Harvard Stephanie, Guh Daphne, Bansback Nick, Richette Pascal, Saraux Alain, Fautrel Bruno, Anis Aslam
University of British Columbia, Vancouver, Canada.
Centre for Health Evaluation and Outcome Sciences, 588-1081, Burrard Street, Vancouver, BC V6Z 1Y6 Canada.
Cost Eff Resour Alloc. 2017 Sep 7;15:20. doi: 10.1186/s12962-017-0081-8. eCollection 2017.
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.
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.
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).
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.
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。
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。
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)。
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。