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Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis

OBJECTIVE: To evaluate cost-utility of infliximab and adalimumab for the treatment of moderate-to-severe ulcerative colitis (UC) refractory to conventional therapies in Canada. METHODS: A Markov model was constructed to evaluate incremental cost-utility ratios (ICUR) of 5 mg/kg and 10 mg/kg inflixim...

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Autores principales: Xie, Feng, Blackhouse, Gord, Assasi, Nazila, Gaebel, Kathryn, Robertson, Diana, Goeree, Ron
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797497/
https://www.ncbi.nlm.nih.gov/pubmed/20003364
http://dx.doi.org/10.1186/1478-7547-7-20
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author Xie, Feng
Blackhouse, Gord
Assasi, Nazila
Gaebel, Kathryn
Robertson, Diana
Goeree, Ron
author_facet Xie, Feng
Blackhouse, Gord
Assasi, Nazila
Gaebel, Kathryn
Robertson, Diana
Goeree, Ron
author_sort Xie, Feng
collection PubMed
description OBJECTIVE: To evaluate cost-utility of infliximab and adalimumab for the treatment of moderate-to-severe ulcerative colitis (UC) refractory to conventional therapies in Canada. METHODS: A Markov model was constructed to evaluate incremental cost-utility ratios (ICUR) of 5 mg/kg and 10 mg/kg infliximab and adalimumab therapies compared to 'usual care' in treating a hypothetical cohort of patients (aged 40 years and weighing 80 kg) over a five-year time horizon from the perspective of a publicly-funded health care system. Clinical parameters were derived from the Active Ulcerative Colitis Trials 1 and 2. Costs were obtained through provincial drug benefit plans. ICUR was the main outcome measure and both deterministic and probabilistic sensitivity analyses were conducted. RESULTS: Compared to the strategy A ('usual care') in the base case analysis, the ICURs were CA$358,088/QALY for the strategy B ('5 mg/kg infliximab + adalimumab') and CA$575,540/QALY for the strategy C ('5 mg/kg and 10 mg/kg infliximab + adalimumab'). The results were sensitive to: the remission rates maintained in responders to 'usual care' and to 5 mg/kg infliximab, the rate of remission induced by adalimumab in non-responders to 5 mg/kg infliximab, early surgery rate, and utility values. When the willingness to pay (WTP) was less than CA$150,000/QALY, the probability of 'usual care' being the optimal strategy was 1.0. The probability of strategy B being optimal was 0.5 when the WTP approximated CA$400,000/QALY. CONCLUSIONS: The ICURs of anti-TNF-α drugs were not satisfactory in treating patients with moderate-to-severe refractory UC. Future research could be aimed at the long-term clinical benefits of these drugs, especially adalimumab for patients intolerant or unresponsive to infliximab treatment.
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spelling pubmed-27974972009-12-24 Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis Xie, Feng Blackhouse, Gord Assasi, Nazila Gaebel, Kathryn Robertson, Diana Goeree, Ron Cost Eff Resour Alloc Research OBJECTIVE: To evaluate cost-utility of infliximab and adalimumab for the treatment of moderate-to-severe ulcerative colitis (UC) refractory to conventional therapies in Canada. METHODS: A Markov model was constructed to evaluate incremental cost-utility ratios (ICUR) of 5 mg/kg and 10 mg/kg infliximab and adalimumab therapies compared to 'usual care' in treating a hypothetical cohort of patients (aged 40 years and weighing 80 kg) over a five-year time horizon from the perspective of a publicly-funded health care system. Clinical parameters were derived from the Active Ulcerative Colitis Trials 1 and 2. Costs were obtained through provincial drug benefit plans. ICUR was the main outcome measure and both deterministic and probabilistic sensitivity analyses were conducted. RESULTS: Compared to the strategy A ('usual care') in the base case analysis, the ICURs were CA$358,088/QALY for the strategy B ('5 mg/kg infliximab + adalimumab') and CA$575,540/QALY for the strategy C ('5 mg/kg and 10 mg/kg infliximab + adalimumab'). The results were sensitive to: the remission rates maintained in responders to 'usual care' and to 5 mg/kg infliximab, the rate of remission induced by adalimumab in non-responders to 5 mg/kg infliximab, early surgery rate, and utility values. When the willingness to pay (WTP) was less than CA$150,000/QALY, the probability of 'usual care' being the optimal strategy was 1.0. The probability of strategy B being optimal was 0.5 when the WTP approximated CA$400,000/QALY. CONCLUSIONS: The ICURs of anti-TNF-α drugs were not satisfactory in treating patients with moderate-to-severe refractory UC. Future research could be aimed at the long-term clinical benefits of these drugs, especially adalimumab for patients intolerant or unresponsive to infliximab treatment. BioMed Central 2009-12-11 /pmc/articles/PMC2797497/ /pubmed/20003364 http://dx.doi.org/10.1186/1478-7547-7-20 Text en Copyright ©2009 Xie et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xie, Feng
Blackhouse, Gord
Assasi, Nazila
Gaebel, Kathryn
Robertson, Diana
Goeree, Ron
Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title_full Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title_fullStr Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title_full_unstemmed Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title_short Cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
title_sort cost-utility analysis of infliximab and adalimumab for refractory ulcerative colitis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797497/
https://www.ncbi.nlm.nih.gov/pubmed/20003364
http://dx.doi.org/10.1186/1478-7547-7-20
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