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Radioprotective agents for radiation therapy: future trends
Roberta M Johnke1, Jennifer A Sattler, Ron R Allison
1Department of Radiation Oncology, East Carolina University Brody School of Medicine, Greenville, NC 27834, USA.
Future Oncology (London, England)
|December 20, 2014
Summary
This review explores radioprotective compounds for radiation therapy, focusing on antioxidants and agents targeting cellular repair mechanisms to mitigate radiation injury.
Area of Science:
- Radiation oncology
- Pharmacology
- Cellular biology
Background:
- Amifostine and palifermin are the only FDA-approved radioprotective drugs for radiation therapy.
- Numerous other agents demonstrate therapeutic potential, including antioxidants and novel strategies targeting cellular responses to radiation injury.
Purpose of the Study:
- To review the current literature on radioprotector development.
- To emphasize compounds with proven or potential clinical utility in radiation therapy.
Main Methods:
- Literature review of scientific publications on radioprotective agents.
- Analysis of compounds based on their mechanisms of action (e.g., free radical scavenging, targeting cellular repair).
Main Results:
- Several classes of radioprotectors are under investigation, including superoxide dismutase mimetics, nitroxides, dietary antioxidants, cytokines/growth factors, angiotensin-converting enzyme inhibitors, and apoptotic modulators.
- These agents target either direct cellular damage or the subsequent repair pathways activated by radiation.
Conclusions:
- Radioprotector development is advancing beyond traditional antioxidants to include agents that modulate cellular responses to radiation.
- These newer strategies hold significant promise for mitigating radiation injury in patients undergoing radiation therapy.
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