12,059, and $0 for tofacitinib 5 mg, golimumab, adalimumab, tofacitinib 10 mg, infliximab, ustekinumab, and vedolizumab (reference), respectively. CONCLUSIONS: Tofacitinib was associated with the lowest cost per response and cost per remission, while vedolizumab had the lowest costs related to SAEs and SIs. Balancing efficacy versus safety is important when evaluating the costs associated with treatment of moderate-to-severe UC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02590-6. |
format | Online Article Text |
id | pubmed-9724317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97243172022-12-07 Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis Jairath, Vipul Cohen, Russell D. Loftus, Edward V. Candela, Ninfa Lasch, Karen Schultz, Bob G. BMC Gastroenterol Research Article BACKGROUND: Determining the relative cost-effectiveness between advanced therapeutic options for ulcerative colitis (UC) may optimize resource utilization. We evaluated total cost per response, cost per remission, and cost of safety events for patients with moderately-to-severely active UC after 52 weeks of treatment with advanced therapies at standard dosing. METHODS: An analytic model was developed to estimate costs from the US healthcare system perspective associated with achieving efficacy outcomes and managing safety outcomes for advanced therapies approved for the treatment of UC. Numbers needed to treat (NNT) for response and remission, and numbers needed to harm (NNH) for serious adverse events (SAEs) and serious infections (SIs) were derived from a network meta-analysis of pivotal trials. NNT for induction and maintenance were combined with drug regimen costs to calculate cost per clinical remission. Cost of managing AEs was calculated using NNH for safety outcomes and published costs of treating respective AEs. RESULTS: Costs per remission were $205,240, $249,417, $267,463, $365,050, $579,622, $750,200, and $787,998 for tofacitinib 10 mg, tofacitinib 5 mg, infliximab, vedolizumab, golimumab, adalimumab, and ustekinumab, respectively. Incremental costs of SAEs and SIs collectively were $136,390, $90,333, $31,888, $31,061, $20,049, $12,059, and $0 for tofacitinib 5 mg, golimumab, adalimumab, tofacitinib 10 mg, infliximab, ustekinumab, and vedolizumab (reference), respectively. CONCLUSIONS: Tofacitinib was associated with the lowest cost per response and cost per remission, while vedolizumab had the lowest costs related to SAEs and SIs. Balancing efficacy versus safety is important when evaluating the costs associated with treatment of moderate-to-severe UC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02590-6. BioMed Central 2022-12-06 /pmc/articles/PMC9724317/ /pubmed/36474165 http://dx.doi.org/10.1186/s12876-022-02590-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Jairath, Vipul Cohen, Russell D. Loftus, Edward V. Candela, Ninfa Lasch, Karen Schultz, Bob G. Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title | Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title_full | Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title_fullStr | Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title_full_unstemmed | Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title_short | Evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
title_sort | evaluating cost per remission and cost of serious adverse events of advanced therapies for ulcerative colitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9724317/ https://www.ncbi.nlm.nih.gov/pubmed/36474165 http://dx.doi.org/10.1186/s12876-022-02590-6 |
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