About this trial
The goal of this interventional study is to compare treatment response between transarterial chemoembolization (TACE) combined with lenvatinib and lenvatinib monotherapy in patients with unresectable hepatocellular carcinoma. The study aims to determine whether the addition of TACE to lenvatinib results in improved tumor response compared with lenvatinib alone in a real-world clinical setting.
Eligibility criteria
Qualifiers
Age 18-75 years,
Hepatocellular carcinoma, confirmed by dynamic CT scan / MRI or histopathology, consistent with early (stage A), Intermediate (Stage B), subgroup B, and Advanced (stage C) according to BCLC criteria 2022, without a history of any previous treatment,
At least one measurable lesion based on mRECIST criteria,
ECOG performance status 0-2,
Disqualifiers
Diffuse bi-lobar or multi nodular HCC (more than 10 nodules) with more than equal 50% liver involvement,
Hepatocellular carcinoma with main trunk portal vein thrombosis,
Child Turcotte Pugh Score 10 ( C) or more,
ALBI grade 3,
Trial design
Treatments tested in this trial
- TACE (transarterial chemoembolization) combined with targeted therapy (Lenvatinib)
- Lenvatinib