Cell therapy may mend damaged hearts, study says

April 4, 2016, University of Utah Health Sciences
3-D electrochemical mapping was used to target ixmyelocel-T cell therapy to damaged areas of hearts in patients with end-stage heart failure. Credit: Matthew Brobeck

End-stage heart failure patients treated with stem cells harvested from their own bone marrow experienced 37 percent fewer cardiac events - including deaths and hospital admissions related to heart failure - than a placebo-controlled group, reports a new study. Results from ixCELL-DCM, the largest cell therapy trial for treating heart failure to date, will be presented at the 2016 American College of Cardiology annual meeting and published online in The Lancet on April 4.

"For the last 15 years everyone has been talking about cell therapy and what it can do. These results suggest that it really works," says lead author and cardiac surgeon Amit N. Patel, M.D., M.S., director of Cardiovascular Regenerative Medicine at the University of Utah School of Medicine. He chaired the trial steering committee and led investigations at University of Utah Health Care, a leading enroller in the 31-site, phase 2b clinical trial. The study lays the groundwork for testing in larger trials.

IxCELL-DCM randomly assigned cell therapy or placebo to 126 patients with end-stage ischemic . A small amount of was drawn from each patient and two types of , and M2 macrophages, were selected and expanded in the laboratory. The cell types were chosen because preclinical studies suggested they have the ability to remodel the heart, increase heart tissue, and impact inflammation. The multicellular therapy, called ixmyelocel-T, was then injected into the heart using a minimally invasive procedure. A 3-dimensional electrochemical technique mapped damaged areas in the heart, and cells were delivered directly to them via catheter. On average, the procedure took less than two hours, and if there were no complications, patients were typically discharged the next day.

Cell therapy may mend damaged hearts, study says
Amit N. Patel, M.D., M.S., director of Cardiovascular RegenerativeMedicine at the University of Utah School of Medicine and cardiac surgeonat University of Utah Health Care (right). Credit: University of Utah Health Care

Assessments at 1, 3, 6, and 12 months after treatment showed that cell therapy patients had fewer side effects and complications than the placebo group. At one year, all cardiac events were catalogued, including deaths, and heart-related hospitalizations and unplanned clinic visits.

The double-blind trial found that the group treated with cell therapy had fewer deaths compared to the placebo group (8 vs. 4) and fewer heart failure related hospitalizations (42 of 51 vs. 30 of 58, or 82.4 percent vs. 51.7 percent with a p-value of 0.01), contributing to a 37 percent overall reduction in . Any effects beyond one year remain unknown. The study also reported that there were no, or only very small, statistically significant differences in measures of heart function including performance in an exercise tolerance test, ejection fraction, left ventricular end diastolic volume, and left ventricular end systolic volume. A larger sample size may discern other differences between patients who receive treatment and those who do not.

"This is the first trial of cell therapy showing that it can have a meaningful impact on the lives of patients with heart failure," says Patel. Other cell therapy trials tested single stem cell populations and did not report impacts on the end results of death or other heart related clinical outcomes.

A phase 3 clinical trial will be needed to determine whether ixmyelocel-T can one day be offered as an alternative to current treatments for end-stage heart failure, including heart transplantation and left ventricular assist device therapy.

Explore further: Gene transfer shows promise for treating heart failure

More information: "Ixmyelocel-T for the Treatment of Patients with Ischemic Heart Failure: A Prospective Randomized Double Blind Trial" will be presented at the 2016 American College of Cardiology annual meeting and published in The Lancet on April 4.

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