About this trial
To assess 1-year recurrence-free survival (RFS) in patients with hepatocellular carcinoma (HCC) who are at high risk of Inguinal orchiectomy recurrence usingTACE combined with icaritin
Eligibility criteria
Qualifiers
The subjects voluntarily cooperated with the study and signed the informed consent,
Male or female, 18 years old ≤ age ≤75 years old,
The histopathologic diagnosis was hepatocellular carcinoma
R0 resection was performed within 4 to 8 weeks before recruitment (patients who were confirmed to have R0 resection by imaging and pathological examination were excluded from the study group if the residual R1, residual R2 or the margin of resection were not clear)
Disqualifiers
Known sarcomatoid hepatocellular carcinoma/mixed hepatocellular carcinoma-cholangiocarcinoma/fibrolamellar hepatocellular carcinoma;
A history of other malignancies in the past 5 years or at the same time;
Severe functional impairment of other important organs such as heart, brain, lung and kidney;
Patients with a history of immunodeficiency or autoimmune disease;
Trial design
Treatments tested in this trial
- TACE combined with Acoradine