Colorectal Cancer Clinical Trial
Official title:
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
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.
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.
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