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使用建模方法比较瑞典基于试验数据和注册数据的英夫利昔单抗治疗类风湿关节炎的成本效益。

The comparison of trial data-based and registry data-based cost-effectiveness of infliximab treatment for rheumatoid arthritis in Sweden using a modeling approach.

机构信息

i3 Innovus, Stockholm, Sweden.

出版信息

Value Health. 2013 Mar-Apr;16(2):251-8. doi: 10.1016/j.jval.2012.11.002. Epub 2013 Jan 23.

Abstract

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 €2,400 and €24,900 to €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 €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.

摘要

目的

评估基于 3 期临床试验的预测成本效益评估在瑞典临床实践中使用英夫利昔单抗治疗类风湿关节炎的精确性。

方法

确定了 3 个患者队列:包括在英夫利昔单抗试验中的患者(ATTRACT)、从瑞典登记处最初接受英夫利昔单抗治疗的患者(STURE)、符合 ATTRACT 试验纳入标准的这些登记处患者子集是第三个患者队列;评估了与疗效数据相关的两组假设:“ATTRACT”(试验期间的疗效数据)和“STURE”(10 年的有效性数据)。此外,还通过建模方法评估了纳入对照药物安慰剂效应作为计算成本效益的基础。利用健康经济模型估算了每获得一个质量调整生命年(QALY)的成本。

结果

当使用 ATTRACT 和 STURE 假设时,三个患者队列的结果范围从成本节约到每获得一个 QALY 的成本为 2400 欧元到 24900 欧元至 26000 欧元。敏感性分析表明,纳入安慰剂效应对结果的影响最大,所有患者队列的每获得一个 QALY 的成本增加到约 50000 欧元。

结论

通过建模方法计算,临床试验中测量的英夫利昔单抗治疗效果和临床实践中的结果导致可比的成本效益比,而与有效性数据和所选对照药物相关的假设对结果有很大影响。这加强了基于随机临床试验数据的早期建模研究的价值,但需要仔细评估所做的假设。

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