RecruitingPhase 2NCT07068763

Node-Sparing Short-Course Radiation Combined With Capecitabine and PD-1/CTLA-4 for MSS Early Rectal Cancer

Node-Sparing Short-Course Radiation Combined With Capecitabine and PD-1/CTLA-4 for MSS Early Middle and Low Rectal Cancer (mRCAT-E): An Open-label, Single-arm, Prospective Multicenter Clinical Trial


Sponsor

Sir Run Run Shaw Hospital

Enrollment

52 participants

Start Date

Oct 9, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a single-arm, prospective, multicenter study evaluating a novel neoadjuvant treatment strategy for patients with early, mid-low rectal adenocarcinoma that is microsatellite stable (MSS). Instead of irradiating regional lymph nodes, we deliver short-course radiotherapy (25 Gy in 5 fractions) exclusively to the primary tumor ("lymph-node-sparing" approach), immediately followed by four 3-week cycles of capecitabine plus combined PD-1/CTLA-4 immune checkpoint inhibitors. Two weeks after completing chemo-immunotherapy, tumor response is assessed. Patients who achieve a clinical complete response may enter a "watch-and-wait" program; others will undergo local excision or total mesorectal excision (TME) as appropriate. The primary endpoint is the rate of complete response (clinical and pathological). Secondary endpoints include organ-preservation rate, 3-year local recurrence, 3-year disease-free and overall survival, toxicity, and quality-of-life measures. Results from a pilot study suggest that this regimen may substantially improve complete response rates while reducing radiation-related toxicity, potentially allowing more patients to avoid radical surgery and permanent stoma.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination treatment approach for people with early low rectal cancer who strongly want to preserve their anus and avoid a permanent colostomy — combining short-course radiation, an oral chemotherapy drug (capecitabine), and two immunotherapy drugs — before surgery. **You may be eligible if...** - You are 18 to 80 years old - You have been diagnosed with low rectal adenocarcinoma (cancer within 7 cm of the anus) - Your cancer is early stage (cT2-3N0M0) and classified as MSS or MSI-L (a specific genetic test) - You have not received any prior treatment for this cancer - You strongly wish to preserve bowel function and avoid a permanent stoma **You may NOT be eligible if...** - Your cancer has spread to distant organs or regional lymph nodes - You have had another cancer previously - You need emergency surgery due to obstruction, perforation, or bleeding - You are pregnant, breastfeeding, or have cognitive impairment - You are immune-compromised or have HIV infection Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

RADIATIONLymph-node-sparing short-course radiotherapy

Three-dimensional conformal or intensity-modulated radiotherapy targeting only the primary tumor bed (no regional lymph nodes), delivering a total dose of 25 Gy in 5 Gy fractions over five consecutive days.

DRUGCapecitabine

Oral capecitabine 1,000 mg/m² administered twice daily on Days 1-14 of each 21-day cycle, for a total of four cycles.

DRUGPD-1/CTLA-4 inhibitor (Aiparolitoworixureli injection)

Intravenous PD-1/CTLA-4 bispecific monoclonal antibody at 5 mg/kg every 3 weeks for four cycles, starting on Day 8 after completion of radiotherapy.


Locations(1)

Sir run run shaw hospital

Hangzhou, Zhejiang, China

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NCT07068763


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