Clinical Study of the Safety of Autologous Immune Cell Therapy in Primary Hepatocellular Carcinoma Patients Following Resection and TACE Therapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 8
- 试验地点
- 1
- 主要终点
- Vital signs，physical examinations and adverse events
研究概览
简要总结
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.
详细描述
The study is a single center,open label trial. To obtain safety information on toxicities and adverse events attributable to the subcutaneous injections of autologous dendritic cells incubated with irradiated autologous tumor stem cells and suspended in GM-CSF in patients with HCC.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Voluntary written informed consent signed by patient or legal guardian, obtained prior to study enrollment.
- •BCLC Classification A-B
- •Patients who are good surgical candidates for HCC resection
- •ECOG Performance Score, 0-1
- •Child-Pugh Rating, A
- •Expected survival greater than 6 months
排除标准
- •History of anaphylactic reaction to GM-CSF
- •Congestive heart failure, unstable angina or other underlying cardiac disease; history of thrombosis currently requiring anticoagulation
- •Mental or psychological illness preventing cooperation with treatment, efficacy evaluations, or unable to understand the informed consent process
- •Primary cancers of any kind or location, other than hepatocellular carcinoma
- •Excluding hepatitis, any active or unresolved infection including HIV, EBV, CMV, RPR, TB, etc.
- •Autoimmune disease requiring therapy; immunodeficiency, or any disease process requiring immunosuppressive therapy.
- •Prior clinical trial requiring patient to receive an investigational drug within two weeks of enrollment.
- •Pregnant or lactating women.
- •Patients with the intention to receive transplantation
- •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.
- •Evidence of metastatic disease.
结局指标
主要结局
Vital signs，physical examinations and adverse events
时间窗: one year
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.
次要结局
未报告次要终点