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首页> 外文期刊>Applied health economics and health policy >Cost Effectiveness of Secukinumab Versus Other Biologies and Apremilast in the Treatment of Active Psoriatic Arthritis in Germany
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Cost Effectiveness of Secukinumab Versus Other Biologies and Apremilast in the Treatment of Active Psoriatic Arthritis in Germany

机译:Secukinumab与其他生物学和Apremilast在德国活性银屑病关节炎的成本效果

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Introduction Psoriatic arthritis (PsA) is a chronic inflammatory arthritis that occurs in people affected by the autoimmune disease psoriasis. The cost effectiveness of secukinumab in PsA has not been evaluated in Germany. Objective The purpose of this study was to conduct a cost-utility analysis of secukinumab in three adult populations with active PsA in Germany: biologic naive without moderate or severe plaque psoriasis, biologic naive with moderate or severe plaque psoriasis, and biologic experienced. Comparators included other disease-modifying antirheumatic drugs (DMARDs), including biosimilar versions as well as standard of care. Methods The analysis took the viewpoint of the German statutory health insurance. We adapted a decision analytic semi-Markov model to evaluate the cost effectiveness of secukinumab over a lifetime horizon. Treatment response was assessed based on PsA Response Criteria at 12 weeks. Nonresponders or patients discontinuing the initial-line DMARD were allowed to switch to subsequent-line DMARDs. Model input parameters (Psoriasis Area Severity Index, Health Assessment Questionnaire (HAQ), withdrawal rates, costs, and resource use) were collected from clinical trials, published literature, and official reports. Health benefits were expressed as quality-adjusted life-years. An annual discount rate of 3% was applied to costs and benefits. The robustness of the study findings was evaluated via sensitivity analyses. Results In the biologic-naive population without moderate or severe plaque psoriasis, secukinumab 150 mg either strictly dominated other DMARDs (certolizumab pegol, golimumab, and ustekinumab) or yielded favorable incremental cost-effectiveness ratios (ICERs) (vs. etanercept, adalimumab, and infliximab). In the biologic-naive population with concomitant moderate to severe plaque psoriasis and in the biologic-experienced population, secukinumab 300 mg was more effective and had a lower ICER than other DMARDs, thus leading to extended dominance. Deterministic sensitivity analyses indicated that the results were most sensitive to the discount rate for costs and health outcomes as well as the HAQ score as an input to utility values. Conclusions Secukinumab appears to be cost effective compared with other DMARDs for the treatment of active PsA in biologic-naive and biologic-experienced populations in Germany.
机译:简介银屑病关节炎(PSA)是一种慢性炎症性关节炎,发生受自身免疫性疾病牛皮癣影响的人们。德国尚未评估Secukinumab在PSA中的成本效益。目的本研究的目的是在德国有活性PSA的三个成年人群中对Secukinumab进行的成本实用性分析:生物学天真,没有中度或严重的斑块性牛皮癣,具有中度或严重的斑块牛皮癣的生物学天真,以及生物学。比较器包括其他疾病改性的抗抗火药物(DMARDS),包括生物仿制版和护理标准。方法采取了德国法定健康保险的观点。我们改编了决策分析半标率模型,以评估Secukinumab在寿命范围内的成本效益。根据PSA响应标准在12周内评估治疗响应。不反应的人或在初始线DMARD中停止的患者被允许切换到后续线DMARDS。从临床试验,出版文学和官方报告中收集了模型输入参数(牛皮癣面积严重性指数,健康评估问卷(HAQ),撤销率,成本和资源使用)。健康福利被表达为质量调整的寿命。每年贴现3%的成本和福利。通过敏感性分析评估研究结果的稳健性。结果在没有中度或严重牙菌斑的生物学 - 幼稚牛皮癣中,Secukinumab 150mg严格统治其他DMARD(Certolizumab Pegol,Golimumab和Ustekinumab)或产生有利的增量成本效率比率(算术)(VsAnercept,Adalimalab,和英夫利昔单抗)。在生物幼稚人群中,伴随着严重的斑块牛皮癣和生物学经历的人群,Secukinumab 300毫克更有效并且比其他DMARD较低,因此导致延长的优势。确定性敏感性分析表明,结果对成本和健康结果的贴现率最敏感,以及作为效用价值的输入的哈克得分。结论Secukinumab与其他DMARD在德国生物学 - 天真和生物学矿物中的活性PSA治疗活性PSA相比,Secukinumab似乎具有成本效益。

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