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Modelling Cost-Effectiveness of Biologic Treatments Based on Disease Activity Scores for the Management of Rheumatoid Arthritis in Spain

机译:基于疾病活动度评分的西班牙类风湿关节炎生物治疗成本效益模型

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摘要

Background. The objective of this simulation model was to assess the cost-effectiveness of different biological treatment strategies based on levels of disease activity in Spain, in patients with moderate to severe active RA and an insufficient response to at least one anti-TNF agent. Methods. Clinically meaningful effectiveness criteria were defined using DAS28 scores: remission and Low Disease Activity State (LDAS) thresholds. Monte-Carlo simulations were conducted to assess cost-effectiveness over 2 years of four biological sequential strategies composed of anti-TNF agents (adalimumab, infliximab), abatacept or rituximab, in patients with moderate to severe active RA and an insufficient response to etanercept as first biological agent. Results. The sequential strategy including etanercept, abatacept and adalimumab appeared more efficacious over 2 years (102 days in LDAS) compared to the same sequence including rituximab as second biological option (82 days in LDAS). Cost-effectiveness ratios showed lower costs per day in LDAS with abatacept (427 €) compared to rituximab as second biological option (508 €). All comparisons were confirmed when using remission criteria. Conclusion. Model results suggest that in patients with an insufficient response to anti-TNF agents, the biological sequences including abatacept appear more efficacious and cost-effective than similar sequences including rituximab or cycled anti-TNF agents.
机译:背景。该模拟模型的目的是根据西班牙的疾病活动水平,中度至重度活动性RA和对至少一种抗TNF药物反应不足的患者,评估不同生物治疗策略的成本效益。方法。使用DAS28评分定义了具有临床意义的有效性标准:缓解和疾病低活动状态(LDAS)阈值。在中度至重度活动性RA以及对依那西普反应不足的患者中,进行了蒙特卡洛模拟评估,评估了由抗TNF药物(阿达木单抗,英夫利昔单抗),阿巴西普或利妥昔单抗组成的四种生物学顺序策略在2年内的成本效益。第一生物制剂。结果。与包括利妥昔单抗作为第二种生物学选择的相同序列(LDAS中为82天)相比,包括依那西普,阿巴西普和阿达木单抗在内的顺序策略在2年内(在LDAS中为102天)显得更有效。成本效益比显示,与第二种生物治疗方案利妥昔单抗(508欧元)相比,使用阿巴西普的LDAS每天的成本较低(427欧元)。使用缓解标准时,所有比较均得到确认。结论。模型结果表明,在对抗TNF药物反应不足的患者中,包括阿巴西普的生物学序列比包括利妥昔单抗或循环的抗TNF药物的相似序列更有效和更具成本效益。

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