About this trial
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 criteria
Qualifiers
Patients who have a strong willingness to preserve the anus and are willing to receive neoadjuvant therapy.
Male or Female aged 18-80.
Patients diagnosed with low rectal cancer within 7 cm from the lower edge of the tumor to the anal verge by pelvic MRI and rectal ultrasound, the clinical stage is cT2-3N0M0.
Histologically confirmed rectal adenocarcinoma; Genetic testing suggests MSI-L or MSS, or tumor biopsy immunohistochemistry reveals pMMR, that is, MSH1, MSH2, MSH6, and PMS2 are all positive.
Disqualifiers
Patients with a previous history of malignant tumors besides rectal cancer.
Patients with distant metastases before enrollment.
Patients with metastatic regional or non-regional lymph nodes are assessed by MRI or CT.
Patients with obstruction, perforation, or bleeding that require emergency surgery.
Trial design
Treatments tested in this trial
- Lymph-node-sparing short-course radiotherapy
- Capecitabine
- PD-1/CTLA-4 inhibitor (Aiparolitoworixureli injection)
Treatment groups
Sponsors and collaborators
Sir Run Run Shaw Hospital
Lead sponsor
Sir Run Run Shaw Hospital, Qingchun Campus, Zhejiang University School of Medicine,
Sponsor institution