HCC - Hepatocellular Carcinoma
Conditions
Brief summary
The goal of this clinical trial is to evaluate the efficacy and safety of combining endovascular denervation (EDN) with transarterial chemoembolization/ hepatic arterial infusion chemotherapy (TACE/HAIC) plus second-line immune-targeted therapy in patients with locally advanced hepatocellular carcinoma (HCC) who have progressed after first-line systemic therapy and present with portal vein tumor thrombus (PVTT). The main questions this study aims to answer are: Does the addition of EDN to standard TACE/HAIC and immune-targeted therapy improve intrahepatic progression-free survival (hPFS) based on RECIST 1.1 criteria? What is the safety profile of the combined treatment, including device-related adverse events? Researchers will compare the experimental group (EDN + TACE/HAIC + immune-targeted therapy) with the control group (TACE/HAIC + immune-targeted therapy alone) in a 1:1 randomized design. A total of 62 participants will be enrolled across 8 centers, with an expected enrollment period of 12 months and a 12-month follow-up period. Participants will: Undergo screening assessments including imaging (CT/MRI), blood tests, and ECG within specified time windows. Receive assigned interventions (EDN procedure or control) during the baseline visit (Day 0). Attend follow-up visits at 1 month (±7 days), 3 months (±14 days), 6 months (±30 days), 9 months (±30 days), and 12 months (±30 days) for repeated imaging, laboratory tests, and safety evaluations. Have their tumor response, survival outcomes, and adverse events monitored throughout the study.
Interventions
COMBINATION_PRODUCTEDN combined with TACE/HAIC and Immuno-Targeted Therapy
Experimental Intervention (Treatment Group): This arm evaluates a novel combination strategy. Participants will undergo a single session of Endovascular Denervation (EDN) in conjunction with standard care. The complete intervention includes: Endovascular Denervation (EDN): A one-time, catheter-based percutaneous procedure for the ablation of peri-arterial sympathetic nerves surrounding the common hepatic artery and/or proper hepatic artery. The procedure utilizes a multi-electrode radiofrequency ablation system (e.g., Netrod®). Ablation parameters are set to 60°C for 120 seconds per site, with a minimum of 20 ablations performed to ensure adequate denervation. On-demand Transarterial Intervention: Following EDN, participants will receive either Transarterial Chemoembolization (TACE) or Hepatic Arterial Infusion Chemotherapy (HAIC), as determined by the treating investigator based on individual patient anatomy and tumor characteristics.
COMBINATION_PRODUCTTACE/HAIC plus Immuno-Targeted Therapy
This is the active comparator intervention representing the current standard-of-care regimen for the study population. Participants randomized to the control group will receive a combination of locoregional and systemic therapy, specifically excluding the experimental Endovascular Denervation (EDN) procedure.
Sponsors
Zhongda Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Aged 18 to 75 years (inclusive), regardless of gender. 2. Diagnosis of CNLC Stage IIIa HCC with portal vein tumor thrombus (vp type 1-3) confirmed by histopathology, cytology, or imaging. 3. Progression of disease after first-line systemic therapy. 4. At least one measurable lesion according to RECIST 1.1 criteria. 5. Child-Pugh class A or B. 6. ECOG performance status of 0 to 2. 7. Scheduled to undergo TACE or HAIC treatment. 8. Adequate hematological, hepatic, and renal function within 14 days prior to study initiation, defined as: White blood cell count ≥2.0×10⁹/L AND neutrophil count ≥1.0×10⁹/L. Platelet count ≥60×10⁹/L. Hemoglobin concentration ≥90 g/L. Total bilirubin ≤2.0 × upper limit of normal (ULN). Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤5 × ULN. Albumin ≥2.8 g/dL. International normalized ratio (INR) ≤1.6. Creatinine ≤1.5 × ULN AND calculated creatinine clearance ≥30 mL/min.
Exclusion criteria
1. Preoperative abdominal CT or MR enhanced scan suggests celiac trunk anatomy is unsuitable for EDN procedure. 2. History of orthostatic hypotension. 3. Diffuse liver tumors or extensive extrahepatic metastases with an expected survival of \<3 months. 4. Cachexia or multi-organ failure. 5. Severe hepatic dysfunction (Child-Pugh class C). 6. Uncorrectable coagulation dysfunction. 7. Presence of severe concurrent infection. 8. Accompanied by Vp4 type portal vein tumor thrombus. 9. Abnormal blood supply to the target lesion that precludes transarterial interventional therapy. 10. History of bilioenteric anastomosis within the past year. 11. Severe allergy to known contrast agents or embolization materials. 12. Pregnant or lactating women, or individuals with childbearing potential planning pregnancy during the trial period. 13. Clinically significant (e.g., active) cardiovascular disease, including: Unstable angina within ≤6 months prior to randomization. New York Heart Association (NYHA) class ≥II congestive heart failure. Poorly controlled arrhythmia despite medication (patients with controlled atrial fibrillation are eligible), or any clinically significant abnormality found on resting ECG. ≥Grade 3 peripheral vascular disease (e.g., symptomatic and interfering with activities of daily living, requiring intervention). Transient ischemic attack or subarachnoid hemorrhage within 6 months prior to randomization, or participation in other drug or device clinical trials within 3 months. 14. History of other malignancies within the past 5 years or concurrent other malignancies. 15. Any other condition deemed by the investigator as unsuitable for participation in this study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| hPFS | From date of randomization until the date of first documented intrahepatic progression or date of death from any cause, whichever comes first, assessed up to 12 months. | Intrahepatic Progression-Free Survival (hPFS) assessed by RECIST 1.1 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| OS | From date of randomization until date of death from any cause, assessed up to 12 months. | Overall Survival (OS) |
| PFS | From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months. | Progression-Free Survival (PFS) assessed by RECIST 1.1 |
| ORR | From date of randomization until the first documented objective response (CR or PR), assessed up to 12 months. | Objective Response Rate (ORR) assessed by RECIST 1.1 |
| MAE | From the time of the baseline procedure (ablation surgery) through 30 days post-procedure | Incidence of Device-Related Composite Major Adverse Events (MAE) |
| SAEs | From date of randomization until the end of study visit at 12 months. | Incidence of All Adverse Events (AEs) and Serious Adverse Events (SAEs) |
| DCR | From date of randomization until the first documented objective response (CR or PR) or stable disease (SD), assessed up to 12 months. | Disease Control Rate (DCR) assessed by RECIST 1.1 |
Countries
China
Contacts
Primary ContactTao Pan
Outcome results
None listed