One-Year Safety Analysis of the COMPARE-AMI Trial: Comparison of Intracoronary Injection of CD133 Bone Marrow Stem Cells to Placebo in Patients after Acute Myocardial Infarction and Left Ventricular Dysfunction.

Bone Marrow Research Pub Date : 2011-01-01 Epub Date: 2011-02-27 DOI:10.1155/2011/385124
Samer Mansour, Denis-Claude Roy, Vincent Bouchard, Louis Mathieu Stevens, Francois Gobeil, Alain Rivard, Guy Leclerc, François Reeves, Nicolas Noiseux
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引用次数: 48

Abstract

Bone marrow stem cell therapy has emerged as a promising approach to improve healing of the infarcted myocardium. Despite initial excitement, recent clinical trials using non-homogenous stem cells preparations showed variable and mixed results. Selected CD133(+) hematopoietic stem cells are candidate cells with high potential. Herein, we report the one-year safety analysis on the initial 20 patients enrolled in the COMPARE-AMI trial, the first double-blind randomized controlled trial comparing the safety, efficacy, and functional effect of intracoronary injection of selected CD133(+) cells to placebo following acute myocardial infarction with persistent left ventricular dysfunction. At one year, there is no protocol-related complication to report such as death, myocardial infarction, stroke, or sustained ventricular arrhythmia. In addition, the left ventricular ejection fraction significantly improved at four months as compared to baseline and remained significantly higher at one year. These data indicate that in the setting of the COMPARE-AMI trial, the intracoronary injection of selected CD133(+) stem cells is secure and feasible in patients with left ventricle dysfunction following acute myocardial infarction.

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为期一年的COMPARE-AMI试验安全性分析:急性心肌梗死和左心室功能障碍患者冠状动脉内注射CD133骨髓干细胞与安慰剂的比较
骨髓干细胞治疗已成为改善梗死心肌愈合的一种有希望的方法。尽管最初令人兴奋,但最近使用非同质干细胞制备的临床试验显示出不同和混合的结果。选择的CD133(+)造血干细胞是具有高潜能的候选细胞。在此,我们报告了最初20名患者的一年安全性分析,该试验是首个双盲随机对照试验,比较急性心肌梗死伴持续性左心室功能障碍后冠状动脉内注射选定的CD133(+)细胞与安慰剂的安全性、有效性和功能效果。一年内,无方案相关并发症报告,如死亡、心肌梗死、中风或持续性室性心律失常。此外,与基线相比,左心室射血分数在4个月时显着改善,并在1年后显着保持较高。这些数据表明,在COMPARE-AMI试验的背景下,在急性心肌梗死后左心室功能障碍患者中冠状动脉内注射选定的CD133(+)干细胞是安全可行的。
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