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临床试验/NCT03588442
NCT03588442Unknown不适用

Prospective Surveillance for Very Early Hepatocellular Carcinoma (PRECAR): an Observational Cohort Trial

Eastern Hepatobiliary Surgery Hospital13 个研究点 分布在 1 个国家目标入组 10,000 人开始时间: 2018年7月15日最近更新:
适应症

试验速览

阶段
不适用
入组人数
10,000
试验地点
13
主要终点
Hepatocellular carcinoma

研究概览

简要总结

Hepatocellular carcinoma is one the leading cause of increasing cancer-specific mortality worldwide. Early diagnosis of hepatocellular carcinoma provides opportunity for curative therapeutic approaches and relatively favorable prognosis. Herein, we intended to establish a biosignature for early diagnosis of hepatocellular carcinoma and stratification of risk population for intensive follow-up by implementing biannual follow-up investigation and collecting peripheral blood samples for screening.

详细描述

Patients will be recruited for 1 year and be follow-up for 3 years. Patients will make active hospital visit for collection of blood samples, which will be analyzed to develop a biosignature at the end of the study to detect very early hepatocellular carcinoma and stratify risk population for intensive follow-up.

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
30 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • [1] Cirrhosis cohort
  • Age within 30 to 75 years.
  • Diagnosis of liver cirrhosis within recent 6 months.
  • Liver biopsy: Metavir score of 4 or Ishak score of 5 to
  • No liver biopsy: Presence of ascites, hepatic encephalopathy, or variceal hemorrhage.
  • Satisfying equal to or more than 2 of below conditions.
  • Imaging studies indicating characteristics of liver cirrhosis: irregular liver surface, liver parenchyma particles or nodules, intraperitoneal collateral circulation, or varicose veins with or without splenomegaly (more than 4 cm or 5 ribs).
  • Platelet count < 200 x 10^9/L.
  • Alanine aminotransferase < 5 folds of normal level and liver hardness > 12 kPa.
  • Gastroesophageal varices from endoscopy or imaging studies.
  • [2] HBV infection cohort
  • Age within 40 to 70 years
  • Chronic HBV infection (seropositive for HBsAg over 6 months).

排除标准

  • Cirrhosis cohort
  • (1) Child-Pugh score of C.
  • (2) Hereditary metabolic liver diseases.
  • (3) Presence of HIV-Ab.
  • (4) Previous diagnosis of active pulmonary tuberculosis.
  • (5) Diagnosis of malignant tumors before or during hospitalization, including but not limited to hepatocellular carcinoma.
  • (6) Patients who had received allogeneic blood transfusion or cell therapy within 1 year.
  • (7) Pregnant women.
  • [2] HBV infection cohort
  • (1) Autoimmune liver diseases.
  • (2) Hereditary metabolic liver diseases.
  • (3) Other chronic liver diseases, such as flukes.
  • (4) Presence of HCV, HDV, HEV, or HIV infection.
  • (5) Previous diagnosis of active pulmonary tuberculosis.
  • (6) Diagnosis of malignant tumors before or during hospitalization, including but not limited to hepatocellular carcinoma.
  • (7) Patients who had received allogeneic blood transfusion or cell therapy within 1 year.
  • (8) Pregnant women.

结局指标

主要结局

Hepatocellular carcinoma

时间窗: July 2018 to July 2022

Development of hepatocellular carcinoma

Liver-related disease progression

时间窗: July 2018 to July 2022

HBV and cirrhosis progression

Overall survival

时间窗: July 2018 to July 2022

Death

次要结局

  • Non-hepatocellular carcinoma malignant neoplasm(July 2018 to July 2022)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lei Chen, PhD

Professor

Eastern Hepatobiliary Surgery Hospital

研究点 (13)

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