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继发进展型多发性硬化症诊断与管理中的方法及挑战:中东欧医疗专业人员视角

Approaches and challenges in the diagnosis and management of secondary progressive multiple sclerosis: A Central Eastern European perspective from healthcare professionals.

作者信息

Boyko Alexey, Therapontos Christina, Horakova Dana, Szilasiová Jarmila, Kalniņa Jolanta, Kolontareva Julia, Gross-Paju Katrin, Selmaj Krzysztof, Sereike Ieva, Milo Ron, Gabelić Tereza, Rot Uroš

机构信息

Department of Neurology, Neurosurgery and Medical Genetics, Pirogov's Russian National Research Medical University, Moscow, Russian Federation; Department of Neuropharmacology, Federal Center of Brain and Neurotechnology, Moscow, Russian Federation.

Novartis Pharma Services Inc., Cyprus.

出版信息

Mult Scler Relat Disord. 2021 May;50:102778. doi: 10.1016/j.msard.2021.102778. Epub 2021 Jan 28.

Abstract

Secondary progressive multiple sclerosis (SPMS) is a debilitating condition characterized by gradual worsening after an initial relapsing disease course. Despite the recent advances in our understanding of the disease, the diagnosis and treatment of SPMS continue to be challenging in routine clinical practice. The aim of this review article is to present the views of leading MS experts on the challenges in the diagnosis and management of SPMS and clinicians' perspectives in Central and Eastern Europe. This article also provides recommendations of MS experts to improve the situation with diagnosis and management of SPMS. Many countries within Central and Eastern Europe have high prevalence of MS (>100 per 100,000 population). Consistent with the global trend, in the absence of reliable tests or biomarkers, SPMS at early stage remains undiagnosed. Due to diagnostic uncertainty and lack of a universally accepted disease definition, clinicians rely more on retrospective analysis of the clinical symptoms to confirm the diagnosis. With the lack of awareness and poor understanding of the timing of the onset of SPMS, clinicians may tend to direct attention to relapses than the symptoms of progression, which leads to underestimation of SPMS. Although several predictors of progression to SPMS have been identified, their predictive value is highly variable. Therefore, defining the transitioning period as a separate stage of MS is essential. According to experts' opinion, frequent follow-up of patients and periodic assessment of progression are recommended for the timely identification of patients transitioning from RRMS to SPMS. MSProDiscuss Tool is an example of a quick assessment tool for identifying patients progressing from RRMS to SPMS. MS progression is usually assessed by changes in Expanded Disability Status Scale (EDSS) scores. As EDSS scores tend to fluctuate when measured in the short term (3-6 months), a longer period (≥12 months) may be needed to confirm the progression. Assessment of cognitive function is also important for evaluating secondary progression. Compartmentalization of inflammation within the central nervous system is an important reason behind the limited success of disease-modifying therapies (DMTs) for treating SPMS. Most of the DMTs fail to cross the blood-brain barrier; only 38% of the tested DMTs achieved their primary endpoint in SPMS. In Europe, siponimod is the first oral treatment for adults with active SPMS. Particularly, in Central and Eastern Europe, patients with SPMS are still being prescribed less efficacious DMTs and interferons. The absence of alternative treatments in SPMS supports the use of new products (siponimod and others); however the decision to initiate siponimod therapy in more severe patients (EDSS score of 7 or higher) should be individualized in consultation with the payers. The focus should be on early treatment initiation to delay disease progression.

摘要

继发进展型多发性硬化症(SPMS)是一种使人衰弱的疾病,其特征是在最初的复发病程后逐渐恶化。尽管我们对该疾病的认识最近有所进展,但在常规临床实践中,SPMS的诊断和治疗仍然具有挑战性。这篇综述文章的目的是介绍多发性硬化症领域的权威专家对SPMS诊断和管理挑战的看法以及中东欧临床医生的观点。本文还提供了多发性硬化症专家关于改善SPMS诊断和管理状况的建议。中东欧的许多国家多发性硬化症患病率很高(每10万人中超过100例)。与全球趋势一致,在缺乏可靠检测方法或生物标志物的情况下,早期SPMS仍未得到诊断。由于诊断存在不确定性且缺乏普遍接受的疾病定义,临床医生更多地依赖对临床症状的回顾性分析来确诊。由于对SPMS发病时间缺乏认识和了解不足,临床医生可能倾向于关注复发而非进展症状,这导致对SPMS的低估。尽管已经确定了几种进展为SPMS的预测因素,但其预测价值差异很大。因此,将过渡期定义为多发性硬化症的一个单独阶段至关重要。根据专家意见,建议对患者进行频繁随访并定期评估进展情况,以便及时识别从复发缓解型多发性硬化症(RRMS)转变为SPMS的患者。MSProDiscuss工具就是一种用于识别从RRMS进展为SPMS患者的快速评估工具的示例。MS进展通常通过扩展残疾状态量表(EDSS)评分的变化来评估。由于短期内(3 - 6个月)测量时EDSS评分往往会波动,可能需要更长时间(≥12个月)来确认进展情况。评估认知功能对于评估继发进展也很重要。中枢神经系统内炎症的分隔是疾病修饰疗法(DMTs)治疗SPMS效果有限的一个重要原因。大多数DMTs无法穿过血脑屏障;在SPMS中,只有38%的受试DMTs达到了其主要终点。在欧洲,西尼莫德是首个用于治疗成人活动性SPMS的口服药物。特别是在中东欧,仍在为SPMS患者开具疗效较差的DMTs和干扰素。SPMS中缺乏替代治疗方法支持使用新产品(西尼莫德等);然而,对于病情更严重(EDSS评分为7或更高)的患者启动西尼莫德治疗的决定应与医保支付方协商后个体化制定。重点应放在尽早开始治疗以延缓疾病进展上。

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