Neuroimmunological and Multiple Sclerosis Clinic and Research Unit, Clinical Department of Neurology, Innsbruck Medical University, Innsbruck, Austria.
J Neurol Sci. 2009 Dec;287 Suppl 1:S37-45. doi: 10.1016/S0022-510X(09)71299-7.
Recent clinical studies in multiple sclerosis have provided new data on glatiramer acetate, interferon-beta preparations and natalizumab, which will have important implications for optimising patient care. Once a diagnosis has been made with confidence, early initiation of immunotherapy is warranted because of the presence of continuous inflammatory disease activity. Approval for therapy in patients with a clinically isolated syndrome has been granted to several first-line treatments, and most recently to glatiramer acetate. The utility of systematic frequent MRI monitoring of disease activity and response to therapy is not yet clearly established. Treatment efficacy after initiating therapy at the first demyelinating episode has to be followed carefully and re-evaluated whenever necessary. The occurrence of further relapses, confirmed disability progression or MRI evidence of persistent or aggravated disease activity would be regarded as evidence for an inadequate treatment response. However, limitations of clinical scores in faithfully reflecting disease activity at all times, as well as uncertainties about the discriminatory capacity of surrogate measures such as MRI, need to be clarified before clear-cut recommendations on treatment failure can be advocated. Escalation therapy is reserved for patients presenting with 'aggressive disease', which can be operationally defined as the occurrence of two severe relapses within twelve months, together with either MRI evidence for persistent disease activity or a two-point progression of disability on the EDSS.
最近多发性硬化症的多项临床研究提供了关于醋酸格拉替雷、干扰素-β制剂和那他珠单抗的新数据,这将对优化患者治疗产生重要影响。一旦有信心做出明确的诊断,就需要及早开始免疫治疗,因为存在持续的炎症性疾病活动。几种一线治疗药物已获准用于临床孤立综合征患者的治疗,最近又批准了醋酸格拉替雷。系统频繁进行 MRI 监测疾病活动和治疗反应的效用尚未明确确定。在首次脱髓鞘发作时开始治疗后,必须密切关注治疗效果,并在必要时重新评估。进一步复发、确认残疾进展或 MRI 显示持续或加重的疾病活动将被视为治疗反应不足的证据。然而,在能够明确提倡治疗失败之前,需要澄清临床评分在任何时候都不能忠实地反映疾病活动的局限性,以及替代指标(如 MRI)的区分能力存在不确定性。升级治疗保留给表现出“侵袭性疾病”的患者,该疾病可以通过在 12 个月内发生两次严重复发、MRI 显示持续疾病活动或 EDSS 上残疾进展两点来操作定义。