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临床试验/NCT04730388
NCT04730388Unknown不适用

Evaluation of the Efficacy and Tolerance of the Association ATEZOLIZUMAB - BEVACIZUMAB in the Treatment of a Locally Advanced Hepatocellular Carcinoma Inoperable or Metastatic in Finistère

University Hospital, Brest0 个研究点目标入组 100 人开始时间: 2021年1月18日最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
主要终点
predictive factor for progression-free survival

研究概览

简要总结

Evaluation of the efficacy and safety of the combination ATEZOLIZUMAB - BEVACIZUMAB in the treatment of locally advanced inoperable or metastatic hepatocellular carcinoma in Finistère

详细描述

Patients treated by ATEZOLIZUMAB and BEVACIZUMAB for an Advanced hepatocellular carcinoma will be followed to observed their safety and the efficacy of this treatment, and to identify prongnosis factors

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • hepatocellular carcinoma locally advanced or metastatic, non able to be resectable, with no prior systemic treatment
  • Child Pugh A and ECOG 0 or 1
  • upper digestiuve endoscopy less than 6 months, if esophageal varcices : must be treated
  • non eligible to receive a locoregional therpay or progressive after this kinf of treatment
  • with informed consent

排除标准

  • refuse to participate
  • under legal protection
  • exclusion criteria from the tempory utilisation authorization

结局指标

主要结局

predictive factor for progression-free survival

时间窗: 12 months

progression-free survival = time between treatment initiation and rediologic or clinical progression

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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