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成人异体骨髓源性、培养、混合间充质基质细胞治疗布-加氏病致肢体严重缺血的临床疗效:Ⅱ期研究报告

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.

机构信息

Stempeutics Research, Bangalore, India.

Department of Vascular Surgery, Sri Jayadeva Institute of Cardiovascular Sciences, Bangalore, India.

出版信息

Stem Cells Transl Med. 2017 Mar;6(3):689-699. doi: 10.5966/sctm.2016-0237. Epub 2016 Oct 5.

Abstract

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. Stem Cells Translational Medicine 2017;6:689-699.

摘要

由于伯格氏病引起的严重肢体缺血(CLI)是一种未满足的重大医疗需求,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. 注射成人骨髓源性、培养的、同种异体间充质基质细胞(BMMSC)在伯格氏病引起的 CLI 中的疗效和安全性。患者分为三组:100 万和 200 万个细胞/公斤体重(每组 36 例)和标准治疗(SOC)(18 例)。BMMSC 以 40-60 次小腿肌肉和溃疡周围局部注射。大多数患者年轻(年龄范围为 38-42 岁)且为前吸烟者,所有患者至少有一个溃疡。主要终点(每月缓解静息痛减少 0.3 个单位[SE,0.13])和溃疡愈合(每月溃疡面积缩小 11%[SE,0.05])在接受 200 万个细胞/公斤体重的组中均明显优于 SOC 组。次要终点(如踝肱压指数[每月增加 0.03[SE,0.01]单位]和总步行距离[每月增加 1.03[SE,0.02]倍])的改善在接受 200 万个细胞/公斤体重的组中也明显优于 SOC 组。报告的不良事件与 BMMSC 治疗相关或不相关。总之,i.m. 给予 200 万个细胞/公斤体重的 BMMSC 显示出临床获益,可能是伯格氏病引起的 CLI 患者的最佳治疗方案。然而,需要进一步的随机对照试验来确认最合适的剂量。《干细胞转化医学》2017;6:689-699.

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