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 |
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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. Oct/Nov 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904,30978</link.rule.ids></links><search><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><title>The Cost-Effectiveness of Ustekinumab in Moderate to Severely Active Crohn’s Disease in Sweden</title><title>Value in health</title><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.</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 & 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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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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