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Clinical Trials/NCT01906632
NCT01906632
Completed
Not Applicable

Gene Expression Profiling of Malignant Tumor Predict the Therapeutic Response of DC-CIK Immunotherapy

Capital Medical University1 site in 1 country50 target enrollmentMay 2013
ConditionsMalignant Tumor

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malignant Tumor
Sponsor
Capital Medical University
Enrollment
50
Locations
1
Primary Endpoint
T-Cell Receptor/B-Cell Receptor gene expression
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

To investigate gene expression profile and immunological associated analysis relating to immunotherapy response of patients with malignant tumor after DC-CIK immunotherapy.

Detailed Description

1. The patients with malignant tumor are treated with dendritic cells (DC) plus cytokine induced killer cells (CIK) . 2. Venous blood (4 ml) is collected from each subject and placed into tubes containing Ethylene Diamine Tetraacetic Acid(EDTA) before and after each treatment. Lymphocytes are sorted by Fluorescence Activated Cell Sorting(FACS) and stored at -80°C until processing. 3. The T-Cell Receptor/B-Cell Receptor gene expression is detected by micro-array。 4. Estimate Immunotherapy response, time to disease progression, survival rates and clinical benefit response on patients. Response is assessed using Response Evaluation Criteria in Solid Tumor Group (RECIST) guidelines. Degree of response is used to divide the cancers into two groups: sensitive and non-sensitive to immunotherapy. 5. Compare the gene expression profile between different immunotherapy response groups to explore the mechanism that predict the DC-CIK immunotherapy response.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
June 30, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Capital Medical University
Responsible Party
Principal Investigator
Principal Investigator

Jun Ren MD, PhD

Director, Capita Medical University Cancer Center

Capital Medical University

Eligibility Criteria

Inclusion Criteria

  • histologically confirmed with malignant tumor;
  • Age: 18-80 years;
  • an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;
  • At least one measurable lesion according to the RECIST criteria;
  • Adequate bone marrow, cardiac, liver, and renal function;
  • Life expectancy ≥2 months;
  • Not received other anti-tumor treatment
  • Informed consent signed

Exclusion Criteria

  • previous history of other malignancies;
  • Uncontrolled central nervous system metastases;
  • Serious or uncontrolled concurrent medical illness.

Outcomes

Primary Outcomes

T-Cell Receptor/B-Cell Receptor gene expression

Time Frame: 3 month

Study Sites (1)

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