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Study identifier: NCT07221058 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Adaptive Radiation Boost for Rectal Cancer

Condition: Rectum Cancer, Adenocarcinoma  ·  Sponsor: Fox Chase Cancer Center

PhasePhase 1
Planned participants37
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to find out if giving extra adaptive radiation therapy after standard chemoradiation treatment is safe and helpful for people with rectal cancer. The main questions the study aims to answer are: * Can this approach help target the most aggressive cancer cells more accurately, while protecting nearby healthy tissue? * Can it reduce the side effects that people may experience during treatment? Participants will: * First receive standard treatment: radiation (45 Gy in 25 sessions) along with a chemotherapy pill called capecitabine. * Then get extra radiation using MRI scans every two weeks to adjust the treatment based on how the tumor responds. * Use a small balloon during treatment to help aim the radiation and protect healthy areas. * Finally, receive additional chemotherapy (such as FOLFOX) for four months.

This description comes directly from the study's public registry record.

Talk to the study team

Joshua Meyer, MD  ·  215-728-2667  ·  Joshua.Meyer@fccc.edu

Jianli Hu, MD, PhD  ·  267-449-1431  ·  Jianli.Hu@fccc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Fox Chase Cancer CenterPhiladelphia, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07221058