About this trial
This multicenter, randomized, open-label, blinded-endpoint Phase II trial assesses the efficacy and safety of tolecizumab (PCSK9 inhibitor) plus sintilimab/CapeOX chemoimmunotherapy as neoadjuvant treatment for pMMR/MSS locally advanced colon adenocarcinoma (cT3c+). 106 patients are 1:1 randomized to the combination or chemoimmunotherapy alone, with pCR as the primary endpoint.
Eligibility criteria
Qualifiers
Signed the written informed consent form and voluntarily participate in the study.
Disqualifiers
Previous anti-tumor treatment for the current colon cancer. Previous use of PCSK9 inhibitors or PD-1/PD-L1 inhibitors. Active autoimmune diseases or a history of autoimmune diseases. Receiving immunosuppressant or systemic glucocorticoid therapy (except for local low-dose glucocorticoid use).
Trial design
Treatments tested in this trial
- Tolecizumab (PCSK9 Inhibitor)
- Sintilimab
Treatment groups
Sponsors and collaborators
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
Lead sponsor
Southwest Hospital, China
Collaborator
Chongqing Shapingba District People's Hospital
Collaborator