Liver Cancer Clinical Trial
Official title:
A Controlled Clinic Trial to Survey the Outcome of Immunotherapy Using Precision T Cells Specific to Multiple Common Tumor-Associated Antigen in Treating Patients Underwent Radical Surgery for Hepatocellular Carcinoma
Objectives:
The purpose of this study is to evaluate the safety and efficacy of radical surgery combined
with dendritic cell-precision multiple antigen T cells in reducing the recurrence and
metastasis of liver cancer
Methods:
This study designs a novel therapy using dendritic cell-precision multiple antigen T cells.
60 postoperative patients of hepatocellular carcinoma will be enrolled. They are randomly
divided into postoperative routine therapy group and dendritic cell-precision multiple
antigen T cells combined with postoperative routine therapy group. Dendritic cell-precision
multiple antigen T cells treatments will be performed every 3 weeks with a total of three
periods. The mail clinical indicators are Progression-Free-Survival and Overall Survival.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | September 2017 |
Est. primary completion date | March 2017 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Age 18~65 years old, male or female 2. Signed informed consent 3. Diagnosis of hepatocellular carcinoma (HCC), radical surgery was performed 4. The recurrence of HCC was not found after the Operation and no other immunotherapy was carried out 5. The Eastern Cooperative Oncology Group (ECOG) score =2 6. Child-Pugh score of liver function = 9 7. Routine blood meets the requirements Exclusion Criteria: 1. Expected Overall survival < 3 months 2. Radical surgery was not performed or recurrence was found after operation 3. Liver function is Childs Pugh C 4. Had received other immunotherapy 5. Other serious diseases:the heart,lung, kidney,digestive, nervous, mental disorders, immune regulatory diseases, metabolic diseases, infectious diseases, etc. 6. Unable or unwilling to provide informed consent, or fail to comply with the test requirements |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
China | Eastern Hepatobiliary Surgery Hospital | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Second Military Medical University |
China,
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* Note: There are 25 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Progress-free survival | 2 years | No | |
Secondary | Overall survival | 2 years | No | |
Secondary | Quality of life | Quality of life core questionnaire will be used. | 2 years | No |
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