Clinical trial · Interventional
Efficacy of Sequential TACE and PVE on the Resectability of Hepatitis B Related HCC
Efficacy of Sequential Arterial and Portal Vein Embolizations on Increasing the Resectability of Hepatitis B Related Primary Hepatocellular Carcinoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
A primary hepatocellular carcinoma (HCC) is generally regarded as unresectable if the future liver remnant (FLR)≤40% of total liver volume in patient with underlying liver disease, such as hepatitis B. In China, TACE is the most common treatment for these unresectable HCC. Recently, PVE has been employed to enlarge the FLR of the patients so as to increase the resectability and surgical safety of major hepatectomies. In order to shut the arterio-portal shunt in the liver and control the tumor progress TACE sometimes is performed before PVE. In this study we design a randomized control trial to investigate the efficacy of sequential TACE and PVE on increasing the resectability of hepatitis B related HCC compared with TACE alone.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PVE | Procedure | — | UNRESOLVED |
| TACE | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- TACE
- description
- perform TACE only
- interventionNames
- Procedure: TACE
- type
- EXPERIMENTAL
- label
- TACE+PVE
- description
- perform TACE and PVE sequentially
- interventionNames
- Procedure: TACE
- Procedure: PVE
Primary outcomes (1)
- measure
- the rate of tumor resection after intervention
- timeFrame
- 1 to 2 months
Secondary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. age:20-65years old; 2. with a clinical diagnosis of primary liver cancer, with HBsAg positive,without any therapy for tumor; 3. single lesion with a diameter \>6.5cm,or multiple lesions locating within half liver or adjacent three lobe; 4. estimated liver remnant volume ≤40% 5. with a liver function of Child-Pugh class A,and ALT≤80IU/l. Exclusion criteria: 1. reject to attend; 2. portal vein trunk has been compressed by tumor; 3. diffuse type cancer or with extensive cancer thrombus in main branches of PV,HV,IVC or bile duct; 4. with extrahepatic metastasis; 5. with obvious portal hypertension (with moderate to severe varix in esophagus and/or gastric fundus, enlarged spleen,WBC\<4×109/L, PLT\<80×109/L) 6. with diabetes 7. allergy to iodine
References
Publications (0)
Data not yet available