Adaptive Radiation BOost for Rectal Cancer: a Phase I Dose Escalation Study (ARBOR)
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.
• Subjects must have histologically or cytologically confirmed rectal adenocarcinoma.
• Subjects must have T2-3, N0-1, M0 rectal cancer. Staging will be done by MRI pelvis and CT chest and abdomen with contrast. PET-CT will be an acceptable alternative for the CT chest and abdomen.
• Subjects must be willing to undergo MRI scans.
• Age ≥18 years.
• ECOG performance status 0 or 1.
• Estimated survival of ≥ 12 months.
• Subjects must have normal organ and marrow function as defined below
‣ Absolute neutrophil count \> =1,000/mcL
⁃ Platelets \>= 75,000/mcL
⁃ Total bilirubin \< 3 mg/dL
• Subjects must be able to tolerate the chemotherapy regimens outlined in the treatment plan (Section 5.0), both before and after ART.
‣ Before ART: Capecitabine at a dose of 825 mg/m²
⁃ After ART: FOLFOX combination chemotherapy, or 5-FU, or capecitabine
• Subjects must possess the ability to understand and willingness to sign a written informed consent and HIPAA consent document. Translation services including translation of informed consent documents will be provided, as feasible, to encourage diversity of inclusion of eligible patients.