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奥瑞珠单抗或那他珠单抗治疗早期高活动度复发缓解型多发性硬化症患者的 NEDA-3 达标。

NEDA-3 achievement in early highly active relapsing remitting multiple sclerosis patients treated with Ocrelizumab or Natalizumab.

机构信息

Second Division of Neurology, University of Campania Luigi Vanvitelli - Naples, Italy.

Department of Health Sciences, Section of Biostatistics, University of Genoa, Genoa, Italy.

出版信息

Mult Scler Relat Disord. 2024 Jul;87:105594. doi: 10.1016/j.msard.2024.105594. Epub 2024 Apr 6.

Abstract

BACKGROUND

in the early stages of Multiple Sclerosis (MS), initiating high-efficacy disease-modifying therapy (HE DMTs) may represent an optimal strategy for delaying neurological damage and long-term disease progression, especially in highly active MS patients (HAMS). Natalizumab (NAT) and Ocrelizumab (OCR) are recognized as HE DMTs with significant anti-inflammatory effects. This study investigates NEDA-3 achievement in treatment-naïve HAMS patients receiving NAT or OCR over three years.

METHODS

we retrospectively enrolled treatment-naïve HAMS patients undergoing NAT or OCR, collecting demographic, clinical, and instrumental data before and after treatment initiation to compare with propensity score analysis disease activity, time to disability worsening, and NEDA-3 achievement.

RESULTS

we recruited 281 HAMS patients with a mean age of 32.7 years (SD 10.33), treated with NAT (157) or OCR (124). After three years, the Kaplan-Meier probability of achieving NEDA-3 was 66.0 % (95 % CI: 57.3 % - 76.0 %) with OCR and 68.2 % (95 % CI: 59.9 % - 77.7 %) with NAT without significant differences between the two groups (p = 0.27) DISCUSSION AND CONCLUSION: starting HE DMT with monoclonal antibodies for HAMS could achieve NEDA-3 in a high percentage of patients without differences between NAT or OCR.

摘要

背景

在多发性硬化症(MS)的早期阶段,启动高效疾病修正治疗(HE DMT)可能代表着延迟神经损伤和长期疾病进展的最佳策略,尤其是在高度活跃的 MS 患者(HAMS)中。那他珠单抗(NAT)和奥瑞珠单抗(OCR)被认为是具有显著抗炎作用的 HE DMT。本研究旨在探讨三年期间接受 NAT 或 OCR 治疗的初治 HAMS 患者实现 NEDA-3 的情况。

方法

我们回顾性纳入了接受 NAT 或 OCR 治疗的初治 HAMS 患者,收集治疗前后的人口统计学、临床和仪器数据,并进行倾向评分分析,比较疾病活动度、残疾进展时间和 NEDA-3 达标情况。

结果

我们共招募了 281 名平均年龄为 32.7 岁(标准差 10.33)的 HAMS 患者,其中 157 名接受了 NAT 治疗,124 名接受了 OCR 治疗。三年后,OCR 组实现 NEDA-3 的 Kaplan-Meier 概率为 66.0%(95%CI:57.3%-76.0%),NAT 组为 68.2%(95%CI:59.9%-77.7%),两组之间无显著差异(p=0.27)。

讨论和结论

初治 HAMS 患者使用单克隆抗体启动 HE DMT 可使大部分患者实现 NEDA-3,且 NAT 和 OCR 之间无差异。

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