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

ConditionRectal Cancer
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorSir Run Run Shaw Hospital

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

52 Participants
are divided into 1 treatment group

Sponsors and collaborators

Sir Run Run Shaw Hospital

Lead sponsor

Sir Run Run Shaw Hospital, Qingchun Campus, Zhejiang University School of Medicine,

Sponsor institution