OncoMatch/Clinical Trials/NCT07292298
Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates
Is NCT07292298 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies non-drug interventions for rectal adenocarcinoma.
Rectal cancer patients who do not achieve a complete response to standard of care chemotherapy and radiation often require surgical resection as part of curative intent therapy. This study will evaluate whether additional "focal" radiation delivered internally (rectal brachytherapy) can provide complete responses and thus spare the requirement for surgery. The main questions are whether: 1) rectal brachytherapy is safe in this clinical treatment paradigm and if 2) rectal brachytherapy improves organ preservation (no need for surgery). The trial involves an additional MRI pelvis and sigmoidoscopy with marker placement to define high-risk residual disease for radiation planning. Subsequently, 3 outpatient brachytherapy treatments are given on a weekly basis. If a patient achieves a complete response to brachytherapy, standard of care non-operative surveillance visits are conducted with study visits aligned during the first two years following brachytherapy.
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Biomarker criteria
Required: MMR proficient
MMR-proficient low-mid rectal adenocarcinoma
Performance status
ECOG 0–3(Limited self-care)
Prior therapy
Must have received: total neoadjuvant therapy — neoadjuvant
who underwent total neoadjuvant therapy
Must have received: external beam chemoradiation — neoadjuvant
Received conventionally fractionated external beam chemoradiation between 45-56 Gy or short-course external beam radiation prescription of 25 Gy to rectal mucosa, in addition to systemic chemotherapy before or after radiation per National Comprehensive Cancer Network (NCCN) guidelines.
Cannot have received: pelvic radiotherapy
Exception: rectal cancer external beam radiation
Pelvic radiotherapy given prior to rectal cancer external beam radiation
Cannot have received: colorectal surgery with anastomotic site at or near HDR brachytherapy target
Exception: prior local excision is not an exclusion criterion
Prior colorectal surgery in which anastomotic site is at or near HDR brachytherapy target
Cannot have received: external beam chemoradiation >56 Gy or short-course radiation >30 Gy
patients received external beam chemoradiation dose with prescription >56 Gy or short-course radiation to rectal mucosa prescription >30 Gy
Lab requirements
Blood counts
CBC at the time of screening must have platelets>50 10^9/L, Hemoglobin>8 g/dL and Absolute Neutrophil Count > 500 10^9/L
CBC at the time of screening must have platelets>50 10^9/L, Hemoglobin>8 g/dL and Absolute Neutrophil Count > 500 10^9/L
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of Colorado Cancer Center · Aurora, Colorado
- University of Rochester Medical Center · Rochester, New York
- Oregon Health and Sciences University · Portland, Oregon
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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