Safety and Efficiency of γδ T Cell Against Hepatocellular Liver Cancer

NCT ID: NCT02425735

Last Updated: 2016-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-04-30

Study Completion Date

2016-06-30

Brief Summary

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In this study, effects of γδT cells on human hepatocellular liver cancer in combination with tumor reducing surgery, for example cryosurgery going to be investigated.

Detailed Description

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Liver tumor will be removed using tumor reducing surgery such as cryosurgery. PBMC of the patient will be separated from peripheral blood. After making them potential cancer killer γδ T Cell and DC-CIK, they will be infused to the patients as an immunotherapy treatment.

Conditions

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Liver Cancer

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Group A

DC-CIK cells will be used against tumor cells.

Group Type EXPERIMENTAL

DC-CIK cells

Intervention Type BIOLOGICAL

DC-CIK cells will be used against tumor cells.

Group B

γδ T cells will be used against tumor cells.

Group Type EXPERIMENTAL

γδ T cells

Intervention Type BIOLOGICAL

γδ T cells will be used against breast tumor.

Group C

Combination of γδ T cells/ DC-CIK be used against tumor cells.

Group Type EXPERIMENTAL

γδ T/DC-CIK cells

Intervention Type BIOLOGICAL

γδ T/DC-CIK cells will be used against breast tumor.

Interventions

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DC-CIK cells

DC-CIK cells will be used against tumor cells.

Intervention Type BIOLOGICAL

γδ T cells

γδ T cells will be used against breast tumor.

Intervention Type BIOLOGICAL

γδ T/DC-CIK cells

γδ T/DC-CIK cells will be used against breast tumor.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

1. Age:18-75
2. Karnofsky performance status \>50
3. Diagnosis with hepatocellular carcinoma cancer based on histology or the current accepted radiological measures.
4. Classification tumor,nodes,metastasis-classification(TNM) stage: Ⅱ,Ⅲ,Ⅳ
5. Will receive cryosurgery, gd Tcells/ DC-CIK.
6. Life expectancy: Greater than 3 months
7. Ability to understand the study protocol and a willingness to sign a written informed consent document

Exclusion Criteria

1. Patients with other kinds of cancer
2. History of coagulation disorders or anemia
3. Patients with heart disease and diabetes
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Jinan University Guangzhou

OTHER

Sponsor Role collaborator

Fuda Cancer Hospital, Guangzhou

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Biological treatment center in Fuda cancer hospital

Guangzhou, Guangdong, China

Site Status

Countries

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China

References

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Alnaggar M, Xu Y, Li J, He J, Chen J, Li M, Wu Q, Lin L, Liang Y, Wang X, Li J, Hu Y, Chen Y, Xu K, Wu Y, Yin Z. Allogenic Vgamma9Vdelta2 T cell as new potential immunotherapy drug for solid tumor: a case study for cholangiocarcinoma. J Immunother Cancer. 2019 Feb 8;7(1):36. doi: 10.1186/s40425-019-0501-8.

Reference Type DERIVED
PMID: 30736852 (View on PubMed)

Other Identifiers

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Gd T cell and Hepatocellular

Identifier Type: -

Identifier Source: org_study_id

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