Frankfurt School of Finance and Management, Adickesallee 32-34, 60322, Frankfurt am Main, Germany.
SIBE, Graduate School of the Faculty for Leadership and Management, Steinbeis University, Berlin, Germany.
Appl Health Econ Health Policy. 2020 Feb;18(1):109-125. doi: 10.1007/s40258-019-00523-1.
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.
The purpose of this study was to conduct a cost-utility analysis of secukinumab in three adult populations with active PsA in Germany: biologic naïve without moderate or severe plaque psoriasis, biologic naïve 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.
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.
In the biologic-naïve 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-naïve 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.
Secukinumab appears to be cost effective compared with other DMARDs for the treatment of active PsA in biologic-naïve and biologic-experienced populations in Germany.
银屑病关节炎(PsA)是一种慢性炎症性关节炎,发生在患有自身免疫性疾病银屑病的人群中。在德国,尚未评估司库奇尤单抗治疗银屑病关节炎的成本效益。
本研究旨在对德国三种成人活动性银屑病关节炎人群(生物初治且无中重度斑块状银屑病、生物初治且中重度斑块状银屑病、生物制剂治疗后)使用司库奇尤单抗进行成本-效用分析:比较药物包括其他疾病修饰抗风湿药物(DMARDs),包括生物类似药和标准治疗。
本分析从德国法定健康保险的角度出发。我们采用决策分析半马尔可夫模型,在终生时间范围内评估司库奇尤单抗的成本效益。根据 12 周时的银屑病关节炎反应标准评估治疗反应。未应答者或初始 DMARD 停药者可转为后续 DMARD。模型输入参数(银屑病面积严重程度指数、健康评估问卷(HAQ)、退出率、成本和资源使用)来自临床试验、已发表文献和官方报告。健康效益用质量调整生命年来表示。成本和效益采用 3%的年贴现率。通过敏感性分析评估研究结果的稳健性。
在无中重度斑块状银屑病的生物初治人群中,司库奇尤单抗 150mg 严格优于其他 DMARD(依那西普、戈利木单抗和乌司奴单抗)或具有更优的增量成本效益比(ICER)(优于依那西普、阿达木单抗和英夫利昔单抗)。在伴有中重度斑块状银屑病的生物初治人群和生物制剂治疗后人群中,司库奇尤单抗 300mg 比其他 DMARD 更有效,ICER 更低,因此具有更长的优势。确定性敏感性分析表明,结果对成本和健康结果的贴现率以及效用值输入的 HAQ 评分最为敏感。
在德国,与其他 DMARD 相比,司库奇尤单抗在生物初治和生物制剂治疗后人群中治疗活动性银屑病关节炎具有成本效益。