Key result
Intravenous allogeneic mesenchymal stem cells show similar safety to placebo after acute MI.
Why the study?
Does intravenous allogeneic human mesenchymal stem cells (hMSCs) improve safety and efficacy outcomes in reperfused myocardial infarction patients?
RCT (n=53)
Double-blind
Randomized
Does intravenous allogeneic human mesenchymal stem cells (hMSCs) improve safety and efficacy outcomes in reperfused myocardial infarction patients?
Intravenous allogeneic human mesenchymal stem cells appear safe and may offer provisional efficacy benefits such as reduced ventricular tachycardia and improved ejection fraction in patients after acute myocardial infarction.
Our aim was to investigate the safety and efficacy of intravenous allogeneic human mesenchymal stem cells (hMSCs) in patients with myocardial infarction (MI). Bone marrow-derived hMSCs may ameliorate consequences of MI, and have the advantages of preparation ease, allogeneic use due to immunoprivilege, capacity to home to injured tissue, and extensive pre-clinical support. We performed a double-blind, placebo-controlled, dose-ranging (0.5, 1.6, and 5 million cells/kg) safety trial of intravenous allogeneic hMSCs (Prochymal, Osiris Therapeutics, Inc., Baltimore, Maryland) in reperfused MI patients (n = 53). The primary end point was incidence of treatment-emergent adverse events within 6 months. Ejection fraction and left ventricular volumes determined by echocardiography and magnetic resonance imaging were exploratory efficacy end points. Adverse event rates were similar between the hMSC-treated (5.3 per patient) and placebo-treated (7.0 per patient) groups, and renal, hepatic, and hematologic laboratory indexes were not different. Ambulatory electrocardiogram monitoring demonstrated reduced ventricular tachycardia episodes (p = 0.025), and pulmonary function testing demonstrated improved forced expiratory volume in 1 s (p = 0.003) in the hMSC-treated patients. Global symptom score in all patients (p = 0.027) and ejection fraction in the important subset of anterior MI patients were both significantly better in hMSCs versus placebo subjects. In the cardiac magnetic resonance imaging substudy, hMSC treatment, but not placebo, increased left ventricular ejection fraction and led to reverse remodeling. Intravenous allogeneic hMSCs are safe in patients after acute MI. This trial provides pivotal safety and provisional efficacy data for an allogeneic bone marrow-derived stem cell in post-infarction patients. (Safety Study of Adult Mesenchymal Stem Cells [MSC]
No takes yet. Share an insight, caveat, or question.
Hare et al. (2009) conducted an RCT in acute myocardial infarction (n=53). Intravenous allogeneic human mesenchymal stem cells (Prochymal) vs. Placebo was evaluated on incidence of treatment-emergent adverse events within 6 months. Intravenous allogeneic human mesenchymal stem cells were safe in patients after acute MI, with similar adverse event rates compared to placebo (5.3 vs 7.0 events per patient).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: