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脊柱关节炎中抗TNF药物的准入标准:对1年比较性成本效益估计的影响

Access criteria for anti-TNF agents in spondyloarthritis: influence on comparative 1-year cost-effectiveness estimates.

作者信息

Harvard Stephanie, Guh Daphne, Bansback Nick, Richette Pascal, Saraux Alain, Fautrel Bruno, Anis Aslam

机构信息

University of British Columbia, Vancouver, Canada.

Centre for Health Evaluation and Outcome Sciences, 588-1081, Burrard Street, Vancouver, BC V6Z 1Y6 Canada.

出版信息

Cost Eff Resour Alloc. 2017 Sep 7;15:20. doi: 10.1186/s12962-017-0081-8. eCollection 2017.

Abstract

BACKGROUND

Anti-tumor necrosis factor (anti-TNF) agents are an effective, but costly, treatment for spondyloarthritis (SpA). Worldwide, multiple sets of access criteria aim to restrict anti-TNF therapy to patients with specific clinical characteristics, yet the influence of access criteria on anti-TNF cost-effectiveness is unknown. Our objective was to use data from the DESIR cohort, a prospective study of early SpA patients in France, to determine whether the French anti-TNF access criteria are the most cost-effective in that setting relative to other potential restrictions.

METHODS

We used data from the DESIR cohort to create five study populations of patients meeting anti-TNF access criteria from Canada, France, Germany, United Kingdom, and Hong Kong, respectively. For each study population, we calculated the costs and quality-adjusted life years (QALYs) over 1 year of patients treated and not treated with anti-TNF therapy. To control for differences between anti-TNF users and non-users, we used linear regression models to derive adjusted mean costs and QALYs. We calculated incremental cost-effectiveness ratios (ICERs) representing the incremental cost per additional QALY gained by treating with an anti-TNF within each of the five study populations, using bootstrapping to explore the range of uncertainty in costs and QALYs. A series of sensitivity analyses was conducted, including one to simulate the effect of a 24-week stopping rule for anti-TNF non-responders.

RESULTS

Anti-TNF access criteria from France were satisfied by the largest proportion of DESIR patients (27.8%), followed by Germany (25.1%), Canada (23.8%), the UK (12.1%) and Hong Kong (8.6%). Confidence intervals around incremental costs and QALYs in the basecase analysis were overlapping, indicating that anti-TNF cost-effectiveness estimates derived from each subset were similar. In the sensitivity analysis that examined the effect of excluding costs accumulated past 24 weeks by anti-TNF non-responders, the incremental cost per QALY was reduced by approximately 25% relative to the basecase analysis (France: €857,992 vs. €1,105,859; Canada: € 626,459 vs. €818,186; Germany: € 422,568 vs. €545,808); UK €578,899 vs. €766,217; Hong Kong €335,418 vs. €456,850).

CONCLUSIONS

Anti-TNF cost-effectiveness is strongly affected by treatment continuation among non-responders. Access criteria could improve anti-TNF cost-effectiveness by defining patients likely to respond.

摘要

背景

抗肿瘤坏死因子(抗TNF)药物是治疗脊柱关节炎(SpA)的一种有效但昂贵的疗法。在全球范围内,多套准入标准旨在将抗TNF治疗限制于具有特定临床特征的患者,但准入标准对抗TNF成本效益的影响尚不清楚。我们的目标是利用法国早期SpA患者前瞻性研究DESIR队列的数据,确定法国抗TNF准入标准在该环境下相对于其他潜在限制措施是否最具成本效益。

方法

我们使用DESIR队列的数据,分别创建了符合加拿大、法国、德国、英国和香港抗TNF准入标准的五个患者研究群体。对于每个研究群体,我们计算了接受和未接受抗TNF治疗的患者1年内的成本和质量调整生命年(QALY)。为了控制抗TNF使用者和非使用者之间的差异,我们使用线性回归模型得出调整后的平均成本和QALY。我们计算了增量成本效益比(ICER),代表在五个研究群体中每个群体使用抗TNF治疗每多获得一个QALY所增加的成本,使用自抽样法探索成本和QALY的不确定性范围。进行了一系列敏感性分析,包括一项模拟对抗TNF无反应者采用24周停药规则的效果的分析。

结果

DESIR患者中满足法国抗TNF准入标准的比例最高(27.8%),其次是德国(25.1%)、加拿大(23.8%)、英国(12.1%)和香港(8.6%)。基础病例分析中增量成本和QALY周围的置信区间相互重叠,表明从每个亚组得出的抗TNF成本效益估计相似。在敏感性分析中,研究了排除抗TNF无反应者24周后累积成本的影响,相对于基础病例分析,每QALY的增量成本降低了约25%(法国:857,992欧元对1,105,859欧元;加拿大:626,459欧元对818,186欧元;德国:422,568欧元对545,808欧元;英国:578,899欧元对766,217欧元;香港:335,418欧元对456,850欧元)。

结论

抗TNF的成本效益受无反应者持续治疗的强烈影响。准入标准可通过定义可能有反应的患者来提高抗TNF的成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5596/5590198/4b568304465b/12962_2017_81_Fig1_HTML.jpg

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