About this trial
The primary objective of the study is to screen multi-omics markers in blood samples and construct a prediction model for CRC based on liquid biopsy, and we will further optimize the prediction model by validating its clinical performance externally.
Eligibility criteria
Qualifiers
Aged over 18 years.
Participants confirmed with colorectal adenocarcinoma or advanced adenoma through colonoscopy and pathological examination.
Provision of informed consent prior to any study specific procedures, sampling, and analyses.
No history of colorectal adenomas or sessile serrated polyps.
Disqualifiers
History of other malignant tumors (excluding non-melanoma skin cancer).
Prior or related treatments previously (including colorectal cancer or advanced adenoma surgery, endoscopic treatment, chemotherapy, targeted therapy, immunotherapy, radiation, neoadjuvant therapy, etc.).
Patients with hereditary colorectal diseases (including Lynch syndrome, familial CRC type X (FCCX), familial adenomatous polyposis (FAP), MUTHY-associated polyposis (MAP), Peutz-Jeghers syndrome (PJS), juvenile polyposis syndrome (JPS), serrated polyposis syndrome (SPS), etc.).
Usage of anti-tumor drugs such as methotrexate, cyclophosphamide, mercaptopurine, and bendamustine for other diseases within 30 days before blood collection.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Zhejiang University
Lead sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Sponsor institution
New Horizon Health Technology Co., Ltd
Collaborator