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Adipose Mesenchymal Stromal Cell-Based Therapy for Severe Osteoarthritis of the Knee: A Phase I Dose-Escalation Trial

机译:脂肪间质基质细胞治疗严重的膝关节骨关节炎:I期剂量递增试验

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摘要

Osteoarthritis (OA) is the most widespread musculoskeletal disorder in adults. It leads to cartilage damage associated with subchondral bone changes and synovial inflammation, causing pain and disability. The present study aimed at evaluating the safety of a dose-escalation protocol of intra-articular injected adipose-derived stromal cells (ASCs) in patients with knee OA, as well as clinical efficacy as secondary endpoint. A bicentric, uncontrolled, open phase I clinical trial was conducted in France and Germany with regulatory agency approval for ASC expansion procedure in both countries. From April 2012 to December 2013, 18 consecutive patients with symptomatic and severe knee OA were treated with a single intra-articular injection of autologous ASCs. The study design consisted of three consecutive cohorts (six patients each) with dose escalation: low dose (2 x 10(6) cells), medium dose (10 x 10(6)), and high dose (50 x 10(6)). The primary outcome parameter was safety evaluated by recording adverse events-throughout the trial, and secondary parameters were pain and function subscales of the Western Ontario and McMaster Universities Arthritis Index. After 6 months of follow-up, the procedure was found to be safe, and no serious adverse events were reported. Four patients experienced transient knee joint pain and swelling after local injection. Interestingly, patients treated with low-dose ASCs experienced significant improvements in pain levels and function compared with baseline. Our data suggest that the intraarticular injection of ASCs is a safe therapeutic alternative to treat severe knee OA patients. A placebo-controlled double-blind phase Ilb study is being initiated to assess clinical and structural efficacy.
机译:骨关节炎(OA)是成年人中最普遍的肌肉骨骼疾病。它导致与软骨下骨变化和滑膜炎症相关的软骨损伤,从而引起疼痛和残疾。本研究旨在评估膝OA患者关节内注射脂肪来源的基质细胞(ASCs)的剂量递增方案的安全性以及作为次要终点的临床疗效。在法国和德国进行了一项双中心,不受控制的开放式I期临床试验,监管机构批准了这两个国家的ASC扩展程序。从2012年4月至2013年12月,连续18例有症状和严重膝关节炎的患者接受了一次关节内自体ASC注射治疗。研究设计由三个连续的队列(每个队列六名患者)组成,剂量递增:低剂量(2 x 10(6)个细胞),中等剂量(10 x 10(6))和高剂量(50 x 10(6)) )。主要结果参数是通过记录整个试验过程中的不良事件来评估安全性的,次要参数是西安大略省和麦克马斯特大学关节炎指数的疼痛和功能分量表。随访6个月后,发现该过程是安全的,未报告严重不良事件。四名患者在局部注射后经历了短暂的膝关节疼痛和肿胀。有趣的是,与基线相比,接受小剂量ASC治疗的患者的疼痛水平和功能均有明显改善。我们的数据表明,关节内注射ASC是治疗严重膝OA患者的安全治疗选择。一项安慰剂对照的双盲Ilb研究正在启动,以评估临床和结构疗效。

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