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Measuring Radiation Toxicity Using Circulating Cell-Free DNA in Prostate Cancer Patients
Natalie A Lockney1, Randal H Henderson1, Steven G Swarts1
1Department of Radiation Oncology, University of Florida College of Medicine, Gainesville and Jacksonville, FL, USA.
International Journal of Particle Therapy
|February 7, 2022
Summary
Cell-free DNA (cfDNA) measured during radiation therapy (RT) for prostate cancer may predict gastrointestinal (GI) toxicity. This preliminary study suggests cfDNA could help identify patients at risk for GI side effects.
Area of Science:
- Oncology
- Radiation Oncology
- Biomarkers
Background:
- Circulating cell-free DNA (cfDNA) rises after radiation therapy (RT) due to tissue damage.
- cfDNA can be measured within hours of RT initiation.
- This study investigated the correlation between cfDNA levels and toxicity in prostate cancer patients undergoing RT.
Purpose of the Study:
- To examine the relationship between cfDNA levels during the first week of RT and early/late gastrointestinal (GI) and genitourinary (GU) toxicity.
- To determine if cfDNA can serve as a predictive biomarker for RT-induced toxicities.
Main Methods:
- Prospective study of 54 patients receiving RT for nonmetastatic prostate cancer.
- Blood samples collected pre-RT and daily during the first week of RT.
- Toxicity assessments (GI and GU) performed at baseline, weekly during RT, and at 6 and 12 months post-RT.
Main Results:
- No grade 3 or higher toxicities were observed.
- Acute and late grade 2 GI toxicity showed significant correlation with pre-RT cfDNA and cfDNA levels during RT.
- Acute and late GU toxicity did not correlate significantly with cfDNA levels.
Conclusions:
- cfDNA levels show potential for predicting GI toxicity in patients undergoing prostate cancer RT.
- cfDNA may offer a biological estimate to complement traditional dose-volume histogram assessments.
- Further multi-institutional studies are underway to validate these findings.

