Jan. 18--A decadelong Mayo Clinic research project on using stem cells to repair
damaged heart tissue has won federal approval for human testing, a step that
could have implications for millions of Americans with heart disease.
The U.S. Food and Drug Administration has approved a multistate clinical trial
of 240 patients with chronic advanced symptomatic heart failure to see if the
new procedure produces a significant improvement in heart function, Mayo
officials announced Friday.
Safety testing in humans, completed earlier in Europe, showed a preliminary 25
percent improvement in cardiac outflow, according to Dr. Andre Terzic, director
of the Mayo Clinic's Center for Regenerative Medicine.
The procedure could be a "paradigm shift" in the treatment of heart disease,
Going forward, he said, treatments won't just focus on easing the symptoms of
heart disease, but rather on curing it.
The process, developed in collaboration with Cardio3 BioSciences of Belgium,
involves harvesting stem cells from a patient's bone marrow in the hip,
directing the cells to become "cardiopoietic" repair cells, then injecting them
back into the heart to do their work.
Mayo researcher Dr. Atta Behfar and other members of Terzic's team isolated
hundreds of proteins involved in the "transcription" process that takes place
when stem cells are converted to heart cells. They identified eight proteins
that were crucial, and used them to convert stem cells into heart cells.
"This is unique in the world," Terzic said.
Dr. Ganesh Raveendran, a cardiologist and co-director of the University of
Minnesota's cardiac cell therapy program, called the Mayo research encouraging,
but advised caution. Raveendran said a variety of small stem cell studies have
shown mixed results, but when the treatments were tested in larger studies, they
showed no beneficial effects. "We need to wait and see," he said.
Results by 2015
For now, 40 hospitals in Europe and Israel are enrolling patients in human
trials to test the Mayo procedure. Enrollments are expected to be completed by
the end of the year, and early results should be available in 2015, according to
Dr. Christian Homsy, CEO of Cardio3 BioSciences.
If things go well, patients in Europe could start being treated with the new
technology by the end of 2016, and perhaps a year later for patients in the
Homsy said more than $110 million has been spent in Europe developing and
testing the process, and that he expects his company to increase its presence in
Rochester to work more closely with Mayo researchers.
"Our collaboration with Mayo has been so productive that we have many, many
opportunities that we'd like to explore," Homsy said.
Mayo researchers are working on similar "regenerative medicine" projects
involving many other ailments, including diabetes, diseases of the liver and
lungs, neurological disorders and orthopedics, Terzic said.
"Cardiovascular disease may be the beginning of a ... a magnificent journey of
addressing various diseases that humankind is confronting, especially with the
aging of the population," he said.
Dan Browning -- 612-673-4493
(c)2014 the Star Tribune (Minneapolis)
Visit the Star Tribune (Minneapolis) at www.startribune.com
Distributed by MCT Information Services