About this trial

The purpose of this study is to evaluate the safety and efficacy of hepatic arterial infusion chemotherapy (HAIC) in combination with PD-1 inhibitors and Lenvatinib in patients with intermediate or advanced-stage hepatocellular carcinoma (HCC) after failure of systemic therapy recommended by BCLC.

Eligibility criteria

Qualifiers

Has a diagnosis of HCC confirmed by radiology, histology, or cytology;

Barcelona Clinic Liver Cancer (BCLC) stage C with the presence of portal vein tumor thrombus;

Has received previous systemic therapy recommended for HCC by BCLC, and the systemic therapy failed;

Both PD-1inhibitors and Lenvatinib patients received only include marketed drugs but are not limited to HCC approval;

Disqualifiers

The interval between the failure of systemic therapy and the beginning of combination therapy longer than 3 months;

With other malignant tumors;

Unable to meet criteria of combination timeframe described above.

Trial design

Treatments tested in this trial

  • hepatic artery infusion chemotherapy
  • Lenvatinib + PD-1 monoclonal antibody

Treatment groups

84 Participants
are divided into 1 treatment group

Locations

1
The first hospital of China medical university110000, ShenyangLiaoning, China

Sponsors and collaborators

First Hospital of China Medical University

Lead sponsor