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从加拿大角度评估司库奇尤单抗治疗强直性脊柱炎的成本效果。

Cost-effectiveness analysis of secukinumab in ankylosing spondylitis from the Canadian perspective.

机构信息

a Goeree Consulting Ltd and Professor Emeritus, McMaster University , Hamilton , Ontario , Canada.

b Novartis Pharmaceuticals Canada Inc. , Dorval , Quebec , Canada.

出版信息

J Med Econ. 2019 Jan;22(1):45-52. doi: 10.1080/13696998.2018.1539400. Epub 2018 Nov 13.

Abstract

AIM

To assess the cost-effectiveness of interleukin (IL)-17A inhibitor secukinumab vs the currently licensed biologic therapies in ankylosing spondylitis (AS) patients from a Canadian healthcare system perspective.

METHODS

A decision analytic model (semi-Markov) evaluated the cost-effectiveness of secukinumab 150 mg compared to certolizumab pegol, adalimumab, golimumab, etanercept and etanercept biosimilar, and infliximab and infliximab biosimilar in a biologic-naïve population, over 60 years of time horizon (lifetime). The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI 50) response rate was used to assess treatment response at week 12. Non-responders or patients discontinuing initial-line of biologic therapy were allowed to switch to subsequent-line biologics. Model input parameters (short-term and long-term changes in BASDAI and Bath Ankylosing Spondylitis Functional Index [BASFI], withdrawal rates, adverse events, costs, resource use, utilities, and disutilities) were obtained from clinical trials, published literature, and other Canadian sources. Benefits were expressed as quality-adjusted life years (QALYs). Cost and benefits were discounted with an annual discount rate of 1.5% for all treatments.

RESULTS

In the biologic-naïve population, secukinumab 150 mg dominated all comparators, as patients treated with secukinumab 150 mg achieved the highest QALYs (16.46) at the lowest cost (CAD 533,010) over a lifetime horizon vs comparators. In the deterministic sensitivity analysis, results were most sensitive to changes in baseline BASFI non-responders, BASDAI 50 at 3 months and discount rates. Probabilistic sensitivity analysis showed that secukinumab 150 mg demonstrated higher probability of achieving maximum net monetary benefit vs all comparators at various cost thresholds.

CONCLUSIONS

This analysis demonstrates that secukinumab 150 mg is the most cost-effective treatment option for biologic-naïve AS patients compared to certolizumab pegol, adalimumab, golimumab, etanercept and etanercept biosimilar, and infliximab and infliximab biosimilar for a lifetime horizon in Canada. Treatment with secukinumab translates into substantial benefits for patients and the healthcare system.

摘要

目的

从加拿大医疗保健系统的角度评估白细胞介素(IL)-17A 抑制剂司库奇尤单抗与目前已获许可的生物疗法在强直性脊柱炎(AS)患者中的成本效益。

方法

通过半马尔可夫决策分析模型评估了在 60 年时间范围内(终生),与培塞利珠单抗、阿达木单抗、戈利木单抗、依那西普和依那西普生物类似药以及英夫利昔单抗和英夫利昔单抗生物类似药相比,150mg 司库奇尤单抗在生物初治人群中的成本效益。使用巴斯强直性脊柱炎疾病活动指数(BASDAI 50)缓解率来评估第 12 周的治疗反应。未应答或停止初始生物治疗的患者允许转换为后续生物治疗。模型输入参数(短期和长期 BASDAI 和巴斯强直性脊柱炎功能指数 [BASFI]变化、退出率、不良事件、成本、资源使用、效用和非效用)来自临床试验、已发表的文献和其他加拿大来源。益处表示为质量调整生命年(QALY)。所有治疗均以每年 1.5%的贴现率贴现成本和收益。

结果

在生物初治人群中,司库奇尤单抗 150mg 优于所有对照药物,因为接受司库奇尤单抗 150mg 治疗的患者在终生期间获得了最高的 QALY(16.46),而成本最低(CAD533010)。在确定性敏感性分析中,结果对基线 BASFI 无应答者、3 个月时 BASDAI50 和贴现率的变化最为敏感。概率敏感性分析表明,在各种成本阈值下,司库奇尤单抗 150mg 比所有对照药物更有可能实现最大净货币收益。

结论

这项分析表明,与培塞利珠单抗、阿达木单抗、戈利木单抗、依那西普和依那西普生物类似药以及英夫利昔单抗和英夫利昔单抗生物类似药相比,在加拿大的终生期间,司库奇尤单抗 150mg 是生物初治 AS 患者最具成本效益的治疗选择。使用司库奇尤单抗可使患者和医疗保健系统获得实质性收益。

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