Testing low-dose radiation to treat severe pneumonia for COVID-19
Previous studies have shown that low-dose, whole-lung radiation in the form of X-rays can effectively treat severe pneumonia with minimal side effects. Two clinical trials are applying a modern version of this concept to test patients who have acute respiratory distress syndrome (ARDS) as a result of COVID-19 infection.
For these trials, patients will undergo a single treatment of whole-lung radiation to target and reduce pulmonary inflammation associated with COVID-19 infection in two separate phase II clinical trials. The studies are led by Arnab Chakravarti, MD, chair of the Department of Radiation Oncology at The Ohio State University and member of the Translational Therapeutics Program at Ohio State’s Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC – James).
Some patients diagnosed with COVID-19 pneumonia will experience worsening disease that can become very serious, requiring the use of a ventilator. This is caused by inflammation in the lungs from the virus caused by overreaction of the immune system.
For this study, researchers will give a form of radiation therapy that uses high-energy X-ray beams to target the lungs and reduce inflammation caused by the COVID-19 virus. Usually, it is given at considerably higher doses to treat cancers.
“We believe adding a single treatment of low-dose X-rays to the lungs might reduce the amount of inflammation in the lungs from a COVID-19 infection, which could help a patient to breathe without use of a ventilator,” says Chakravarti.
The first trial — called PREVENT — is a national trial for COVID-19 pneumonic patients who do not yet require mechanical breathing intervention but are experiencing severe respiratory distress. Chakravarti serves as the national principal investigator of this study, which will involve up to 20 additional hospitals across the United States. The second trial, VENTED, is for patients who are critically ill and on a ventilator. This study is also led by Chakravarti and will be conducted exclusively at Ohio State. Treatments will be administered in a COVID-19-only containment area and with a single machine not used for standard oncology care.
Patients will be monitored before and after treatment to better understand the molecular biology behind disease treatment and response. Scientists will use results from this study to determine if there is sufficient evidence of clinical benefit to warrant a substantial phase II randomized clinical trial.
