首页> 外文期刊>Stem cells translational medicine. >Administration of Adult Human Bone Marrow‐Derived, Cultured, Pooled, Allogeneic Mesenchymal Stromal Cells in Critical Limb Ischemia Due to Buerger’s Disease: Phase II Study Report Suggests Clinical Efficacy
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Administration of Adult Human Bone Marrow‐Derived, Cultured, Pooled, Allogeneic Mesenchymal Stromal Cells in Critical Limb Ischemia Due to Buerger’s Disease: Phase II Study Report Suggests Clinical Efficacy

机译:成年人骨髓来源的,培养的,合并的,同种异体间质基质细胞在因伯格症引起的严重肢体缺血中的应用:II期研究报告表明其临床疗效

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Critical limb ischemia (CLI) due to Buerger’s disease is a major unmet medical need with a high incidence of morbidity. This phase II, prospective, nonrandomized, open‐label, multicentric, dose‐ranging study was conducted to assess the efficacy and safety of i.m. injection of adult human bone marrow‐derived, cultured, pooled, allogeneic mesenchymal stromal cells (BMMSC) in CLI due to Buerger’s disease. Patients were allocated to three groups: 1 and 2 million cells/kg body weight (36 patients each) and standard of care (SOC) (18 patients). BMMSCs were administered as 40–60 injections in the calf muscle and locally, around the ulcer. Most patients were young (age range, 38–42 years) and ex‐smokers, and all patients had at least one ulcer. Both the primary endpoints—reduction in rest pain (0.3 units per month [SE, 0.13]) and healing of ulcers (11% decrease in size per month [SE, 0.05])—were significantly better in the group receiving 2 million cells/kg body weight than in the SOC arm. Improvement in secondary endpoints, such as ankle brachial pressure index (0.03 [SE, 0.01] unit increase per month) and total walking distance (1.03 [SE, 0.02] times higher per month), were also significant in the group receiving 2 million cells/kg as compared with the SOC arm. Adverse events reported were remotely related or unrelated to BMMSCs. In conclusion, i.m. administration of BMMSC at a dose of 2 million cells/kg showed clinical benefit and may be the best regimen in patients with CLI due to Buerger’s disease. However, further randomized controlled trials are required to confirm the most appropriate dose. S tem C ells T ranslational M edicine 2017;6:689–699
机译:由于Buerger病而导致的严重肢体缺血(CLI)是主要的未满足医疗需求,且发病率很高。这项II期前瞻性,非随机,开放标签,多中心,剂量范围研究旨在评估i.m.的有效性和安全性。由于Buerger病,在CLI中注射了成人骨髓衍生,培养,合并的同种异体间充质基质细胞(BMMSC)。将患者分为三组:1和200万个细胞/ kg体重(每组36位患者)和护理标准(SOC)(18位患者)。在小腿肌肉内和溃疡周围局部以40-60次注射的方式给予BMMSC。大多数患者是年轻的(年龄在38-42岁之间)并且是吸烟者,并且所有患者至少有1个溃疡。接受200万个细胞/组的主要终点-减少静息疼痛(每月减少0.3个单位[SE,0.13])和溃疡愈合(每月大小减少11%[SE,0.05])明显更好。 kg体重比SOC手臂重。次要终点的改善,例如踝肱压力指数(每月增加0.03 [SE,0.01]个单位)和总步行距离(每月增加1.03 [SE,0.02]倍),在接受200万细胞的组中也很重要/ kg(与SOC臂相比)。报告的不良事件与BMMSC无关或无关。最后,我BMMSC以200万细胞/ kg的剂量给药显示出临床益处,并且可能是由于Buerger病在CLI患者中的最佳治疗方案。但是,需要进一步的随机对照试验来确定最合适的剂量。系统杂志翻译医学杂志,2017年; 6:689–699

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