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

被引:16
|
作者
Wang, S. Keisin [1 ]
Green, Linden A. [1 ]
Motaganahalli, Raghu L. [1 ]
Wilson, Michael G. [2 ]
Fajardo, Andres [1 ]
Murphy, Michael P. [1 ]
机构
[1] Indiana Univ Sch Med, Div Vasc Surg, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Div Clin Pharmacol, Indianapolis, IN 46202 USA
关键词
QUALITY-OF-LIFE; ENDOTHELIAL PROGENITOR CELLS; SYSTEMATIC REVIEWS; MONONUCLEAR-CELLS; TRANSPLANTATION; IMPLANTATION; NEOVASCULARIZATION; REVASCULARIZATION; ANGIOGENESIS; INJECTION;
D O I
10.1016/j.jvs.2017.01.054
中图分类号
R61 [外科手术学];
学科分类号
摘要
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.
引用
收藏
页码:1850 / 1857
页数:8
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