RECOMMEND: Early Screening of Colorectal Cancer Based on Plasma Multi-omics Combining With Artificial Intelligence

Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05587452
Collaborator
Cangzhou Central Hospital (Other), Weifang Medical University (Other), Heji Hospital affiliated to Changzhi Medical College (Other), Beijng Fengtai Hospital (Other)
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Study Details

Study Description

Brief Summary

To evaluate the accuracy and effectiveness of a novel screening method based on plasma multi-omics combining with artificial intelligence in a large prospective cohort for the detection of colorectal cancer and advanced adenomas.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Colonoscopy
  • Diagnostic Test: Test of ctDNA methylation
  • Diagnostic Test: Test of characteristics of ctDNA fragment

Detailed Description

Minimally invasive detection of circulating tumor DNA (ctDNA) in peripheral blood of patients with colorectal malignancies via liquid biopsy has emerged as a promising biomarker. This is urgently needed, as conventional imaging and plasma protein-derived biomarkers lack sensitivity and specificity.The goal of this observational study is to evaluate the effectiveness and accuracy of a novel screening method based on plasma multi-omics combining with artificial intelligence in five hospitals around China for the detection of colorectal cancer and advanced adenomas.

Study Design

Study Type:
Observational
Anticipated Enrollment :
950 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Early Screening of Colorectal Cancer Based on Plasma Multi-omics Combining With Artificial Intelligence-a Multi-center, Prospective Study
Actual Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Healthy group

People without colorectal adenoma or cancer

Diagnostic Test: Colonoscopy
Colonoscopy is performed to identify whether the patient has colorectal adenoma or cancer

Diagnostic Test: Test of ctDNA methylation
A specified panel is used to detect the site of methylation of ctDNA in plasma

Diagnostic Test: Test of characteristics of ctDNA fragment
Low pass whole genome sequencing is used to detect the characteristics of ctDNA fragment

Advanced adenoma group

People with colorectal adenoma

Diagnostic Test: Colonoscopy
Colonoscopy is performed to identify whether the patient has colorectal adenoma or cancer

Diagnostic Test: Test of ctDNA methylation
A specified panel is used to detect the site of methylation of ctDNA in plasma

Diagnostic Test: Test of characteristics of ctDNA fragment
Low pass whole genome sequencing is used to detect the characteristics of ctDNA fragment

Colorectal cancer group

People with colorectal cancer

Diagnostic Test: Colonoscopy
Colonoscopy is performed to identify whether the patient has colorectal adenoma or cancer

Diagnostic Test: Test of ctDNA methylation
A specified panel is used to detect the site of methylation of ctDNA in plasma

Diagnostic Test: Test of characteristics of ctDNA fragment
Low pass whole genome sequencing is used to detect the characteristics of ctDNA fragment

Outcome Measures

Primary Outcome Measures

  1. Sensitivity [Through study completion, an average of 1 year]

    Sensitivity (for colorectal cancer and\or advanced precancerous neoplasm) of this plasm-based multi-omics test. The diagnostic colonoscopy procedure is reference method. Lesions will be confirmed as malignancy or precancerous by pathological biopsy.

  2. Specificity [Through study completion, an average of 1 year]

    Specificity (for colorectal cancer and\or advanced precancerous neoplasm) of this plasm-based multi-omics test. The diagnostic colonoscopy procedure is reference method. Lesions will be confirmed as malignancy or precancerous by pathological biopsy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Inclusion criteria for colorectal cancer/advanced adenoma 1) Voluntarily participate and sign the informed consent form, and be able to cooperate with the entire research process 2) Be able to provide sufficient and qualified blood samples for this study 3) Patients with pathological diagnosis of colorectal cancer stage I-III (TNM staging according to AJCC 8th edition colorectal cancer staging system) 4) No previous cancer treatment, including chemotherapy, radiotherapy, targeted or immunotherapy, and any surgery treat 5) Advanced adenoma should at least meet one of the following conditions: ① Diameter >10mm ② Villus-tubiform adenoma ③ More than 25% of villi structure in mixed adenoma ④High-grade intraepithelial neoplasia

  2. Inclusion criteria for healthy people 1) Voluntarily participate and sign the informed consent form, and be able to cooperate with the entire research process 2) Diagnosed without colorectal adenoma or cancer by colonoscopy within 12 months

Exclusion Criteria:
  1. Exclusion criteria for colorectal cancer/advanced adenoma 1) Women who are pregnant or breastfeeding 2) Currently diagnosed with another cancer or have a history cancer 3) Persistent fever or receiving anti-inflammatory treatment within 14 days before blood samples are taken in this study 4) Receiving blood transfusion within 30 days 5) Receiving organ transplantation or previous non-autologous (allogeneic) bone marrow or stem cell transplantation 6) Digestive tract bleeding, obstruction, perforation and any trauma or surgery within 3 months 7) Poor physical condition, not suitable for extraction blood samples 8) Subjects who are judged by the investigator to be unsuitable to participate in this study for other reasons;

  2. Exclusion criteria for healthy people 1) Women who are pregnant or breastfeeding 2) Receiving organ transplantation or previous non-autologous (allogeneic) bone marrow or stem cell transplantation 3) Have a history cancer 4) Receiving blood transfusion within 30 days 5) Poor physical condition, not suitable for extraction Blood samples

  1. Diagnosed with precancerous lesions by colonoscopy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cancer Hospital Chinese Academy of Medical Sciences Beijing Beijing China 100021
2 Beiijing Fengtai Hospital Beijing Beijing China
3 Cangzhou Central Hospital Cangzhou Hebei China
4 Affiliated Hospital of Weifang Medical University Weifang Shandong China
5 Heji Hospital affiliated to Changzhi Medical College Changzhi Shanxi China

Sponsors and Collaborators

  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences
  • Cangzhou Central Hospital
  • Weifang Medical University
  • Heji Hospital affiliated to Changzhi Medical College
  • Beijng Fengtai Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jianqiang Tang, Associate professor, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
ClinicalTrials.gov Identifier:
NCT05587452
Other Study ID Numbers:
  • NCC3511
First Posted:
Oct 20, 2022
Last Update Posted:
Oct 24, 2022
Last Verified:
Oct 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jianqiang Tang, Associate professor, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 24, 2022