A Multicenter, Randomized, Open-label, Controlled Study of HAIC Combined With Camrelizumab and Apatinib Mesylate for Perioperative Treatment of Resectable Hepatocellular Carcinoma With High-risk Recurrence Factors

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorHenan Cancer Hospital

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

Treatment groups

208 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators