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Mesenchymal precursor cells as adjunctive therapy in recipients of contemporary left ventricular assist devices.

Authors :
Ascheim DD
Gelijns AC
Goldstein D
Moye LA
Smedira N
Lee S
Klodell CT
Szady A
Parides MK
Jeffries NO
Skerrett D
Taylor DA
Rame JE
Milano C
Rogers JG
Lynch J
Dewey T
Eichhorn E
Sun B
Feldman D
Simari R
O'Gara PT
Taddei-Peters WC
Miller MA
Naka Y
Bagiella E
Rose EA
Woo YJ
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.)

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