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临床试验/NCT00911092
NCT00911092已完成4 期

Study of Predictive Proteomic Factors of the Response to Exclusive Concomitant Radiochemotherapy in Oesophageal Cancer

Centre Oscar Lambret12 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2007年10月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
50
试验地点
12
主要终点
Proteomic analysis by Protein-Chip Technology of Ciphergen and mass spectrometry

研究概览

简要总结

The scope of the trial is to predict the early complete clinical response to exclusive concomitant radiochemotherapy in esophageal cancer by the study of the pre- and per- therapeutic proteomic profile.

详细描述

Further informations will be provided by Centre Oscar Lambret.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
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

  • Invasive esophageal carcinoma at any stage (all T, N0 or N1, M0 or M1a), histologically proven
  • Treated by exclusive concomitant radiochemotherapy
  • Written informed consent

排除标准

  • Presence of a second uncontrolled cancer
  • Metastatic carcinoma
  • Metastatic disease, except cervical lymphnodes... (M1a)
  • In situ carcinoma
  • Eso-gastric junction cancer (Siewert II ou III)
  • Inclusion in a clinical trial with an experimental drug during the study and until 15 weeks after the end of radiotherapy)

结局指标

主要结局

Proteomic analysis by Protein-Chip Technology of Ciphergen and mass spectrometry

时间窗: 15 weeks after the end of irradiation

Initial complete clinical response

时间窗: 15 weeks after the end of irradiation

次要结局

  • Prolonged clinical response at one year(One year after the end of irradiation)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (12)

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