About this trial
To evaluate the efficacy and safety of TACE combined with adebrelimab and bevacizumab transformation in unresectable hepatocellular carcinoma
Eligibility criteria
Qualifiers
Age: 18 ~ 75, both male and female;
Strictly comply with the primary liver cancer diagnosis and treatment standard (2022 edition) clinical diagnosis criteria or primary hepatocellular carcinoma diagnosed by pathological histology or cytology examination, and at least one measurable lesions (according to the RECIST1.1 standard, the spiral CT scan of 10mm or short diameter of 15mm);
Patients without previous systematic treatment and inoperable resection / radical ablation surgery, but who can tolerate TACE;
The CNLC stage is Ⅱa-Ⅲb stage;
Disqualifiers
Pregnant or lactating women;
The pathology is clearly cholangiocytic carcinoma or mixed cell carcinoma;
Diffuse liver cancer;
Patients with autoimmune diseases, organ / hematopoietic stem cell transplantation or other malignant tumors (except for cured basal skin cell carcinoma and cervix carcinoma in situ);
Trial design
Treatments tested in this trial
- TACE with adebrelimab and bevacizumab
Treatment groups
Sponsors and collaborators
The First Affiliated Hospital of Xiamen University
Lead sponsor
Jiangsu HengRui Medicine Co., Ltd.
Collaborator