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临床试验/NCT03002831
NCT03002831终止2 期

Autologous Cytokine-induced Killer Cells Combined Chemotherapy in Advanced Pancreatic Cancer: A Prospective, Randomized, Open, Single Center Phase II Study

Henan Cancer Hospital1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2016年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
13
试验地点
1
主要终点
Overall Survival

研究概览

简要总结

The purpose of this study is to determine whether Cytokine induced killer cells combined chemotherapy is more effective in the treatment of advanced Pancreatic Cancer.

详细描述

Pancreatic cancer is a devastating malignant disease with a median survival of 3-6 months and a 5-year survival rate of less than 5%. It is necessary to explore more treatment mode to pancreatic cancer especially advanced stage patients. This study is a prospective, randomized, open, single center phase II study. The investigators try to evaluate the efficacy and safety of this treatment mode.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • No less than 18 years old
  • Karnofsky Performance Status over 60
  • Life expectancy more than three months
  • Pathological diagnosed as pancreatic epithelial cell carcinoma
  • Recurrence after surgery or unresectable
  • No experienced chemotherapy or the interval between the last adjuvant chemotherapy and relapse is at least 6 months
  • Measurable lesions (by CT or MRI)
  • No serious mental disorders
  • Adequate organ and bone marrow functions
  • No other serious and the conflict diseases(such as autoimmune diseases, immunodeficiency, organ transplantation)
  • No other malignant tumor history
  • Informed consent and willing to participate in this study

排除标准

  • Received immunosuppressants or glucocorticoid treatment
  • Uncontrolled severe infection or unhealed wound caused by suppurative inflammation
  • Heart disease, insufficient heart function, II degree heart block or occurred myocardial infarction in 6 months
  • Poor pulmonary functions caused by interstitial lung disease and pulmonary reserve volume under 80% of the expected value
  • Other malignant tumor history
  • Transaminase>2.5ULN or bilirubin>3ULN or creatinine >1.25ULN
  • Pregnant or lactating women
  • Obvious bleeding tendency
  • Participated other clinical trails in 1 month
  • Other unsuitable conditions: HIV infection, intravenous drug abusers, etc

研究组 & 干预措施

Chemotherapy

Active Comparator

Tegafur,Gimeracil and Oteracil Potassium Capsules 40-60mg, bid, po, D1-14, Q3w

干预措施: Tegafur-Gimeracil-Oteracil Potassium (Drug)

CIK combined chemotherapy

Experimental

Autologous Cytokine induced killer cells combined Tegafur, Gimeracil and Oteracil Potassium Capsules. After 2 to 4 days of chemotherapy, about 5×109autologous cytokine induced killer cells are transfused into the vein of the patients in one hour.

干预措施: Cytokine-induced Killer Cells (Biological)

CIK combined chemotherapy

Experimental

Autologous Cytokine induced killer cells combined Tegafur, Gimeracil and Oteracil Potassium Capsules. After 2 to 4 days of chemotherapy, about 5×109autologous cytokine induced killer cells are transfused into the vein of the patients in one hour.

干预措施: Tegafur-Gimeracil-Oteracil Potassium (Drug)

结局指标

主要结局

Overall Survival

时间窗: From the date of randomization to the date of death from any cause up to 36 months

次要结局

  • Progression Free Survival(From the date of randomization to the date of first documented progression up to 24 months)
  • Quality of life assessed by Questionnaire(one year by questionnaire)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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