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临床 SLEDAI-2K 零可能是 SLE 研究中的一种实用的结果测量指标。

Clinical SLEDAI-2K zero may be a pragmatic outcome measure in SLE studies.

机构信息

a Division of Rheumatology, Department of Medicine , Karolinska Institutet , Stockholm , Sweden.

b Rheumatology , Karolinska University Hospital , Stockholm , Sweden.

出版信息

Expert Opin Biol Ther. 2019 Feb;19(2):157-168. doi: 10.1080/14712598.2019.1561856. Epub 2018 Dec 27.

Abstract

: Development of therapies for systemic lupus erythematosus (SLE) has in part been limited by the lack of suitable outcome measures in clinical trials. In the present post-hoc analysis of two clinical trials of belimumab, we investigated two potential outcomes, the Lupus Low Disease Activity State (LLDAS) and clinical SLE disease activity index 2000 (cSLEDAI-2K) zero, in relation to SLE responder index 4 (SRI-4). : A total of 1684 SLE patients from the BLISS-52 (n = 865) and BLISS-76 (n = 819) trials were surveyed. Physician's Global Assessment (PGA) scores <0.5 (3-point scale) were used for comparisons. We used the chi-square test for comparisons and the phi coefficient for correlations. : At week 52, LLDAS was achieved by 8.6% of patients, cSLEDAI-2K = 0 by 34.5% and SRI-4 by 45.1%. cSLEDAI-2K = 0 showed the strongest correlation with PGA <0.5 (r = 0.36, < 0.001). cSLEDAI-2K = 0 unveiled the superiority of belimumab 10 mg/kg over placebo ( = 0.003) with a magnitude which was comparable to that of SRI-4 ( < 0.001). LLDAS displayed a more moderate separation ( = 0.033). : LLDAS was a stringent measure. cSLEDAI-2K = 0 showed the strongest correlation with the clinician-based evaluation. Being based on the SLEDAI-2K only, cSLEDAI-2K = 0 may be considered a more pragmatic outcome measure in SLE studies compared with composite tools.

摘要

: 系统性红斑狼疮 (SLE) 的治疗方法的发展在一定程度上受到临床试验中缺乏合适的疗效指标的限制。在贝鲁单抗两项临床试验的事后分析中,我们研究了两种潜在的疗效指标,狼疮低疾病活动状态 (LLDAS) 和临床 SLE 疾病活动指数 2000 (cSLEDAI-2K) 为 0,与 SLE 应答指数 4 (SRI-4) 相关。 : 共调查了来自 BLISS-52 试验(n=865)和 BLISS-76 试验(n=819)的 1684 名 SLE 患者。使用医师整体评估 (PGA) 评分 <0.5(3 分制)进行比较。我们使用卡方检验进行比较,phi 系数进行相关性分析。 : 在第 52 周,8.6%的患者达到 LLDAS,34.5%的患者达到 cSLEDAI-2K=0,45.1%的患者达到 SRI-4。cSLEDAI-2K=0 与 PGA <0.5 呈最强相关性 (r=0.36, <0.001)。cSLEDAI-2K=0 揭示了贝鲁单抗 10 mg/kg 优于安慰剂的优越性(=0.003),其程度与 SRI-4 相当( <0.001)。LLDAS 显示出更适中的分离度(=0.033)。 : LLDAS 是一项严格的指标。cSLEDAI-2K=0 与基于临床医生的评估呈最强相关性。仅基于 SLEDAI-2K,cSLEDAI-2K=0 可能被认为是 SLE 研究中比综合工具更实用的疗效指标。

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