跳至主要内容
临床试验/NCT02215837
NCT02215837Unknown2 期

Randomized,Controlled,Multicenter Study of Autologous Tumor Lysate-pulsed Dendritic and Cytokine-induced Killer Cells(Ag-D-CIK) Combined With Chemotherapy for Gastric Cancer.

Shenzhen Hornetcorn Bio-technology Company, LTD2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2014年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
40
试验地点
2
主要终点
Progress-free survival

研究概览

简要总结

The purpose of this study is to evaluate the safety and efficacy of chemotherapy combined with autologous tumor Lysate-pulsed dendritic with cytokine-induced killer cell (Ag-D-CIK) for gastric cancer.

详细描述

40 patients with stage Ⅰ~Ⅲ Gastric Cancer,who had received surgery and kept their tumor tissue,will be randomly divided into group A(receive Ag-D-CIK treatment and chemotherapy) or group B(just receive chemotherapy),and the randomize ratio will be 1:1. Patients in group A will receive 3 cycles of Ag-D-CIK treatment (every 1 months) and 4 cycles of chemotherapy (every 2 weeks).Patients in group B will receive only 4 cycles chemotherapy(every 2 weeks).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
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

入选标准

  • Patients who can accept curative operations
  • 18~80 years old
  • Histologically confirmed with gastric cancer at stage Ⅰ~Ⅲ
  • Patients who can accept radical gastrectomy;
  • Eastern Cooperative Oncology Group (ECOG) performance status was 0 - 1.

排除标准

  • Hemoglobin<8.0 g/dL,White blood cell <3 x 10^9/L;Platelet count <75 x 10^9/L; ALT, AST, BUN and Cr more than normal limits on 3.0 times
  • Known or suspected allergy to the investigational agent or any agent given in association with this trial
  • Pregnant or lactating patients
  • Known history of Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV) or TreponemaPallidun (TP) infection
  • Patients who are suffering from serious autoimmune disease
  • Patients who had used long time or are using immunosuppressant
  • Patients who had active infection
  • Patients who are suffering from serious organ dysfunction
  • Patients who are suffering from other cancer
  • Other situations that the researchers considered unsuitable for this study.

研究组 & 干预措施

Chemotherapy

Sham Comparator

After accepting chemotherapy according to NCCN guidelines, patients will just regularly follow up.

干预措施: Chemotherapy (Drug)

Ag-D-CIK

Experimental

After accepting chemotherapy according to NCCN guidelines,patients will receive 3 cycles of autologous tumor lysate pulsed D-CIK treatment.

干预措施: Chemotherapy (Drug)

Ag-D-CIK

Experimental

After accepting chemotherapy according to NCCN guidelines,patients will receive 3 cycles of autologous tumor lysate pulsed D-CIK treatment.

干预措施: Ag-D-CIK (Biological)

结局指标

主要结局

Progress-free survival

时间窗: 3 years

次要结局

  • Overall survival(3 years)
  • Quality of life (QOL)(3 years)
  • Phenotypic analysis of T cells(1 years)
  • Severity of adverse events(1 years)

研究者

发起方
Shenzhen Hornetcorn Bio-technology Company, LTD
申办方类型
Industry
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验