Clinical trial · Interventional
Autologous Immune Cell Therapy in Primary Hepatocellular Carcinoma Patients Following Resection and TACE Therapy
Clinical Study of the Safety of Autologous Immune Cell Therapy in Primary Hepatocellular Carcinoma Patients Following Resection and TACE Therapy
- 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)
Although liver resection, liver transplantation, a-interferon, Transarterial Chemo Embolization (TACE), percutaneous ethanol injection (PEI), Percutaneous microwave coagulation therapy (PMCT), Radiofrequency ablation (RFA) provide options to treat patients with HCC, the high recurrence rate of mid-late stage liver cancer still exists. The safety of autologous Immune Cell Therapy in Primary Hepatocellular Carcinoma (HCC) Patients Following Resection and TACE Therapy will be evaluated.
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 |
|---|---|---|---|
| Primary Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| DC-TC+GM-CSF | Biological | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- DC-TC+GM-CSF
- interventionNames
- Biological: DC-TC+GM-CSF
Primary outcomes (1)
- measure
- Vital signs,physical examinations and adverse events
- timeFrame
- one year
- description
- The number of adverse events along with the results of vital signs measurements, physical examinations, and clinical laboratory tests will be used to determine the safety profile of DC-TC.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Voluntary written informed consent signed by patient or legal guardian, obtained prior to study enrollment. 2. BCLC Classification A-B 3. Patients who are good surgical candidates for HCC resection 4. ECOG Performance Score, 0-1 5. Child-Pugh Rating, A 6. Expected survival greater than 6 months Exclusion Criteria: 1. History of anaphylactic reaction to GM-CSF 2. Congestive heart failure, unstable angina or other underlying cardiac disease; history of thrombosis currently requiring anticoagulation 3. Mental or psychological illness preventing cooperation with treatment, efficacy evaluations, or unable to understand the informed consent process 4. Primary cancers of any kind or location, other than hepatocellular carcinoma 5. Excluding hepatitis, any active or unresolved infection including HIV, EBV, CMV, RPR, TB, etc. 6. Autoimmune disease requiring therapy; immunodeficiency, or any disease process requiring immunosuppressive therapy. 7. Prior clinical trial requiring patient to receive an investigational drug within two weeks of enrollment. 8. Pregnant or lactating women. 9. Patients with the intention to receive transplantation 10. Significant comorbidity or other active medical condition that could be eminently life threatening in the opinion of the investigator, including no active blood clotting or bleeding diathesis. 11. Evidence of metastatic disease.
References
Publications (0)
Data not yet available