首页> 外文期刊>Journal of Translational Medicine >Intra-articular injection of two different doses of autologous bone marrow mesenchymal stem cells versus hyaluronic acid in the treatment of knee osteoarthritis: multicenter randomized controlled clinical trial (phase I/II)
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Intra-articular injection of two different doses of autologous bone marrow mesenchymal stem cells versus hyaluronic acid in the treatment of knee osteoarthritis: multicenter randomized controlled clinical trial (phase I/II)

机译:两种不同剂量的自体骨髓间充质干细胞与透明质酸的关节腔内注射治疗膝部骨关节炎:多中心随机对照临床试验(I / II期)

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Background Mesenchymal stromal cells are a promising option to treat knee osteoarthritis. Their safety and usefulness must be confirmed and the optimal dose established. We tested increasing doses of bone marrow mesenchymal stromal cells (BM-MSCs) in combination with hyaluronic acid in a randomized clinical trial. Materials A phase I/II multicenter randomized clinical trial with active control was conducted. Thirty patients diagnosed with knee OA were randomly assigned to intraarticularly administered hyaluronic acid alone (control), or together with 10?×?106 or 100?×?106 cultured autologous BM-MSCs, and followed up for 12?months. Pain and function were assessed using VAS and WOMAC and by measuring the knee motion range. X-ray and magnetic resonance imaging analyses were performed to analyze joint damage. Results No adverse effects were reported after BM-MSC administration or during follow-up. BM-MSC-administered patients improved according to VAS during all follow-up evaluations and median value (IQR) for control, low-dose and high-dose groups change from 5 (3, 7), 7 (5, 8) and 6 (4, 8) to 4 (3, 5), 2 (1, 3) and 2 (0,4) respectively at 12?months (low-dose vs control group p?=?0.005 and high-dose vs control group p?Conclusions The single intraarticular injection of in vitro expanded autologous BM-MSCs together with HA is a safe and feasible procedure that results in a clinical and functional improvement of knee OA, especially when 100?×?106 cells are administered. These results pave the way for a future phase III clinical trial. Clinical Trials.gov identifier NCT02123368. No EudraCT: 2009-017624-72
机译:背景间充质基质细胞是治疗膝骨关节炎的一种有前途的选择。必须确认其安全性和有效性,并确定最佳剂量。在一项随机临床试验中,我们测试了与透明质酸联合使用的骨髓间充质基质细胞(BM-MSC)剂量的增加。材料进行了具有主动控制的I / II期多中心随机临床试验。将30例确诊为膝骨关节炎的患者随机分配到关节腔内单独给予透明质酸(对照),或与10?×?10 6 或100?×?10 6 一起进行关节内给药自体骨髓间充质干细胞,随访12个月。使用VAS和WOMAC并通过测量膝盖运动范围来评估疼痛和功能。进行X射线和磁共振成像分析以分析关节损伤。结果BM-MSC给药后或随访期间均未见不良反应。在所有的随访评估中,BM-MSC管理的患者均根据VAS有所改善,对照组,低剂量和高剂量组的中位数(IQR)从5(3,7),7(5,8)和6变为在12个月时分别为(4,8)至4(3,5),2(1、3)和2(0,4)(低剂量vs对照组p?= 0.005和大剂量vs对照组结论:单次关节腔内体外扩增自体BM-MSC与HA一起注射是一种安全可行的方法,可导致膝OA的临床和功能改善,尤其是当100?×?10 6 给予细胞,这些结果为将来的III期临床试验铺平了道路临床Trials.gov标识符NCT02123368。No EudraCT:2009-017624-72

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