Cost-effectiveness of ustekinumab in moderate to severe Crohn's disease in Sweden

被引:3
|
作者
Hansson-Hedblom, Amanda [1 ]
Almond, Chrissy [2 ]
Borgstrom, Fredrik [1 ]
Sly, Indeg [2 ]
Enkusson, Dana [3 ]
Buchholt, Anders Troelsgaard [3 ]
Karlsson, Linda [1 ]
机构
[1] Quantify Res AB, Stockholm, Sweden
[2] BresMed, Sheffield, S Yorkshire, England
[3] Janssen Cilag AB, Solna, Sweden
关键词
Crohn's disease; Ustekinumab; Adalimumab; Vedolizumab; Cost-effectiveness; INFLAMMATORY-BOWEL-DISEASE; VEDOLIZUMAB INDUCTION THERAPY; MAINTENANCE THERAPY; ULCERATIVE-COLITIS; RANDOMIZED-TRIAL; UNITED-KINGDOM; ACTIVITY INDEX; ADALIMUMAB; STATES; ALPHA;
D O I
10.1186/s12962-018-0114-y
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Human monoclonal antibody ustekinumab is a novel Crohn's disease (CD) treatment blocking proinflammatory 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: -(sic)6984, QALYs: + 0.232). In TNF-alpha-inhibitor failure population ustekinumab accrued 0.133 more QALYs than vedolizumab, yielding a (sic)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 (sic)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.
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页数:12
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