Clinical Trial Record

Return to Clinical Trials

Plasma Metabolic Biomarkers for Multi-Cancer Diagnosis


2024-03-29


2024-10


2025-04


2700

Study Overview

Plasma Metabolic Biomarkers for Multi-Cancer Diagnosis

The aim of this observational study is to comprehensively analyze the metabolites in plasma samples from multi-cancer patients using advanced mass spectrometry detection technology, in conjunction with metabolomics approaches. The goal is to construct a plasma metabolite database for multi-cancer patients. Simultaneously, we will delve into the exploration and validation of a series of metabolic biomarkers for early multi-cancer diagnosis. The objective is to establish a safer, more convenient, and more sensitive early screening method, thereby providing a reliable scientific foundation and critical evidence for improving the early diagnostic process for individuals at high risk of multi-cancer.

Firstly, a wide-targeted metabolomic measurement will be conducted on all samples to identify potential metabolite candidate markers and analyze differences in the metabolic profiles of patients with different types of cancer. Additionally, a comprehensive metabolite database specific to cancer patients will be constructed. Secondly, Samples will be randomly allocated into modeling and testing cohorts. The modeling cohort will be further divided into training and validation sets. Bioinformatics methods will be used to conduct an in-depth analysis of a wide range of metabolite information to screen out metabolic marker combinations with high diagnostic efficacy for cancer. Ultimately, the testing cohort will be used to validate these metabolic biomarkers, aiming to ensure reliability and stability across different patient populations.

  • Lung Cancer
  • Breast Cancer
  • Colorectal Cancer
  • Thyroid Cancer
  • Gastric Cancer
  • Cervical Cancer
  • Liver Cancer
  • Pancreatic Cancer
  • Cholangiocarcinoma
  • Prostate Cancer
  • Esophageal Cancer
  • Ovarian Cancer
  • Renal Cell Carcinoma
    • BFHHZML20240009

    Study Record Dates

    These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

    Study Registration Dates Results Reporting Dates Study Record Updates

    2024-04-09  

    N/A  

    2024-04-12  

    2024-04-09  

    N/A  

    2024-04-15  

    2024-04-12  

    N/A  

    2024-03  

    Study Plan

    This section provides details of the study plan, including how the study is designed and what the study is measuring.

    Design Details

    Primary Purpose:
    N/A


    Allocation:
    N/A


    Interventional Model:
    N/A


    Masking:
    N/A


    Arms and Interventions

    Participant Group/ArmIntervention/Treatment
    : Multi-cancer group

    Patients diagnosed with cancer, including lung cancer,breast cancer,colorectal cancer,thyroid cancer,gastric cancer,cervical cancer,liver cancer,pancreatic cancer,cholangiocarcinoma,prostate cancer,esophageal cancer,ovarian cancer,renal cell carcinoma.

    : control group

    Healthy controls

    Primary Outcome MeasuresMeasure DescriptionTime Frame
    Plasma metabolite contentThe outcome will be tested by metabolomics detection technology based on mass spectrometryBefore receiving treatment for cancer
    Secondary Outcome MeasuresMeasure DescriptionTime Frame

    Contacts and Locations

    This section provides the contact details for those conducting the study, and information on where this study is being conducted.

    Study Contact

    Name: Li Min, Ph.D.

    Phone Number: +86 13552652141

    Email: minli@ccmu.edu.cn

    Study Contact Backup

    Name: Bilian Kang, Ph.D.

    Phone Number: +86 18001218793

    Email: kbl@mail.ccmu.edu.cn

    Participation Criteria

    Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

    Ages Eligible for Study:
    ALL

    Sexes Eligible for Study:

    Accepts Healthy Volunteers:
    1

      Inclusion Criteria:

    • Multi-Cancer Group:


    • Patients with a confirmed diagnosis based on the clinical "gold standard".
    • Collection of plasma samples prior to treatment.
    • Availability of complete clinical data.
    • Control Group:


    • Individuals with no abnormalities in routine physical examinations and relevant clinical tests.
    • Age ≥ 45 years.
    • Availability of complete clinical data.

    • Exclusion Criteria:

    • Previous reception of anti-tumor treatments (including radiotherapy, chemotherapy, etc.) before blood collection.
    • Coexistence of other systemic tumors.
    • Absence of plasma sample collection before treatment.
    • Pregnancy status.
    • No clear evidence of histopathological diagnosis (not applicable to the control group based on this criterion).
    • Patients with severe acute infections.
    • Patients with severe anemia.
    • Patients with severe liver or kidney dysfunction.
    • Patients with autoimmune deficiency diseases.
    • Patients with Hyperlipidemia.
    • Patients received contrast agent injection before blood draw.
    • Patients with psychiatric disorders.

    Collaborators and Investigators

    This is where you will find people and organizations involved with this study.


      • PRINCIPAL_INVESTIGATOR: Li Min, Ph.D., Beijing Friendship Hospital

      Publications

      The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

      General Publications

      No publications available