Tislelizumab or Tislelizumab Combined With Lenvatinib Neo-adjuvant Treatment for Resectable RHCC
Launched by SUN YAT-SEN UNIVERSITY · Oct 28, 2020
Trial Information
Current as of July 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at the use of two treatments, Tislelizumab alone or combined with Lenvatinib, for patients who have recurrent hepatocellular carcinoma (a type of liver cancer) and can still undergo surgery. The goal is to see how effective and safe these treatments are before surgery, which is called neoadjuvant treatment. The trial is currently recruiting participants aged 65 to 74, but they also welcome younger patients. To qualify, participants must have been diagnosed with this type of liver cancer after previous treatment, have at least one measurable tumor, and agree to provide some samples for testing.
If you or someone you know is considering joining this trial, participants will undergo regular assessments to monitor their health and the effectiveness of the treatments. However, there are some important factors to consider: individuals who have received certain previous treatments, have cancer spread beyond the liver, or have specific health conditions may not be eligible. This trial provides an opportunity to explore new treatment options that could improve outcomes for patients facing recurrent liver cancer.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Diagnosed as recurrent hepatocellular carcinoma after curative treatment;
- • 2. The criteria for resectability is met;
- • 3. Has at least one evaluable lesion according to the RECIST 1.1 standard and has not received local treatment;
- • 4. Eastern Cooperative Oncology Group score 0-1, Child-pugh score 5-7;
- • 5. Agree to biopsy and blood sample collection;
- • 6. Adequate organ and marrow function.
- Exclusion Criteria:
- • 1. Previously received any transarterial chemoembolization and immune therapy and other local or systemic liver cancer treatments, except for curative ablation;
- • 2. Extrahepatic metastasis;
- • 3. History of gastroesophageal varices or active cardia ulcers associated with a high risk of bleeding;
- • 4. History of autoimmune disease or need to take immunosuppressant drugs for a long time;
- • 5. History of testing positive for human immunodeficiency virus (HIV) or known acquired immunodeficiency syndrome (AIDS);
- • 6. Abnormal organ function
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
Guangzhou, Guangdong, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Similar Trials