Single Arm, Prospective, Multicenter Clinical Study of TACE With Adebrelimab and Bevacizumab for Unresectable Hepatocellular Carcinoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorThe First Affiliated Hospital of Xiamen University

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

71 Participants
are divided into 1 treatment group

Sponsors and collaborators

The First Affiliated Hospital of Xiamen University

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Collaborator