About this trial
This study aims to explore the value of the 'HAIC Apatinib Camrelizumab' triple regimen for perioperative treatment of resectable hepatocellular carcinoma. The study adopts a multicenter, randomized, open-label, controlled design and plans to enroll 208 patients, randomly assigned 1:1 to the experimental group and the control group. The experimental group will receive preoperative HAIC combined with targeted-immunotherapy triple regimen neoadjuvant therapy, followed by radical resection, and continue postoperative adjuvant therapy; the control group will undergo surgery directly. The primary endpoint is EFS, and secondary endpoints include R0 resection rate, pCR, MPR, OS, and 1-year/2-year/3-year EFS rates.
Eligibility criteria
Qualifiers
1: 1. Age 18-80, both male and female are acceptable;
Disqualifiers
1: 1. Merge distant metastases;
Trial design
Treatments tested in this trial
- Camrelizumab (anti-PD-1 inhibitor)
- Apatinib Mesylate Tablets
- FOLFOX-HAIC
- Surgery Alone