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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.

Phase 2RecruitingUniversity of Colorado, DenverNCT07292298Data as of May 2026

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.

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Extracted 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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