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临床试验/NCT04340986
NCT04340986招募中不适用

Cohort Study of Patients With Primary Hepatocellular Carcinoma or Cholangiocarcinoma

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 1,250 人开始时间: 2020年9月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
1,250
试验地点
1
主要终点
Overall survival

研究概览

简要总结

The main objective is to describe the evolution of patients treated for a primary malignant hepatobiliary tumor (hepatocellular carcinoma or cholangiocarcinoma) over the long course.

详细描述

The collection of data from patients with CHC and cholangiocarcinomas who are cancers with poor prognosis is a major challenge to improve patients'care (diagnosis, prognosis); facilitate the search for new therapeutic targets and the follow-up of clinical studies; and develop personalized treatments.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria :
  • Age ≥ 18 years olds
  • Medical care in Nephrology department since 2015
  • Cholangiocarcinoma:
  • Histologically and cytologically documented cholangiocarcinoma, regardless of the stage of the disease
  • Hepatocellular carcinoma:
  • Hepatocellular carcinoma at any stage of the disease, presenting the diagnostic criteria according to the diagnostic criteria of Barcelona : Tumor of more than 1 cm, developed on cirrhosis liver with arterial phase hyperenhancement and washout in the portal venous or delayed phases on CT and MRI
  • Hepatocellular histologically documented

排除标准

  • Lack of patient non-opposition

结局指标

主要结局

Overall survival

时间窗: 5 years

Hepatocellular carcinoma and Cholangiocarcinoma : Overall survival is defined as the survival 5 years after the inclusion.

次要结局

  • Disease free survival(2 and 5 years)
  • Overall survival(5 years)
  • Progression time under chemotherapy(Time of progression under chemotherapy up to 5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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