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多发性硬化症患者强化治疗与早期高效治疗的获益与风险。

The benefits and risks of escalation versus early highly effective treatment in patients with multiple sclerosis.

机构信息

Department of Neurology, Neurological Institute, Cleveland Clinic, Cleveland, OH, USA.

Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK.

出版信息

Expert Rev Neurother. 2023 May;23(5):433-444. doi: 10.1080/14737175.2023.2208347. Epub 2023 May 15.

Abstract

INTRODUCTION

Multiple sclerosis is a chronic, demyelinating, inflammatory, and neurodegenerative disease of the central nervous system that affects over 2 million people worldwide. Considerable advances have been made in the availability of disease modifying therapies for relapsing-remitting multiple sclerosis since their introduction in the 1990s. This has led to debate regarding the optimal first-line treatment approach: a strategy of escalation versus early highly effective treatment.

AREAS COVERED

This review defines the strategies of escalation and early highly effective treatment, outlines the pros and cons of each, and provides an analysis of both the current literature and expected future directions of the field.

EXPERT OPINION

There is growing support for using early highly effective treatment as the initial therapeutic approach in relapsing-remitting multiple sclerosis. However, much of this support stems from observational real-world studies that use historic data and lack safety outcomes or randomized control trials that compare individual high versus low-moderate efficacy therapies, instead of the approaches themselves. Randomized control trials (DELIVER-MS, TREAT-MS) are needed to systemically and prospectively compare contemporary escalation versus early highly effective treatment approaches.

摘要

简介

多发性硬化症是一种慢性脱髓鞘、炎症和神经退行性疾病,影响着全球超过 200 万人。自 20 世纪 90 年代问世以来,用于治疗复发缓解型多发性硬化症的疾病修正疗法已有了相当大的进展。这引发了关于最佳一线治疗方法的争论:升级策略与早期高效治疗。

涵盖领域

本文定义了升级和早期高效治疗策略,概述了每种策略的优缺点,并对当前文献和该领域的预期未来方向进行了分析。

专家意见

越来越多的人支持将早期高效治疗作为复发缓解型多发性硬化症的初始治疗方法。然而,这种支持主要来自于使用历史数据的观察性真实世界研究,缺乏安全性结果,也缺乏比较高与低-中度疗效治疗的随机对照试验,而不是比较这些方法本身。需要进行随机对照试验(DELIVER-MS、TREAT-MS),以系统地和前瞻性地比较当代升级与早期高效治疗方法。

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