Final results of a phase I-II trial using ex vivo expanded autologous Mesenchymal Stromal Cells for the treatment, of osteoarthritis of the knee confirming safety and suggesting cartilage regeneration

被引:131
作者
Soler, Robert [1 ]
Orozco, Lluis [1 ]
Munar, Ana [1 ]
Huguet, Marina [2 ]
Lopez, Ramon [3 ]
Vives, Joaquim [3 ]
Coll, Ruth [3 ]
Codinach, Margarita [3 ]
Garcia-Lopez, Joan [3 ,4 ]
机构
[1] Hosp Quiron Teknon, ITRT, Carrer Vilana 12, Barcelona 08022, Spain
[2] CETIR Clin Pilar, Dept Magnet Resonance Imaging, Carrer Balmes 271, Barcelona 08006, Spain
[3] Banc Sang & Teixits, Div Terapies Avancades XCELIA, Edifici Dr Frederic Duran i Jorda, Barcelona 08005, Spain
[4] Univ Autonoma Barcelona, Chair Transfus Med & Cellular & Tissue Therapies, Campus UAB, Bellaterra 08193, Spain
关键词
Osteoarthritis; Articular cartilage; T2; mapping; Mesenchymal Stromal Cells; STEM-CELLS; ARTICULAR-CARTILAGE; THERAPY; VALIDITY; TRANSPLANTATION; RELIABILITY; DEFECTS; TISSUE; T2;
D O I
10.1016/j.knee.2015.08.013
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Cellular therapies have shown encouraging results in the treatment of chronic osteoarthritis.(OA). Herein, we present the final results of a phase I-II clinical trial assessing the feasibility, safety and efficacy of ex vivo expanded autologous bone marrow Mesenchymal Stromal Cells (MSC, XCEL-M-ALPHA), infused intra-articularly, in patients with knee OA. Methods: Fifteen patients (median age = 52 years) with grade II(9) or III(6) gonarthrosis (Kellgren & Lawrence classification) and chronic pain were treated with an intra-articular infusion of 40.9 x 10(6) +/- 0.4 x 10(6) MSCin a phaseI-IIprospective, open-label, single-dose, single-arm clinical trial. Endpoints were safety and tolerability. Efficacy was measured by the Visual Analogue Scale for pain, algofunctional Health Assessment Questionnaire, Quality of Life (QoL) SF-36 questionnaire, Lequesne functional index and WOMAC score. Cartilage integrity was assessed by Magnetic Resonance Imaging and quantitative T2-mapping at 0, 6 and 12 months. Results: The cell-based product was well tolerated with few reported Adverse Events (mild arthralgia and low back pain). There was a relevant decrease in the intensity of pain since day 8 after the infusion, that was maintained after 12 months. The SF-36 QoL test showed improvement of parameters including bodily pain, role physical and physical functioning at month 12. The health assessment questionnaire revealed a significant decrease of incapacity. Moreover, T2 mapping showed signs of cartilage regeneration in all patients at 12 months post-treatment. Conclusions: Single intra-articular infusion of XCEL-M-ALPHA is a safe and well-tolerated cell-based product, associated with a long-lasting amelioration of pain, improvement of QoL (up to four years), and signs of cartilage repair. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:647 / 654
页数:8
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