Phase I Trial of CEA Specific AAV-DC-CTL Treatment in Stage IV Gastric Cancer
Primary Purpose
Gastric Cancer
Status
Active
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
CTL
Sponsored by
About this trial
This is an interventional treatment trial for Gastric Cancer focused on measuring Dendritic Cells, Cytotoxic T-Lymphocytes, Adeno-Associated Virus
Eligibility Criteria
Inclusion Criteria:
- Any patient, at least 18 yrs old regardless of sex, with a diagnosis of Stage IV Gastric Cancer
- Patients with life expectancy greater than or equal to 6 weeks.
- Patients with a Karnofsky score of greater than or equal to 80.
- serum CEA ≥ 20ng/ml.
- Patient provides consent for all required biopsies.
Exclusion Criteria:
- Patients with severe active infection.
- Patients receiving systemic corticosteroid within 48 hours of CTL infusion.
- Patients with HBV,HCV,HIV infection.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
CEA Specific CTL
Arm Description
Patients receiving CEA-specific CTLs as therapy for Gastric Cancer
Outcomes
Primary Outcome Measures
ELISPOT assays
Enzyme-Linked ImmunoSpot (ELISPOT) assay is used for monitoring CEA specific cellular immune responses in Gastric Cancer
Secondary Outcome Measures
overall survival (OS)
Full Information
NCT ID
NCT02496273
First Posted
July 9, 2015
Last Updated
February 19, 2016
Sponsor
The First People's Hospital of Changzhou
1. Study Identification
Unique Protocol Identification Number
NCT02496273
Brief Title
Phase I Trial of CEA Specific AAV-DC-CTL Treatment in Stage IV Gastric Cancer
Official Title
Phase 1 Study of CEA Specific Cytotoxic T Lymphocytes Induced by Dendritic Cells Infected by Recombinant Adeno-associated Virus With CEA Gene in Stage IV Gastric Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2016
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2016 (undefined)
Primary Completion Date
December 2026 (Anticipated)
Study Completion Date
December 2030 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The First People's Hospital of Changzhou
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the clinical safety and preliminary efficacy of CEA specific cytotoxic T lymphocytes induced by dendritic cells infected by recombinant adeno-associated virus with CEA gene in the treatment of stage IV gastric cancer patients.
Detailed Description
Carcinoembryonic antigen (CEA) describes a set of highly related glycoproteins involved in cell adhesion.CEA is normally produced in gastrointestinal tissue during fetal development, but the production stops before birth. The serum levels are raised in some types of cancer,such as Gastric Cancer.The expression of CEA in these cancers and succedent unfavourable prognosis such as tumor hyperplasia, recurrence make CEA become the desirable therapeutic target.
Cancer immunotherapy is the use of the immune system to treat cancer. Immunotherapies fall into three main groups: cellular, antibody and cytokine.Cellular therapies involve the removal of immune cells from the blood or from a tumor. Immune cells specific for the tumor are activated, cultured and returned to the patient where the immune cells attack the cancer. Cytotoxic T cells and dendritic cells can be used in cell-based immunotherapy.
This study is for patients that have a stage Ⅳ gastric cancer with elevated serum CEA concentration. This research study uses special immune system cells called CEA-specific cytotoxic T lymphocytes , a new experimental therapy.
Blood will be collected from the patient and the CEA-specific CTLs will be made.The cells will be injected by IV into the patient.The investigators will follow the patient from their last infusion,monitor side effects of immunotherapy and learn more about the way the T cells are working in the patient's body.The investigators will use blood samples to see how long the T cells last and to look at the immune response to the patient's response to cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer
Keywords
Dendritic Cells, Cytotoxic T-Lymphocytes, Adeno-Associated Virus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CEA Specific CTL
Arm Type
Experimental
Arm Description
Patients receiving CEA-specific CTLs as therapy for Gastric Cancer
Intervention Type
Biological
Intervention Name(s)
CTL
Other Intervention Name(s)
CEA Specific Cytotoxic T-Lymphocytes
Intervention Description
Mononuclear cells (Dendritic Cell,DC precursor) were isolated from the peripheral blood of gasric cancer by density gradient centrifugation and infected with rAAV/CEA virus.Maturation of the DC was induced by granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-4 (IL-4) and tumor necrosis factor-alpha(TNF-alpha). On day 7, the DCs were collected and mixed with T cells at the ratio of 1 to 20 to induce cytotoxic T lymphocytes (CTL).The cells will be proliferated and infused by intravenous (IV) infusion into the patient.
Primary Outcome Measure Information:
Title
ELISPOT assays
Description
Enzyme-Linked ImmunoSpot (ELISPOT) assay is used for monitoring CEA specific cellular immune responses in Gastric Cancer
Time Frame
1 month
Secondary Outcome Measure Information:
Title
overall survival (OS)
Time Frame
1 month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Any patient, at least 18 yrs old regardless of sex, with a diagnosis of Stage IV Gastric Cancer
Patients with life expectancy greater than or equal to 6 weeks.
Patients with a Karnofsky score of greater than or equal to 80.
serum CEA ≥ 20ng/ml.
Patient provides consent for all required biopsies.
Exclusion Criteria:
Patients with severe active infection.
Patients receiving systemic corticosteroid within 48 hours of CTL infusion.
Patients with HBV,HCV,HIV infection.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wu Changping, M.D
Organizational Affiliation
The First People's Hospital of Changzhou
Official's Role
Study Chair
12. IPD Sharing Statement
Citations:
PubMed Identifier
25691731
Citation
Caruana I, Weber G, Ballard BC, Wood MS, Savoldo B, Dotti G. K562-Derived Whole-Cell Vaccine Enhances Antitumor Responses of CAR-Redirected Virus-Specific Cytotoxic T Lymphocytes In Vivo. Clin Cancer Res. 2015 Jul 1;21(13):2952-62. doi: 10.1158/1078-0432.CCR-14-2998. Epub 2015 Feb 17.
Results Reference
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PubMed Identifier
23650543
Citation
Cui H, Zhang W, Hu W, Liu K, Wang T, Ma N, Liu X, Liu Y, Jiang Y. Recombinant mammaglobin A adenovirus-infected dendritic cells induce mammaglobin A-specific CD8+ cytotoxic T lymphocytes against breast cancer cells in vitro. PLoS One. 2013 May 1;8(5):e63055. doi: 10.1371/journal.pone.0063055. Print 2013.
Results Reference
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PubMed Identifier
23325831
Citation
Martino AT, Basner-Tschakarjan E, Markusic DM, Finn JD, Hinderer C, Zhou S, Ostrov DA, Srivastava A, Ertl HC, Terhorst C, High KA, Mingozzi F, Herzog RW. Engineered AAV vector minimizes in vivo targeting of transduced hepatocytes by capsid-specific CD8+ T cells. Blood. 2013 Mar 21;121(12):2224-33. doi: 10.1182/blood-2012-10-460733. Epub 2013 Jan 16.
Results Reference
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Phase I Trial of CEA Specific AAV-DC-CTL Treatment in Stage IV Gastric Cancer
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