New drug cuts risk of deadly transplant side effect in half

Tuesday, December 10, 2013

Washington: A new class of drugs reduced the risk of patients contracting a serious and often deadly side effect of lifesaving bone marrow transplant treatments, according to a study from researchers at the University of Michigan Comprehensive Cancer Centre.

Dr Pavan Reddy

Dr Pavan Reddy

The study, the first to test this treatment in people, combined the drug vorinostat with standard medications given after transplant, resulting in 22 per cent of patients developing graft-vs-host disease compared to 42 per cent of patients who typically develop this condition with standard medications alone. Results of the study appear in The Lancet Oncology.

“Graft-vs-host disease is the most serious complication from transplant that limits our ability to offer it more broadly. Current prevention strategies have remained mostly unchanged over the past 20 years. This study has us cautiously excited that there may be a potential new way to prevent this condition,” says lead study author Dr Sung Choi, assistant professor of paediatrics at the U-M Medical School.

Vorinostat is currently approved by the US Food and Drug Administration to treat certain types of cancer. But U-M researchers, led by senior study author Dr Pavan Reddy found in laboratory studies that the drug had anti-inflammatory effects as well — which they hypothesized could be useful in preventing graft-vs-host disease, or GVHD, a condition in which the new donor cells begin attacking other cells in the patient’s body.

The study enrolled 61 older adults from the University of Michigan and Washington University in St Louis who were undergoing a reduced-intensity bone marrow transplant with cells donated from a relative. Patients received standard medication used after a transplant to prevent GVHD. They also received vorinostat, which is given as a pill taken orally. Fifty of the 61 participants completed the full 21-day course of vorinostat.

The researchers found vorinostat was safe and tolerable to give to this vulnerable population, with manageable side effects. In addition, rates of patient death and cancer relapse among the study participants were similar to historical averages.

The results mirror those found in the laboratory using mice. Dr Reddy, the Moshe Talpaz Professor of Oncology and professor of internal medicine at the U-M Medical School, has been studying this approach in the lab for eight years.

“This is an entirely new approach to preventing graft-vs-host disease,” Dr Reddy says. Specifically, vorinostat targets histone deacetylases, which are different from the usual molecules targeted by traditional treatments.

“Vorinostat has a dual effect as an anti-cancer and an anti-inflammatory agent. That’s what’s potentially great about using it to prevent graft-vs-host, because it may also help prevent the leukaemia from returning,” says Dr Reddy, who is also co-director of the haematologic malignancies and bone marrow transplant programme at the U-M Comprehensive Cancer Centre.

“We are encouraged by our findings,” Dr Choi says. “Vorinostat combined with standard graft-vs-host disease prophylaxis after related-donor transplant appears to be safe and associated with lower than expected incidence of acute GVHD. Future studies are needed to assess the effect of vorinostat in broader transplant settings. We are currently investigating vorinostat plus standard therapies to prevent GVHD in transplants with an unrelated donor.”

by Nicole Fawcett

Categories: Medicine, RESEARCH, Transplant Surgery

Tags: , , , , , , , ,

  More from Medicine

Safety concerns linger for generic oncology drugs in developing countries


Pharmaceutical industry-sponsored meals associated with higher prescribing rates


Researchers combine drugs to develop a new treatment for human parainfluenza virus


Common painkillers are more dangerous than we think


Stronger evidence found for link between prenatal exposure to paracetamol and the risk of developing asthma


US scientists document trajectory of Zika virus for first time

Comments »

No comments yet.

Name (required)
E-mail (required - never shown publicly)
URI
Your Comment (smaller size | larger size)
You may use <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong> in your comment.