Neoadjuvant Immunotherapy ± Radiotherapy in MSI-H/dMMR Locally Advanced Colorectal Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorFudan University

About this trial

This phase II clinical trial evaluates the efficacy and safety of three neoadjuvant regimens in patients with locally advanced microsatellite instability-high/mismatch repair-deficient (MSI-H/dMMR) colorectal cancer (CRC): 1) Regimen A: Dual immune checkpoint blockade with nivolumab plus ipilimumab. 2) Regimen B: Nivolumab plus radiotherapy. 3) Regimen C: Nivolumab monotherapy. The primary objectives are to determine whether: 1) Dual immune checkpoint blockade (Regimen A) is superior to nivolumab monotherapy (Regimen C); and 2) Immunotherapy plus radiotherapy (Regimen B) is superior to nivolumab monotherapy (Regimen C). Methods: Participants will be randomized in a 1:1:1 ratio to one of the three arms. For patients with resectable tumors, surgical resection will be performed. In patients with low rectal cancer and poor prospects for sphincter preservation, a watch-and-wait (WW) strategy is an option if a clinical complete response (CR) is achieved following neoadjuvant therapy.

Eligibility criteria

Qualifiers

Histopathologically confirmed primary colorectal adenocarcinoma.

Radiographic assessment showed a stage II-III based on AJCC Stage 8th ed.

At least 18 years old.

MSI-H or dMMR.

Disqualifiers

Previously received any antitumor therapy for the disease under study, including surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc.

Pregnancy or breastfeeding women.

History of other malignancies within 5 years.

Serious medical illness, such as severe mental disorders, cardiac disease, uncontrolled infection, etc.

Trial design

Treatments tested in this trial

  • Nivolumab
  • Ipilimumab (1mg/kg)
  • PULSAR
  • Radical surgery
  • Watch & wait

Treatment groups

114 Participants
are divided into 3 treatment groups

Sponsors and collaborators