The Comparison of TACE-Lenvatinib With TACE-Lenvatinib-ablation for Intermediate Recurrent Hepatocellular Carcinoma
Launched by SUN YAT-SEN UNIVERSITY · Sep 20, 2024
Trial Information
Current as of July 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new treatment approach for patients with recurrent hepatocellular carcinoma (HCC), which is a type of liver cancer that has come back after initial treatment. The trial compares two treatment options: one group will receive a combination of transarterial chemoembolization (TACE) and a medication called Lenvatinib, while the other group will get the same treatments plus a procedure called ablation, which helps to destroy cancer cells directly. Researchers want to see if adding ablation will improve the outcomes for patients with intermediate-stage recurrent HCC.
To participate in this trial, patients need to be between 18 and 75 years old and have been diagnosed with recurrent HCC that is considered intermediate-stage. This means they have two to three tumors, with at least one being larger than 3 cm, and no more than six tumors total. Patients must also have good liver function and a life expectancy of more than three months. Those who join the trial can expect to receive close monitoring and care throughout the study. It's important to remember that this research is aimed at finding better treatment options for liver cancer, and participation will help contribute to important medical knowledge.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. 18-75 years;
- • 2. RHCC diagnosed by imaging;
- • 3. intermediate-stage RHCC (two to three lesions which at least one was \>3 cm in size or more than three tumors);
- • 4. the tumor number was no more than six, and the maximum tumor diameter was ≤5 cm;
- • 5. absence of extrahepatic metastasis or macrovascular invasion;
- • 6. Child-Pugh class A or B;
- • 7. TACE as initial treatment after tumor recurrence and showed no tumor progression after TACE.
- • 8. life expectance \>3 months;
- Exclusion Criteria:
- • 1. under 18 years or over 75 years of age;
- • 2. primary intermediate-stage HCC;
- • 3. RHCC with more than six tumors, or single RHCC
- • (5) RHCC \>5cm; (6) extrahepatic metastasis; (7) macrovascular tumor thrombus;
About Sun Yat Sen University
Sun Yat-sen University, a prestigious institution located in Guangzhou, China, is dedicated to advancing medical research and healthcare innovations. As a leading clinical trial sponsor, the university leverages its extensive academic resources and collaboration with top-tier medical professionals to conduct rigorous clinical studies. Committed to improving patient outcomes and contributing to global health knowledge, Sun Yat-sen University focuses on a wide range of therapeutic areas, employing cutting-edge methodologies to ensure the integrity and efficacy of its research initiatives. Through its clinical trials, the university aims to foster scientific advancements and enhance the quality of care provided to patients both locally and internationally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Beijing, None Selected, China
Patients applied
Trial Officials
Feng Duan
Study Director
Chinese PLA General Hospital
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported