Tolecizumab Plus Chemoimmunotherapy for pMMR/MSS Locally Advanced Colon Adenocarcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorDaping Hospital and the Research Institute of Surgery of the Third Military Medical University

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

106 Participants
are divided into 2 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