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The Comparison of Trial Data-Based and Registry Data-Based Cost-Effectiveness of Infliximab Treatment for Rheumatoid Arthritis in Sweden Using a Modeling Approach

机译:瑞典英夫利昔单抗治疗类风湿性关节炎的试验数据和注册数据成本效益的比较使用建模方法

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摘要

Objective: To evaluate the precision of the predictive cost-effectiveness assessment based on a phase 3 clinical trial with infliximab for the treatment of rheumatoid arthritis in Swedish clinical practice. Methods: Three patient cohorts were identified: the patients included in the infliximab trial (ATTRACT), patients initially treated with infliximab from a Swedish registry (STURE), a subset of these registry patients meeting inclusion criteria for the ATTRACT trial was the third patient cohort; two sets of assumptions in relation to the efficacy data were evaluated: "ATTRACT" (efficacy data over the duration of the trial) and "STURE" (effectiveness data over 10 years). In addition, the impact of including the placebo effect for the comparator was evaluated as a basis for the calculation of cost-effectiveness by using a modeling approach. A health economic model was utilized to estimate the cost per quality-adjusted life-year (QALY) gained. Results: The results for the three patient cohorts ranged from cost saving to a cost per QALY gained of (sic)2,400 and (sic)24,900 to (sic)26,000 when the ATTRACT and STURE assumptions were used, respectively. Sensitivity analyses indicated that the inclusion of placebo effect had the largest effect on the results, increasing the cost per QALY gained to approximately (sic)50,000 for all patient cohorts. Conclusions: The treatment effect of infliximab measured in clinical trials and clinical practice results in comparable cost-effectiveness ratios, as calculated by using a modeling approach, whereas the assumptions made in relation to the effectiveness data and the chosen comparator have a large impact on the results. This reinforces the value of early modeling studies based on randomized clinical trial data, but assumptions made need to be carefully assessed.
机译:目的:在瑞典临床实践中,基于英夫利昔单抗治疗类风湿性关节炎的3期临床试验,评估预测成本效益评估的准确性。方法:确定了三个患者队列:英夫利昔单抗试验(ATTRACT)所包括的患者,瑞典注册中心(STURE)最初接受英夫利昔单抗治疗的患者,这些符合ATTRACT试验纳入标准的注册患者中的一部分是第三组患者;评估了与功效数据有关的两组假设:“ ATTRACT”(试验期间的功效数据)和“ STURE”(10年以上的功效数据)。此外,使用建模方法评估了包括安慰剂对比较者的影响,作为计算成本效益的基础。利用健康经济模型来估算获得的每个质量调整生命年(QALY)的成本。结果:使用ATTRACT和STURE假设时,这三个患者队列的结果从节省成本到每QALY获得的成本分别为(sic)2,400和(sic)24,900到(sic)26,000。敏感性分析表明,安慰剂作用的纳入对结果的影响最大,所有患者队列的每QALY获得的费用增加至大约(sic)50,000。结论:英夫利昔单抗的治疗效果在临床试验和临床实践中得到了可比的成本-效果比,这是通过使用建模方法计算得出的,而有关效果数据和所选比较者的假设对药物的疗效有很大影响。结果。这增强了基于随机临床试验数据的早期建模研究的价值,但是需要仔细评估所做出的假设。

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