Expanded Activated Lymphocytes (EAL) as Adjuvant Therapy in Patients With HCC at High Risk of Recurrence After Radical Resection
Study Details
Study Description
Brief Summary
This is a multi-center, randomized, open-label pivotal phase II study to evaluate the efficacy and safety of EAL as adjuvant therapy in preventing recurrence in patients with primary HCC at high recurrence risk after radical resection.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Phase 2 |
Detailed Description
HCC, accounting for 80% of all liver cancers, is the third most common cause of cancer-related death worldwide. Radical resection is considered as a curative strategy for patients with primary HCC. However, over 50% of patients experience recurrence after resection, resulting in a very low 5-year survival rate. EAL are ex vivo expanded and activated lymphocytes comprising mainly CD8+ T cells derived from patients' peripheral blood. This is a multi-center, randomized, open-label pivotal phase II study to evaluate the efficacy and safety of EAL in preventing recurrence in patients with primary HCC at high recurrence risk after radical resection. Patients will be randomized in a 1:1 ratio to receive either 20 doses of EAL (1×109~2×1010 per dose) infusion in combination of a single TACE or a single TACE only. Primary endpoint is the independent review committee-determined recurrence-free survival (from randomization to first recurrence or death from any cause). Secondary endpoints include overall survival, cancer-specific survival, adverse events and others.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: EAL Treatment Group The patients with primary HCC will receive 12~20 doses of EAL infusion (1×10^9~2×10^10 cells per dose) in combination of a single transarterial chemoembolization (TACE) after radical resection. |
Biological: Expanded Activated Lymphocytes (EAL)
12~20 doses of EAL (1×10^9~2×10^10 cells per dose) will be infused into patients.
Procedure: transarterial chemoembolization (TACE)
After angiography, fluorouracil will be injected into the proper hepatic artery or the segment of liver where the original lesion is located, and then microcatheter will be introduced into the segment of liver artery where the incision margin is located, and iodized oil injection and epirubicin will be mixed and embolized.
|
| Active Comparator: Control Group The patients with primary HCC will receive a single TACE after radical resection. |
Procedure: transarterial chemoembolization (TACE)
After angiography, fluorouracil will be injected into the proper hepatic artery or the segment of liver where the original lesion is located, and then microcatheter will be introduced into the segment of liver artery where the incision margin is located, and iodized oil injection and epirubicin will be mixed and embolized.
|
Outcome Measures
Primary Outcome Measures
- Recurrence-free survival (RFS) [6 years]
The time from randomization to first documented of disease recurrence determined by IRC or death from any cause (whichever occurs first).
Secondary Outcome Measures
- Overall survival (OS) [6 years]
The time from randomization to death from any cause.
- Cancer-specific survival (CSS) [6 years]
The time from randomization to death from HCC.
- Adverse events (AE) [6 years]
Percentage of participants with adverse events.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Patients with Stage Ia~IIIa primary HCC with high recurrence risk (defined as single tumor ≥5cm in diameter, or single tumor <5cm in diameter with MVI, PVTT, hepatic vein invasion, satellite lesions or AFP ≥400ng/mL, or multiple tumors).
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Patients who have undergone a radical resection.
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ECOG PS Score 0~2.
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Child-Pugh Score ≤ 7.
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Patients with adequate hematologic and end-organ function.
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HBV-HCC and HCV-HCC patients with active viral infection may receive antiviral treatment simultaneously.
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Patients who have a life expectancy of at least 6 months.
Exclusion Criteria:
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Patients with a history of immune deficiency or autoimmune diseases (such as rheumatoid joint disease, systemic lupus erythematosus, vasculitis, multiple sclerosis, insulin-dependent diabetes mellitus, etc.).
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Patients with a history of other malignant tumors in the past 5 years.
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Patients who received chemotherapy, radiotherapy, molecular targeted therapy, biological immunotherapy, and hormone therapy within 1 month prior to screening.
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Patients who have received microwave ablation, cryotherapy, high-power ultrasound focused ablation and other local ablation methods for liver tumors.
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Patients with postoperative organ dysfunction or heart and lung diseases.
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Patients allergic to albumin or with serious allergy history or mental disease.
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Pregnant or lactating women.
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Anticipated other clinical trials within 4 weeks before this trial.
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Patients with HIV or Treponema pallidum infection, septicemia and other uncontrolled infection.
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Patients after organ or bone marrow transplant.
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Patients with drug or alcohol abuse/addiction.
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Any condition that would, in the investigator's judgment, make it unsuitable for the donors to be enrolled.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Chinese PLA General Hospital | Beijing | Beijing | China | 100853 |
Sponsors and Collaborators
- Chinese PLA General Hospital
- Immunotech Applied Science Ltd.
Investigators
- Principal Investigator: Shichun Lu, MD, PhD, Chinese PLA General Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- EAL-HCC-001