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临床试验/NCT03599947
NCT03599947Unknown不适用

A Single-centre, Prospective Trial of the Detection of 5-hydroxymethylcytosine (5-hmC) in Plasma Cell-free DNA for Establishing a Model for the Early Diagnosis of Colorectal Cancer

Fudan University1 个研究点 分布在 1 个国家目标入组 1,400 人开始时间: 2018年7月16日最近更新:
适应症

试验速览

阶段
不适用
入组人数
1,400
试验地点
1
主要终点
Sensitivity and specificity of the model in the diagnosis of colorectal cancer

研究概览

简要总结

In this study, the investigators establish a model for the early diagnosis of colorectal cancer based on detection of 5-hydroxymethylcytosine (5-hmC) in training group and validate the effectiveness of the model using a validation group.

详细描述

Many kinds of cancers are associated with changes in epigenetics, including 5-methylcytosine (5-mC) and 5-hydroxymethylcytosine (5-hmC). This changes may help diagnose cancer. The new detection method for 5-hmC can meet the requirements of liquid biopsy.

The traditional diagnostic methods for colorectal cancer is colonoscopy and pathology which are inconvenient and unpleasant, and sometimes, it is difficult for the very patients to get tissues or get enough tissues. In addition, other screening methods for colorectal cancer,such as guaiac-based fecal occult blood testing and a blood test for methylated SEPT9 DNA, have the shortcomings of relatively low sensitivity and specificity. As a result, it is imperative to find a new detection method for early diagnosis of colorectal cancer with high the advantages of high sensitivity and specificity, minimally invasive and convenient.

The aim of this research study is to establish a model for the early diagnosis of colorectal cancer by the detection of 5-hmC in plasma cell-free DNA. Patients who are diagnosed with colorectal cancer by colonoscopy and pathology and not received any anti-tumor therapy (Arm A) will be eligible for inclusion as well as healthy individuals with normal colonoscopy (Arm B). Then, 5-hmC in plasma cell-free DNA will be detected and compared between the two arms of patients (training group) to establish a model to diagnosis other people (validation group) who may suffer from colorectal cancer.

研究设计

研究类型
Observational
观察模型
Other
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

  • Histologically proven colorectal adenocarcinoma
  • No other malignancies in medical history except adequately treated basocellular carcinoma of the skin or in situ carcinoma of the cervix uteri
  • Eastern cooperative oncology group score 0-2
  • Informed consent
  • Healthy people with normal colonoscopy
  • No other malignancies in medical history except adequately treated basocellular carcinoma of the skin or in situ carcinoma of the cervix uteri
  • Eastern cooperative oncology group score 0-2
  • Informed consent

排除标准

  • Patients received chemoradiotherapy or other anti-tumor therapy before being enrolled
  • Patients and/or family members can not understand and accept this study
  • Familial Adenomatosis Polyposis, Lynch Syndrome, acute inflammatory bowel disease
  • Pregnancy or lactation
  • Unsuitable to take part in the clinical trial judged by doctors
  • Pregnancy or lactation
  • Unsuitable to take part in the clinical trial judged by doctors

结局指标

主要结局

Sensitivity and specificity of the model in the diagnosis of colorectal cancer

时间窗: 6-month

Sensitivity and specificity of the model in the diagnosis of colorectal cancer in training group and validation group

次要结局

未报告次要终点

研究者

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

Xu jianmin

Prof.

Fudan University

研究点 (1)

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