RecruitingPhase 2Phase 3NCT06644937

Single-arm Clinical Trial of TACE in Combination With Icaritin as Adjuvant Therapy After Surgery in Patients With Hepatocellular Carcinoma at High Risk of Recurrence


Sponsor

Zhujiang Hospital

Enrollment

30 participants

Start Date

Nov 29, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding icaritin (an herbal-derived compound) after TACE (a liver-directed procedure that delivers chemotherapy directly to liver tumors) helps prevent liver cancer from coming back in patients who have had surgery to remove their tumor but are at high risk of recurrence. **You may be eligible if...** - You are between 18 and 75 years old - You have been diagnosed with hepatocellular carcinoma (liver cancer) confirmed by biopsy - You had a complete surgical removal of your tumor (R0 resection) 4–8 weeks ago - You have high-risk features for recurrence, such as a large tumor (≥5 cm), multiple tumors, blood vessel invasion, or low-grade differentiation - You have good liver function (Child-Pugh score 5–6) and good performance status **You may NOT be eligible if...** - Your tumor is a rare subtype (sarcomatoid, fibrolamellar, or mixed liver-bile duct cancer) - You have had another cancer in the past 5 years - You have significant heart, brain, lung, or kidney problems - There is evidence that your cancer has already come back before enrollment - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTACE combined with Acoradine

Transcatheter hepatic arterial chemoembolization (TACE) : the treatment interval was 28 days, the window period was ± 7 days. Subjects received a maximum of 4 TACE treatments; reduced and delayed treatment: laboratory tests were performed before the start of each cycle of TACE, with investigator criteria confirming whether TACE treatment was feasible. Acoradine: 6 tablets bid, taken after meals for 6 months or until intolerable or progressive disease (starting one month after surgery) .


Locations(1)

Zhujiang Hospital, Southern Medical University

Guangzhou, Guangdong, China

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NCT06644937


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