Bone marrow stem cell therapy safe for acute stroke

Posted on Monday, March 19th, 2012

Sean Savitz, M.D.

Sean Savitz, M.D.

Using a patient’s own bone marrow stem cells to treat acute stroke is feasible and safe, according to the results of a ground-breaking Phase I trial conducted by Medical School researchers.

The trial was the first ever to harvest an acute stroke patient’s own stem cells from the iliac crest of the leg, separate them, and inject them back into the patient intravenously. The first patient was enrolled in March 2009 at Memorial Hermann-Texas Medical Center. This research, with additional funding from the National Institutes of Health, has been expanded to a larger trial to study safety.

“In order to bring stem cells forward as a potential new treatment for stroke patients, we have to establish safety first, and this study provides the first evidence in addressing that goal,” said Sean Savitz, M.D., principal investigator and associate professor of neurology. “Now we are conducting two other stroke cell therapy studies examining safety and efficacy, one of which can be administered up to 19 days after someone has suffered a stroke.”

The study’s findings were published in a recent issue of the Annals of Neurology. Of the 10 patients enrolled in the study, there were no study-related severe adverse events. Although the study was not intended to address efficacy, the investigators compared the study group with historical control patients, who admitted to the stroke service at Memorial Hermann-TMC before the trial began. In that comparison, the study team found a number of patients who did better compared with controls. However, Dr. Savitz says that type of analysis has limitations.

Stroke occurs when blood flow to the brain is interrupted by a blockage or a rupture in an artery, depriving brain tissue of oxygen. It is the third-leading cause of death behind heart disease and cancer and a leading cause of disability. According to the American Stroke Association, nearly 800,000 Americans suffer a stroke each year—one every 40 seconds. The only current treatment for ischemic stroke, the most prevalent kind, is the clot-buster tPA. But only one-third of patients respond well to tPA, so researchers continue to look at other therapies.

Dr. Savitz’s other stem cell studies for stroke are using a regenerative therapy developed by Aldagen that uses a patient’s own bone marrow stem cells injected into the carotid artery; and an umbilical cord-derived cell therapy that can be used “off-the-shelf,” which he said he hopes to bring to community hospitals so that a larger number of stroke patients in Houston have access to ground-breaking research testing new potential therapies.

The Stroke Team at UTHealth and Memorial Hermann-TMC was part of the original group of investigators who studied tPA. It is now researching Doppler ultrasound, endovascular treatment, neuroprotection (hypothermia), and new clot-busting medications for ischemic stroke. Clinical trials for intracerebral hemorrhage (bleeding stroke) include a commonly used diabetes drug shown in preclinical trials to speed the removal of blood from the brain, the first and only study of its kind in Houston.

The Department of Neurology is part of the National Institutes of Health’s Specialized Programs of Translational Research in Acute Stroke (SPOTRIAS) Network. The network centers perform early phase clinical projects, share data, and promote new approaches to therapy for acute stroke. The network currently includes eight stroke research centers across the country.

Memorial Hermann-TMC, a primary teaching hospital of UTHealth, was the first Primary Stroke Care Center in Houston, and is the only one to offer stem cell research for stroke. Researchers are affiliated with the Mischer Neuroscience Institute at Memorial Hermann.

For more information on stem cell therapies for stroke, call 713.500.7079 or visit the website.

Deborah Mann Lake, Office of Advancement, Media Relations

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