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Research background and purpose: Patients with advanced colorectal cancer face the dilemma of limited treatment options and poor efficacy in the third line treatment stage. Although regorafenib and immune checkpoint inhibitors bring hope to some patients, the efficacy still faces bottlenecks for the vast majority of microsatellite stable patients who are insensitive to immune monotherapy. This study is based on the multi mechanism synergistic theory of "immune activation+vascular inhibition+targeted killing". It innovatively combines autologous DC-CIK cell immunotherapy, domestic PD-1/CTLA-4 bispecific antibody (aparolitovorelli monoclonal antibody), and multi-target tyrosine kinase inhibitor (regorafenib) to evaluate the efficacy and safety of this triple therapy as a third line treatment for advanced colorectal cancer, and explore its immunological mechanism. Research content and methods: This study is a single arm, open label clinical trial. Plan to enroll advanced colorectal cancer patients who have previously failed second-line standard treatment. All participants will receive the following combination therapy regimen: 1. Epaglitovirizumab: 5.0 mg/kg, intravenous injection, once every 21 days. 2. Regorafenib: 120mg, once daily, orally, 1-21 days, repeated every 28 days. 3. DC-CIK cell therapy: Collect, culture, and transfuse cells during specific cycles. The study will strictly follow the protocol for efficacy evaluation (based on RECIST 1.1 standards) and safety monitoring, and a strict quality control and risk management system will be established. Main evaluation indicators and expected outcomes: * Primary endpoint: Objective response rate and safety. * Secondary endpoints: progression free survival, overall survival, duration of remission, and treatment-related immunological responses. * Expected outcome: This study is expected to provide a promising new comprehensive treatment strategy for chemotherapy resistant advanced colorectal cancer, especially MSS type patients, and break through existing efficacy bottlenecks. The research findings will provide high-level evidence-based medicine for the clinical application of this combined approach and lay the foundation for understanding its synergistic mechanism.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Jinling Hospital
Nanjing, Jiangsu, China
Start Date
November 19, 2025
Primary Completion Date
November 30, 2027
Completion Date
November 30, 2027
Last Updated
January 15, 2026
14
ESTIMATED participants
DC-CIK combined with regorafenib ,Iparomlimab and Tuvonralimab Injection
COMBINATION_PRODUCT
Lead Sponsor
JIANG LONGWEI
NCT04704661
NCT06696768
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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