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骨髓刺激外周动脉疾病关键肢体缺血治疗垫套件(MOBILE)试验的原理与设计:一项针对关键肢体缺血的自体骨髓细胞疗法的研究

Rationale and design of the MarrowStim PAD Kit for the Treatment of Critical Limb Ischemia in Subjects with Severe Peripheral Arterial Disease (MOBILE) trial investigating autologous bone marrow cell therapy for critical limb ischemia.

作者信息

Wang S Keisin, Green Linden A, Motaganahalli Raghu L, Wilson Michael G, Fajardo Andres, Murphy Michael P

机构信息

Division of Vascular Surgery, Indiana University School of Medicine, Indianapolis, Ind.

Division of Clinical Pharmacology, Indiana University School of Medicine, Indianapolis, Ind.

出版信息

J Vasc Surg. 2017 Jun;65(6):1850-1857.e2. doi: 10.1016/j.jvs.2017.01.054. Epub 2017 Apr 5.

Abstract

OBJECTIVE

Critical limb ischemia (CLI) continues to place a significant encumbrance on patients and the health care system as it progresses to limb loss and long-term disability. Traditional methods of revascularization offer a significant benefit; however, for one-third of CLI patients, these surgical options are not technically possible or patency is severely limited by disease burden (deemed "poor-option" for revascularization). In a previous phase I trial, we demonstrated intramuscular injection of concentrated bone marrow aspirate (cBMA) via MarrowStim (Zimmer Biomet, Warsaw, Ind) harvest is safe and may decrease major amputation in patients with CLI unfit for surgical revascularization. Therefore, we describe and rationalize the MarrowStim PAD Kit for the Treatment of Critical Limb Ischemia in Subjects with Severe Peripheral Arterial Disease (MOBILE) trial, a study geared to provide the pivotal proof of efficacy of cBMA in CLI.

METHODS

MOBILE is a multicenter, randomized, double-blind, placebo-controlled trial designed to assess the efficacy of intramuscular injections of cBMA in promoting amputation-free survival in patients with poor-option CLI. Patients (aged >21 years) with rest pain or tissue loss resulting from advanced peripheral arterial disease, as characterized by ankle-brachial index (<0.6), toe-brachial index (<0.4), or transcutaneous pressure of oxygen (<50 mm Hg), were eligible for inclusion if surgical revascularization was not possible secondary to advanced disease.

RESULTS

Treatment and 1-year follow-up of 152 patients enrolled in MOBILE are completed. Long-term follow-up is ongoing. Currently, we are in the process of unblinding the initial results for preliminary data analysis.

CONCLUSIONS

If successful, MOBILE could add definitive, high-quality evidence in support of cBMA for the treatment of poor-option CLI patients and provide an additional modality for patients who face amputation secondary to advanced limb ischemia.

摘要

目的

严重肢体缺血(CLI)若发展至肢体丧失和长期残疾,会持续给患者及医疗系统带来重大负担。传统的血管重建方法有显著益处;然而,对于三分之一的CLI患者而言,这些手术方案在技术上不可行,或者通畅率因疾病负担而严重受限(被视为血管重建的“不良选择”)。在之前的I期试验中,我们证明了通过MarrowStim(齐默生物科技公司,印第安纳州华沙)采集器进行肌肉注射浓缩骨髓抽吸物(cBMA)是安全的,并且可能减少不适合手术血管重建的CLI患者的大截肢率。因此,我们描述并论证了用于治疗严重外周动脉疾病患者严重肢体缺血的MarrowStim PAD套件(MOBILE)试验,该研究旨在提供cBMA治疗CLI疗效的关键证据。

方法

MOBILE是一项多中心、随机、双盲、安慰剂对照试验,旨在评估肌肉注射cBMA对不良选择CLI患者无截肢生存的疗效。因晚期外周动脉疾病导致静息痛或组织缺失的患者(年龄>21岁),以踝臂指数(<0.6)、趾臂指数(<0.4)或经皮氧分压(<50 mmHg)为特征,若因疾病进展无法进行手术血管重建,则符合纳入标准。

结果

MOBILE试验纳入的152例患者已完成治疗及1年随访。长期随访正在进行。目前,我们正在对初步结果进行揭盲以进行初步数据分析。

结论

如果成功,MOBILE试验可为cBMA治疗不良选择CLI患者提供确凿的高质量证据,并为面临晚期肢体缺血继发截肢的患者提供另一种治疗方式。

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