McMaster Development Consultants Ltd., Glasgow, Scotland, UK.
Value Health. 2011 Jan;14(1):15-23. doi: 10.1016/j.jval.2010.10.016.
Despite its proven efficacy, infliximab is often considered to be an expensive treatment for patients with psoriatic arthritis.
To estimate the cost-effectiveness of infliximab among patients with active and progressive psoriatic arthritis.
A decision analytic model was constructed to simulate disease progression in hypothetical cohorts of patients with psoriatic arthritis receiving infliximab maintenance treatment. The primary response measure was change in Health Assessment Questionnaire score from a baseline estimated from mixed treatment models drawn from published clinical trials. Palliative care, comprising nonbiologic disease-modifying antirheumatic drugs, was used as a comparator. The primary outcome was quality-adjusted life years. The dose of infliximab was estimated for a range of 60 to 80 kg per patient body weight. The costs and outcomes were discounted at 3.5% for a period of 40 years. Uncertainty around the results was explored with probabilistic sensitivity analysis.
The mixed treatment comparison showed a significant reduction in Health Assessment Questionnaire score across all patients. The tumor necrosis factor α inhibitors were significantly superior to palliative care but comparable with one another. The incremental cost-effectiveness ratios for etanercept, adalimumab, and infliximab relative to palliative care were £17,327; £19,246; and £16,942 to £23,022, respectively, across all patients with psoriatic arthritis and £16,613; £18,170; and £15,788 to £21,736, respectively, in the subgroup with significant psoriasis.
Infliximab represents a cost-effective treatment option well within the National Institute for Health and Clinical Excellence threshold relative to palliative care. In light of equivalent outcomes with other tumor necrosis factor α inhibitors, its position in the treatment pathway is likely to be governed by treatment costs.
尽管英夫利昔单抗已被证实有效,但对于患有银屑病关节炎的患者而言,该药通常被视为一种昂贵的治疗选择。
评估英夫利昔单抗治疗活动期和进展性银屑病关节炎患者的成本效益。
构建决策分析模型以模拟接受英夫利昔单抗维持治疗的银屑病关节炎患者队列的疾病进展情况。主要应答指标为从混合治疗模型中估算的基线健康评估问卷评分变化,这些模型来自已发表的临床试验。姑息治疗(包括非生物性疾病修正抗风湿药物)作为对照。主要结局为质量调整生命年。根据患者体重,英夫利昔单抗的剂量估计范围为 60 至 80 千克。在 40 年期间,成本和结果以 3.5%的贴现率贴现。使用概率敏感性分析探讨结果的不确定性。
混合治疗比较显示,所有患者的健康评估问卷评分均显著降低。肿瘤坏死因子-α抑制剂显著优于姑息治疗,但彼此相当。与姑息治疗相比,依那西普、阿达木单抗和英夫利昔单抗的增量成本效益比分别为 17327 英镑、19246 英镑和 16942 至 23022 英镑,所有银屑病关节炎患者的情况均如此;16613 英镑、18170 英镑和 15788 至 21736 英镑,在伴有显著银屑病的亚组患者中情况如此。
英夫利昔单抗相对于姑息治疗是一种具有成本效益的治疗选择,其成本效益比在国家卫生与临床优化研究所的阈值范围内。鉴于其他肿瘤坏死因子-α抑制剂的结局相当,其在治疗途径中的地位可能取决于治疗成本。