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临床试验/NCT02853903
NCT02853903已完成2 期

Comparison of Autogenic and Allogenic NK Immunotherapy on the Outcome of Recurrent Solid Tumors

Fuda Cancer Hospital, Guangzhou1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2016年7月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
20
试验地点
1
主要终点
Relief degree of tumors

研究概览

简要总结

The aim of this study is the efficacy of autogenic and allogenic natural killer (NK) immunotherapy on recurrent solid tumors.

详细描述

By enrolling patients with multiple kinds of solid tumor adapted to enrolled criteria, this study will document for the first time the short/long term efficacy of auto/allogenic NK cells.The outcome will be evaluated according to local relief degree, progress free survival (PFS) and overall survival (OS).

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
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •All standard therapies have failed according to NCCN guidelines or the patient refuses standard therapies after cancer recurrence
  • •Body tumor 1-6, the maximum tumor length < 5 cm
  • •KPS ≥ 70, lifespan > 6 months
  • •Platelet count ≥ 80×109/L,white blood cell count ≥ 3×109/L, neutrophil count ≥ 2×109/L, hemoglobin ≥ 80 g/L

排除标准

  • •Patients with cardiac pacemaker
  • •Patients with brain metastasis
  • •Patients with grade 3 hypertension or diabetic complication, severe cardiac and pulmonary dysfunction

研究组 & 干预措施

Allogenic NK immunotherapy

Experimental

In this group, the patients will receive more than 4 times of allogenic NK immunotherapies in 3 months. The check indexes are CT scan and blood tests (including tumor markers, lymphocyte subsets and circulating tumor cell).

干预措施: NK immunotherapy (Biological)

Autogenic NK immunotherapy

Active Comparator

In this group, the patients will receive more than 4 times of autogenic NK immunotherapies in 3 months. The check indexes are CT scan and blood tests (including tumor markers, lymphocyte subsets and circulating tumor cell).

干预措施: NK immunotherapy (Biological)

结局指标

主要结局

Relief degree of tumors

时间窗: 3 months

It will be evaluated by the Response Evaluation Criteria in Solid Tumors(RECIST)

次要结局

  • Progress free survival(PFS)(1 year)
  • Overall survival(OS)(3 years)

研究者

发起方
Fuda Cancer Hospital, Guangzhou
申办方类型
Other
责任方
Sponsor

研究点 (1)

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