The purpose of this study is to evaluate the efficacy and safety of sorafenib combined with hepatic arterial infusion chemotherapy (HAIC) compared with lenvatinib combined with HAIC in patients with advanced hepatocellular carcinoma (HCC)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
250
12 mg (or 8 mg) once daily (QD) oral dosing.
400mg BID daily oral dosing
administration of Oxaliplatin , fluorouracil, and leucovorin via the tumor feeding arteries
Cancer Center Sun Yat-sen University
Guangzhou, Guangdong, China
RECRUITINGOverall survival
Overall survival
Time frame: Time Frame: 12 months
Time to progression
Time to progression
Time frame: Time Frame: 12 months
Adverse Events
Time frame: [Time Frame: 30 days]
Progression Free Survival (PFS)
Time frame: Time Frame: 12 months
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