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SLE 中 EQ-5D-3L 指数评分的区分度和已知组有效性的敏感性分析:引入“充分健康状态”。

Sensitivity analysis of EQ-5D-3L index scores in terms of discriminative and known-groups validity in SLE: introducing Adequate Health State.

机构信息

Division of Rheumatology, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.

The Swedish Rheumatism Association, Stockholm, Sweden.

出版信息

Rheumatology (Oxford). 2023 Dec 1;62(12):3916-3923. doi: 10.1093/rheumatology/kead140.

Abstract

OBJECTIVES

To investigate the ability of different EuroQol 5-Dimensions 3-Levels (EQ-5D-3L) index scores to discriminate between verum drug and placebo (discriminant validity) as well as between responders and non-responders (known-groups validity) in the SLE patient population of two phase III clinical trials of belimumab.

METHODS

Data from the BLISS-52 (NCT00424476) and BLISS-76 (NCT00410384) trials (N = 1684), which both showed superiority of belimumab to placebo, were utilized. Responders were defined as SLE Responder Index 4 (SRI-4) achievers at week 52. The Pearson's χ2 and Mann-Whitney U tests were used for comparisons, and logistic regression analysis was used for adjustments for confounders and assessment of independence.

RESULTS

While full health state (FHS; EQ-5D index score 1) showed the best ability to discriminate between belimumab and placebo [adjusted odds ratio (OR) 1.47; 95% CI 1.11, 1.96; P = 0.008] and between SRI-4 responders and non-responders (adjusted OR 3.47; 95% CI 1.29, 10.98; P = 0.020), the discriminative ability of EQ-5D index scores 0.800 or more reached statistical significance for both discriminant validity (adjusted OR 1.29; 95% CI 1.02, 1.63; P = 0.036) and known-groups validity (adjusted OR 3.08; 95% CI 1.16, 9.69; P = 0.034).

CONCLUSION

Overall, higher EQ-5D index scores were associated with increasing ability to discriminate between belimumab and placebo, and between responders and non-responders. EQ-5D index scores less stringent than FHS may be clinically relevant health-related quality of life goals of treatment in patients with SLE, introducing the concept of EQ-5D adequate health state when FHS is not achievable.

摘要

目的

评估不同欧洲五维健康量表 3 级(EQ-5D-3L)指数评分在两项贝利尤单抗 III 期临床试验 SLE 患者人群中的辨别能力(区分效度),即真药与安慰剂之间(区分效度),以及应答者与无应答者之间(已知组效度)。

方法

利用 BLISS-52(NCT00424476)和 BLISS-76(NCT00410384)试验的数据(N=1684),这两项试验均显示贝利尤单抗优于安慰剂。应答者定义为在第 52 周时达到 SLE 应答指数 4(SRI-4)的患者。采用 Pearson's χ2 检验和 Mann-Whitney U 检验进行比较,采用逻辑回归分析进行混杂因素调整,并评估独立性。

结果

虽然完全健康状态(FHS;EQ-5D 指数评分 1)在区分贝利尤单抗和安慰剂方面表现最佳[校正比值比(OR)1.47;95%置信区间(CI)1.11,1.96;P=0.008],且在区分 SRI-4 应答者和无应答者方面表现最佳(校正 OR 3.47;95% CI 1.29,10.98;P=0.020),但 EQ-5D 指数评分等于或大于 0.800 对区分效度(校正 OR 1.29;95% CI 1.02,1.63;P=0.036)和已知组效度(校正 OR 3.08;95% CI 1.16,9.69;P=0.034)也具有统计学意义。

结论

总体而言,EQ-5D 指数评分越高,区分贝利尤单抗和安慰剂以及区分应答者和无应答者的能力越强。与 FHS 相比,EQ-5D 指数评分不那么严格可能是 SLE 患者治疗的更具临床意义的健康相关生活质量目标,当无法实现 FHS 时引入 EQ-5D 充分健康状态的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3387/10691928/59e67689b498/kead140f1.jpg

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