The Cost-Effectiveness of Ustekinumab in Moderate to Severely Active Crohn’s Disease in Sweden

OBJECTIVES: Human monoclonal antibody ustekinumab is a novel Crohn's disease (CD) treatment option which blocks pro-inflammatory cytokines interleukins (IL)-12 and IL-23.The aim was to assess the cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effe...

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Veröffentlicht in:Value in health 2017-10, Vol.20 (9), p.A634
Hauptverfasser: Hansson-Hedblom, A, Almond, C, Borgström, F, Sly, I, Enkusson, D, Troelsgaard Buchholt, A, Karlsson, L
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container_end_page
container_issue 9
container_start_page A634
container_title Value in health
container_volume 20
creator Hansson-Hedblom, A
Almond, C
Borgström, F
Sly, I
Enkusson, D
Troelsgaard Buchholt, A
Karlsson, L
description OBJECTIVES: Human monoclonal antibody ustekinumab is a novel Crohn's disease (CD) treatment option which blocks pro-inflammatory cytokines interleukins (IL)-12 and IL-23.The aim was to assess the cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effectiveness model with a decision tree structure for the induction phase and a Markov cohort structure for the maintenance phase was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in a conventional-care-failure population and to vedolizumab in patients previously failingTNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase III clinical trials. Maintenance and comparator efficacy came from a network meta-analysis and a treatment sequence analysis. Resource use and cost data were derived from the literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and a 2-year maximum treatment duration.The robustness of the results was tested in univariate and probabilistic sensitivity analyses (PSA). The cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in the conventional-care-failure population. The total cost was €6,984 lower for ustekinumab compared to adalimumab and the incremental QALY gain was 0.232. In theTNF-alpha-inhibitor-failure population, ustekinumab's incremental QALY gain versus vedolizumab was 0.133, at an incremental cost of €4,023, yielding an incremental cost-effectiveness ratio (ICER) of €30,282. Results were sensitive to excluding indirect costs and to increasing the treatment duration. An increased treatment duration improved cost-effectiveness versus adalimumab but increased the ICER versus vedolizumab. PSA showed that at a 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: The results indicate that ustekinumab dominates adalimumab in the conventional-care-failure population, and is cost-effective versus vedolizumab in the TNF-alpha-inhibitor-failure population.
doi_str_mv 10.1016/j.jval.2017.08.1435
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METHODS: A cost-effectiveness model with a decision tree structure for the induction phase and a Markov cohort structure for the maintenance phase was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in a conventional-care-failure population and to vedolizumab in patients previously failingTNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase III clinical trials. Maintenance and comparator efficacy came from a network meta-analysis and a treatment sequence analysis. Resource use and cost data were derived from the literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and a 2-year maximum treatment duration.The robustness of the results was tested in univariate and probabilistic sensitivity analyses (PSA). The cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in the conventional-care-failure population. The total cost was €6,984 lower for ustekinumab compared to adalimumab and the incremental QALY gain was 0.232. In theTNF-alpha-inhibitor-failure population, ustekinumab's incremental QALY gain versus vedolizumab was 0.133, at an incremental cost of €4,023, yielding an incremental cost-effectiveness ratio (ICER) of €30,282. Results were sensitive to excluding indirect costs and to increasing the treatment duration. An increased treatment duration improved cost-effectiveness versus adalimumab but increased the ICER versus vedolizumab. PSA showed that at a 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: The results indicate that ustekinumab dominates adalimumab in the conventional-care-failure population, and is cost-effective versus vedolizumab in the TNF-alpha-inhibitor-failure population.</description><identifier>ISSN: 1098-3015</identifier><identifier>EISSN: 1524-4733</identifier><identifier>DOI: 10.1016/j.jval.2017.08.1435</identifier><language>eng</language><publisher>Lawrenceville: Elsevier Science Ltd</publisher><subject>Clinical research ; Clinical trials ; Cost analysis ; Crohn's disease ; Discontinued ; Efficacy ; Experts ; Health care expenditures ; Immunoglobulins ; Immunotherapy ; Indirect costs ; Induction ; Inflammation ; Inflammatory bowel diseases ; Interleukin 23 ; Medical treatment ; Meta-analysis ; Monoclonal antibodies ; Quality adjusted life years ; Remission ; Remission (Medicine) ; Robustness ; Sensitivity analysis ; Surgery ; Tumor necrosis factor-α ; Willingness to pay</subject><ispartof>Value in health, 2017-10, Vol.20 (9), p.A634</ispartof><rights>Copyright Elsevier Science Ltd. 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METHODS: A cost-effectiveness model with a decision tree structure for the induction phase and a Markov cohort structure for the maintenance phase was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in a conventional-care-failure population and to vedolizumab in patients previously failingTNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase III clinical trials. Maintenance and comparator efficacy came from a network meta-analysis and a treatment sequence analysis. Resource use and cost data were derived from the literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and a 2-year maximum treatment duration.The robustness of the results was tested in univariate and probabilistic sensitivity analyses (PSA). The cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in the conventional-care-failure population. The total cost was €6,984 lower for ustekinumab compared to adalimumab and the incremental QALY gain was 0.232. In theTNF-alpha-inhibitor-failure population, ustekinumab's incremental QALY gain versus vedolizumab was 0.133, at an incremental cost of €4,023, yielding an incremental cost-effectiveness ratio (ICER) of €30,282. Results were sensitive to excluding indirect costs and to increasing the treatment duration. An increased treatment duration improved cost-effectiveness versus adalimumab but increased the ICER versus vedolizumab. PSA showed that at a 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: The results indicate that ustekinumab dominates adalimumab in the conventional-care-failure population, and is cost-effective versus vedolizumab in the TNF-alpha-inhibitor-failure population.</description><subject>Clinical research</subject><subject>Clinical trials</subject><subject>Cost analysis</subject><subject>Crohn's disease</subject><subject>Discontinued</subject><subject>Efficacy</subject><subject>Experts</subject><subject>Health care expenditures</subject><subject>Immunoglobulins</subject><subject>Immunotherapy</subject><subject>Indirect costs</subject><subject>Induction</subject><subject>Inflammation</subject><subject>Inflammatory bowel diseases</subject><subject>Interleukin 23</subject><subject>Medical treatment</subject><subject>Meta-analysis</subject><subject>Monoclonal antibodies</subject><subject>Quality adjusted life years</subject><subject>Remission</subject><subject>Remission (Medicine)</subject><subject>Robustness</subject><subject>Sensitivity analysis</subject><subject>Surgery</subject><subject>Tumor necrosis factor-α</subject><subject>Willingness to pay</subject><issn>1098-3015</issn><issn>1524-4733</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>7QJ</sourceid><recordid>eNotkEtOwzAURS0EEqWwAiaWGCf4l9gZVqV8pCIGbcfGcZ7VhDYudlrUGdtge6yEBBi9-6T7kQ5C15SklND8tkmbg9mkjFCZEpVSwbMTNKIZE4mQnJ_2mhQq4YRm5-gixoYQknOWjdDrcg146mOXzJwD29UHaCFG7B1exQ7e6na_NSWuW_zsKwimA9x5vIADBNgc8eQ3gafBr9vvz6-I7-oIJsIQWHxABe0lOnNmE-Hq_47R6n62nD4m85eHp-lknlhKZZYI5wpqKiVkUfLSkiwzvMi4EQJcXnErlbQAjFVSMMG4Km2Vk_6xzCllgfMxuvnr3QX_vofY6cbvQ9tPakYpl6ygsuhd_M9lg48xgNO7UG9NOGpK9IBSN3pAqQeUmig9oOQ_B6xpVQ</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Hansson-Hedblom, A</creator><creator>Almond, C</creator><creator>Borgström, F</creator><creator>Sly, I</creator><creator>Enkusson, D</creator><creator>Troelsgaard Buchholt, A</creator><creator>Karlsson, L</creator><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope></search><sort><creationdate>201710</creationdate><title>The Cost-Effectiveness of Ustekinumab in Moderate to Severely Active Crohn’s Disease in Sweden</title><author>Hansson-Hedblom, A ; Almond, C ; Borgström, F ; Sly, I ; Enkusson, D ; Troelsgaard Buchholt, A ; Karlsson, L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1175-4ff91ad8479b3bc055a3953a44ef6d3c787cee22d7424238bcd60d74c2f88ce33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Clinical research</topic><topic>Clinical trials</topic><topic>Cost analysis</topic><topic>Crohn's disease</topic><topic>Discontinued</topic><topic>Efficacy</topic><topic>Experts</topic><topic>Health care expenditures</topic><topic>Immunoglobulins</topic><topic>Immunotherapy</topic><topic>Indirect costs</topic><topic>Induction</topic><topic>Inflammation</topic><topic>Inflammatory bowel diseases</topic><topic>Interleukin 23</topic><topic>Medical treatment</topic><topic>Meta-analysis</topic><topic>Monoclonal antibodies</topic><topic>Quality adjusted life years</topic><topic>Remission</topic><topic>Remission (Medicine)</topic><topic>Robustness</topic><topic>Sensitivity analysis</topic><topic>Surgery</topic><topic>Tumor necrosis factor-α</topic><topic>Willingness to pay</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hansson-Hedblom, A</creatorcontrib><creatorcontrib>Almond, C</creatorcontrib><creatorcontrib>Borgström, F</creatorcontrib><creatorcontrib>Sly, I</creatorcontrib><creatorcontrib>Enkusson, D</creatorcontrib><creatorcontrib>Troelsgaard Buchholt, A</creatorcontrib><creatorcontrib>Karlsson, L</creatorcontrib><collection>CrossRef</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Value in health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hansson-Hedblom, A</au><au>Almond, C</au><au>Borgström, F</au><au>Sly, I</au><au>Enkusson, D</au><au>Troelsgaard Buchholt, A</au><au>Karlsson, L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Cost-Effectiveness of Ustekinumab in Moderate to Severely Active Crohn’s Disease in Sweden</atitle><jtitle>Value in health</jtitle><date>2017-10</date><risdate>2017</risdate><volume>20</volume><issue>9</issue><spage>A634</spage><pages>A634-</pages><issn>1098-3015</issn><eissn>1524-4733</eissn><abstract>OBJECTIVES: Human monoclonal antibody ustekinumab is a novel Crohn's disease (CD) treatment option which blocks pro-inflammatory cytokines interleukins (IL)-12 and IL-23.The aim was to assess the cost-effectiveness of ustekinumab in moderate to severely active CD in Sweden. METHODS: A cost-effectiveness model with a decision tree structure for the induction phase and a Markov cohort structure for the maintenance phase was constructed. CD was represented by five health-states: remission, mild, moderate-severe, surgery and death. Ustekinumab was compared to adalimumab in a conventional-care-failure population and to vedolizumab in patients previously failingTNF-alpha-inhibitor treatment. Discontinuation probabilities, utilities and ustekinumab induction efficacy were sourced from phase III clinical trials. Maintenance and comparator efficacy came from a network meta-analysis and a treatment sequence analysis. Resource use and cost data were derived from the literature and validated by clinical experts. The analysis had a societal perspective, a life-time time-horizon, and a 2-year maximum treatment duration.The robustness of the results was tested in univariate and probabilistic sensitivity analyses (PSA). The cost-effectiveness was estimated using quality-adjusted life-years (QALYs). RESULTS: Ustekinumab dominated adalimumab in the conventional-care-failure population. The total cost was €6,984 lower for ustekinumab compared to adalimumab and the incremental QALY gain was 0.232. In theTNF-alpha-inhibitor-failure population, ustekinumab's incremental QALY gain versus vedolizumab was 0.133, at an incremental cost of €4,023, yielding an incremental cost-effectiveness ratio (ICER) of €30,282. Results were sensitive to excluding indirect costs and to increasing the treatment duration. An increased treatment duration improved cost-effectiveness versus adalimumab but increased the ICER versus vedolizumab. PSA showed that at a 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: The results indicate that ustekinumab dominates adalimumab in the conventional-care-failure population, and is cost-effective versus vedolizumab in the TNF-alpha-inhibitor-failure population.</abstract><cop>Lawrenceville</cop><pub>Elsevier Science Ltd</pub><doi>10.1016/j.jval.2017.08.1435</doi><oa>free_for_read</oa></addata></record>
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source Elsevier ScienceDirect Journals; Applied Social Sciences Index & Abstracts (ASSIA); EZB-FREE-00999 freely available EZB journals
subjects Clinical research
Clinical trials
Cost analysis
Crohn's disease
Discontinued
Efficacy
Experts
Health care expenditures
Immunoglobulins
Immunotherapy
Indirect costs
Induction
Inflammation
Inflammatory bowel diseases
Interleukin 23
Medical treatment
Meta-analysis
Monoclonal antibodies
Quality adjusted life years
Remission
Remission (Medicine)
Robustness
Sensitivity analysis
Surgery
Tumor necrosis factor-α
Willingness to pay
title The Cost-Effectiveness of Ustekinumab in Moderate to Severely Active Crohn’s Disease in Sweden
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