Role of molecularly-cloned hematopoietic growth factors after acute high-dose radiation exposures.
Hillard M LazarusJames O ArmitageRobert Peter GalePublished in: Journal of radiological protection : official journal of the Society for Radiological Protection (2021)
Therapy of acute, high-dose whole-body exposures of humans to ionizing radiations is a complex medical challenge. Since 1944 more than 400 radiologic accidents have been registered with more than 3000 substantial radiation exposures and 127 fatalities. There are several potential interventions including supportive care, transfusions, preventative or therapeutic anti-infection drugs, molecularly-cloned myeloid growth factors and hematopoietic cell transplants. We discuss the use of the granulocyte and granulocyte-macrophage colony-stimulating factor (G-CSF and GM-CSF) to treat acute high-dose ionizing radiation exposures. Considerable data in experimental models including monkeys indicate use of these drugs accelerates bone marrow recovery and in some but not all instances increases survival. In ten accidents since 1996, 30 victims received G-CSF alone or with other growth factors. Twenty-six victims survived. In seven accidents since 1986, 28 victims received GM-CSF alone or with other growth factors; 18 victims survived. However, absent control or data from randomized trials, it is not possible to know with certainty what role, if any, receiving G-CSF or GM-CSF was of benefit. Given the favorablebenefit-to-riskratio of molecularly-cloned myeloid growth factors, their use soon after exposure to acute, high-dose whole-body ionizing radiations is reasonable.
Keyphrases
- high dose
- bone marrow
- low dose
- liver failure
- stem cell transplantation
- air pollution
- respiratory failure
- drug induced
- radiation induced
- healthcare
- aortic dissection
- cerebrospinal fluid
- mesenchymal stem cells
- acute myeloid leukemia
- electronic health record
- adipose tissue
- physical activity
- peripheral blood
- hepatitis b virus
- single cell
- machine learning
- stem cells
- immune response
- radiation therapy
- intensive care unit
- risk assessment
- quality improvement
- artificial intelligence
- mechanical ventilation
- free survival
- acute respiratory distress syndrome
- chronic pain