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Mesenchymal precursor cells as adjunctive therapy in recipients of contemporary left ventricular assist devices.
- Source :
-
Circulation [Circulation] 2014 Jun 03; Vol. 129 (22), pp. 2287-96. Date of Electronic Publication: 2014 Mar 28. - Publication Year :
- 2014
-
Abstract
- Background: Allogeneic mesenchymal precursor cells (MPCs) injected during left ventricular assist device (LVAD) implantation may contribute to myocardial recovery. This trial explores the safety and efficacy of this strategy.<br />Methods and Results: In this multicenter, double-blind, sham-procedure controlled trial, 30 patients were randomized (2:1) to intramyocardial injection of 25 million MPCs or medium during LVAD implantation. The primary safety end point was incidence of infectious myocarditis, myocardial rupture, neoplasm, hypersensitivity reaction, and immune sensitization (90 days after randomization). Key efficacy end points were functional status and ventricular function while temporarily weaned from LVAD support (90 days after randomization). Patients were followed up until transplant or 12 months after randomization, whichever came first. Mean age was 57.4 (±13.6) years, mean left ventricular ejection fraction was 18.1%, and 66.7% were destination therapy LVADs. No safety events were observed. Successful temporary LVAD weaning was achieved in 50% of MPC and 20% of control patients at 90 days (P=0.24); the posterior probability that MPCs increased the likelihood of successful weaning was 93%. At 90 days, 3 deaths (30%) occurred in control patients, and none occurred in MPC patients. Mean left ventricular ejection fraction after successful wean was 24.0% (MPC=10) and 22.5% (control=2; P=0.56). At 12 months, 30% of MPC patients and 40% of control patients were successfully temporarily weaned from LVAD support (P=0.69), and 6 deaths (30%) occurred in MPC patients. Donor-specific HLA sensitization developed in 2 MPC and 3 control patients and resolved by 12 months.<br />Conclusions: In this preliminary trial, administration of MPCs appeared to be safe, and there was a potential signal of efficacy. Future studies will evaluate the potential for higher or additional doses to enhance the ability to wean LVAD recipients off support.<br />Clinical Trial Registration Url: http://www.clinicaltrials.gov. Unique identifier: NCT01442129.<br /> (© 2014 American Heart Association, Inc.)
- Subjects :
- Adult
Aged
Cell- and Tissue-Based Therapy adverse effects
Cell- and Tissue-Based Therapy methods
Double-Blind Method
Female
Heart Neoplasms epidemiology
Humans
Incidence
Male
Mesenchymal Stem Cell Transplantation adverse effects
Middle Aged
Myocarditis epidemiology
Treatment Outcome
Heart Failure therapy
Heart-Assist Devices
Mesenchymal Stem Cell Transplantation methods
Mesenchymal Stem Cells
Ventricular Dysfunction, Left therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1524-4539
- Volume :
- 129
- Issue :
- 22
- Database :
- MEDLINE
- Journal :
- Circulation
- Publication Type :
- Academic Journal
- Accession number :
- 24682346
- Full Text :
- https://doi.org/10.1161/CIRCULATIONAHA.113.007412