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新疗效指标(NEDA、MEDA和延迟6个月的NEDA)在复发缓解型多发性硬化症中的5年和7年预后价值。

Five- and seven-year prognostic value of new effectiveness measures (NEDA, MEDA and six-month delayed NEDA) in relapsing-remitting multiple sclerosis.

作者信息

Tsantes Elena, Curti Erica, Collura Filippo, Bazzurri Veronica, Fiore Alessia, Granella Franco

机构信息

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, Parma, Italy.

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, Parma, Italy.

出版信息

J Neurol Sci. 2020 Jul 15;414:116827. doi: 10.1016/j.jns.2020.116827. Epub 2020 Apr 8.

Abstract

The concept of 'no evidence of disease activity' (NEDA) has been proposed as a surrogate marker for treatment response in relapsing-remittent multiple sclerosis (MS). However, there is no agreement regarding its prognostic value, nor about the starting time for evaluation of drug effectiveness. Aim of this study was to investigate if the status preservation of two-year NEDA, 'minimal evidence of disease activity' (MEDA) and six-month delayed NEDA (6md-NEDA, with a "rebaseline" six months after the treatment start) predicts the achievement of long-term disability outcomes (EDSS score ≥ 4.0 or 6.0, 3-month confirmed disability progression (CDP) or conversion to secondary progressive MS) after five and seven years of disease. A total of 271 treatment courses (TCs) were analyzed in this retrospective study, involving all TCs started with any disease-modifying treatments (DMT). Overall, 72 (27%), 77 (28%) and 92 (34%) TCs maintained NEDA, MEDA and 6md-NEDA status after a two-year treatment. NEDA, MEDA and 6md-NEDA TCs had a lower risk of attaining all disability outcomes, compared to 'evidence of disease activity' (EDA) TCs. NEDA status determined a lower risk of CDP after five (OR 0.18, 95% CI 0.07-0.45, p < .0001) and seven years of disease (OR 0.15, 95% CI 0.05-0.44, p < .0001), with high positive (90%) and low negative (42%) predictive value, good specificity and low sensitivity. NEDA TCs had a lower risk of CDP compared to MEDA TCs after seven years (OR 0.30, 95% CI 0.10-0.91, p = .04). 6md-NEDA had a small impact on the improvement of NEDA prognostic value.

摘要

“无疾病活动证据”(NEDA)的概念已被提出作为复发缓解型多发性硬化症(MS)治疗反应的替代标志物。然而,关于其预后价值以及药物疗效评估的起始时间尚无定论。本研究的目的是调查两年期NEDA、“最小疾病活动证据”(MEDA)和六个月延迟NEDA(6md-NEDA,治疗开始后六个月“重新设定基线”)的状态维持情况是否能预测疾病五年和七年后长期残疾结局(扩展残疾状态量表(EDSS)评分≥4.0或6.0、三个月确诊残疾进展(CDP)或转变为继发进展型MS)的达成情况。在这项回顾性研究中,共分析了271个治疗疗程(TCs),涉及所有起始使用任何疾病修饰治疗(DMT)的TCs。总体而言,72个(27%)、77个(28%)和92个(34%)TCs在两年治疗后维持了NEDA、MEDA和6md-NEDA状态。与“疾病活动证据”(EDA)TCs相比,NEDA、MEDA和6md-NEDA TCs达到所有残疾结局的风险较低。NEDA状态在疾病五年(比值比(OR)0.18,95%置信区间(CI)0.07 - 0.45,p <.0001)和七年(OR 0.15,95% CI 0.05 - 0.44,p <.0001)后确定了较低的CDP风险,具有高阳性(90%)和低阴性(42%)预测价值、良好的特异性和低敏感性。七年时,NEDA TCs与MEDA TCs相比具有较低的CDP风险(OR 0.30,95% CI 0.10 - 0.91,p = 0.04)。6md-NEDA对NEDA预后价值的改善影响较小。

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