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Minimal clinically important difference for the 6-min walk test: literature review and application to Morquio A syndrome

机译:6分钟步行测试的最小临床重要差异:文献综述及对Morquio A综合征的应用

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Morquio A syndrome is an ultra-rare, inherited lysosomal storage disorder associated with progressive, multi-systemic clinical impairments, causing gradual loss of functional capacity and endurance, impaired quality of life, and early mortality. Studies in Morquio A patients have used the 6-min walk test (6MWT) to assess functionality and endurance and to evaluate disease progression or efficacy of treatment. The objective of the present study was to review minimal clinically important differences (MCIDs) for the 6MWT reported for disease states that widely use the 6MWT to evaluate clinical benefit and to discuss the results in view of the challenges in estimating MCID for ultra-rare diseases, using the case of elosulfase alfa in Morquio A patients. A systematic literature search was performed using Embase and Medline to identify studies specifically estimating the MCID using either anchor-based or distribution-based methods. A total of 19 publications on 17 studies were identified; none of these included patients with Morquio A syndrome or the wider disease category of lysosomal storage disorders. Therefore, the MCIDs determined by studies in patients with respiratory, cardiovascular, or musculoskeletal disease were compared to changes in the 6MWT seen in Morquio A patients in the pivotal phase 3 clinical trial of elosulfase alfa enzyme replacement therapy. The literature review showed a mean MCID for the 6MWT of 7% change (range 3–15%) in studies using anchor-based methods and a 9% change (range 4–16%) using distribution-based methods. Results of the elosulfase alfa clinical trial and its extension showed a placebo-adjusted 14.9% improvement in the 6MWT from baseline at week 24, which was greater than the mean MCID based on the results of the systematic literature review. After 2?years, 6MWT distance increased by a mean of 20.7% from baseline in a modified per-protocol population, versus a reduction of 6.9% in comparable untreated patients from the MorCAP natural history study over the same period. Although further research is required to establish the MCID of the 6MWT in Morquio A patients, the presented data provide further evidence for the positive effect of elosulfase alfa in this patient population.
机译:Morquio A综合征是一种罕见的遗传性溶酶体贮积病,与进行性多系统临床损害相关,导致功能能力和耐力逐渐丧失,生活质量受损和早期死亡。在Morquio中进行的研究A患者使用了6分钟步行测试(6MWT)来评估功能和耐力,并评估疾病的进展或治疗效果。本研究的目的是审查针对广泛使用6MWT评估临床获益的疾病状态所报告的6MWT的最小临床重要差异(MCID),并鉴于估计超罕见疾病的MCID所面临的挑战,讨论结果,使用在Morquio A患者中使用的elosulfase alfa案例。使用Embase和Medline进行了系统的文献检索,以鉴定使用基于锚点或基于分布的方法专门评估MCID的研究。总共确定了涉及17个研究的19个出版物;这些患者均不包括Morquio A综合征或较广泛的溶酶体贮积病疾病患者。因此,将在呼吸道,心血管或肌肉骨骼疾病患者中进行的研究确定的MCID与elosulfase alfa酶替代治疗的关键性3期临床试验中Morquio A患者的6MWT变化进行了比较。文献综述显示,在使用锚定方法的研究中,6MWT的平均MCID变化为7%(范围3–15%),而在基于分布方法的研究中,平均MCID变化为9%(范围4–16%)。埃洛硫酶α临床试验及其扩展的结果显示,在第24周时,安慰剂调整后的6MWT与基线相比有14.9%的改善,这比系统文献综述的平均MCID还要大。 2年后,经过修改的按协议人群中6MWT距离与基线相比平均增加了20.7%,而同期MorCAP自然病史研究中未治疗的可比患者减少了6.9%。尽管需要进一步的研究以建立Morquio A患者的6MWT的MCID,但本文提供的数据仍提供了进一步的证据证明α-硫磺酶在该患者人群中的积极作用。

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