TY - JOUR
T1 - A double-blind, randomized, controlled, multicenter study to assess the safety and cardiovascular effects of skeletal myoblast implantation by catheter delivery in patients with chronic heart failure after myocardial infarction
AU - Povsic, Thomas J.
AU - O'Connor, Christopher M.
AU - Henry, Timothy
AU - Taussig, Andrew
AU - Kereiakes, Dean J.
AU - Fortuin, F. David
AU - Niederman, Alan
AU - Schatz, Richard
AU - Spencer IV, Richard
AU - Owens, Douglas
AU - Banks, Missy
AU - Joseph, Diane
AU - Roberts, Rhonda
AU - Alexander, John H.
AU - Sherman, Warren
N1 - Funding Information:
MARVEL-1 was conducted in 6 US centers between October 2007 and September 2008. Follow-up was completed in April 2009. The protocol was approved by the institutional review board of each institution, and all patients provided written informed consent. The MARVEL trial was funded by Bioheart Inc (Sunrise, FL). In addition, Dr Povsic was the recipient of a Duke Pepper Older Americans Independence Center Research Career Development Program in Aging Research (5P30AG028716) Award.
Funding Information:
Funding: The MARVEL-1 trial was supported by Bioheart, Inc.
PY - 2011/10
Y1 - 2011/10
N2 - Background: We sought to determine the safety and preliminary efficacy of transcatheter intramyocardial administration of myoblasts in patients with heart failure (HF). Methods: MARVEL is a randomized placebo-controlled trial of image-guided, catheter-based intramyocardial injection of placebo or myoblasts (400 or 800 million) in patients with class II to IV HF and ejection fraction <35%. Primary end points were frequency of serious adverse events (safety) and changes in 6-minute walk test and Minnesota Living With HF score (efficacy). Of 330 patients intended for enrollment, 23 were randomized (MARVEL-1) before stopping the study for financial reasons. Results: At 6 months, similar numbers of events occurred in each group: 8 (placebo), 7 (low dose), and 8 (high dose), without deaths. Ventricular tachycardia responsive to amiodarone was more frequent in myoblast-treated patients: 1 (placebo), 3 (low dose), and 4 (high dose). A trend toward improvement in functional capacity was noted in myoblast-treated groups (Δ6-minute walk test of -3.6 vs +95.6 vs +85.5 m [placebo vs low dose vs high dose; P =.50]) without significant changes in Minnesota Living With HF scores. Conclusions: In HF patients with chronic postinfarction cardiomyopathy, transcatheter administration of myoblasts in doses of 400 to 800 million cells is feasible and may lead to important clinical benefits. Ventricular tachycardia may be provoked by myoblast injection but appears to be a transient and treatable problem. A large-scale outcome trial of myoblast administration in HF patients with postinfarction cardiomyopathy is feasible and warranted.
AB - Background: We sought to determine the safety and preliminary efficacy of transcatheter intramyocardial administration of myoblasts in patients with heart failure (HF). Methods: MARVEL is a randomized placebo-controlled trial of image-guided, catheter-based intramyocardial injection of placebo or myoblasts (400 or 800 million) in patients with class II to IV HF and ejection fraction <35%. Primary end points were frequency of serious adverse events (safety) and changes in 6-minute walk test and Minnesota Living With HF score (efficacy). Of 330 patients intended for enrollment, 23 were randomized (MARVEL-1) before stopping the study for financial reasons. Results: At 6 months, similar numbers of events occurred in each group: 8 (placebo), 7 (low dose), and 8 (high dose), without deaths. Ventricular tachycardia responsive to amiodarone was more frequent in myoblast-treated patients: 1 (placebo), 3 (low dose), and 4 (high dose). A trend toward improvement in functional capacity was noted in myoblast-treated groups (Δ6-minute walk test of -3.6 vs +95.6 vs +85.5 m [placebo vs low dose vs high dose; P =.50]) without significant changes in Minnesota Living With HF scores. Conclusions: In HF patients with chronic postinfarction cardiomyopathy, transcatheter administration of myoblasts in doses of 400 to 800 million cells is feasible and may lead to important clinical benefits. Ventricular tachycardia may be provoked by myoblast injection but appears to be a transient and treatable problem. A large-scale outcome trial of myoblast administration in HF patients with postinfarction cardiomyopathy is feasible and warranted.
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U2 - 10.1016/j.ahj.2011.07.020
DO - 10.1016/j.ahj.2011.07.020
M3 - Article
C2 - 21982657
AN - SCOPUS:80053654714
SN - 0002-8703
VL - 162
SP - 654-662.e1
JO - American heart journal
JF - American heart journal
IS - 4
ER -