To Establish a Molecular Typing System for Early Diagnosis of Lung Cancer

Sponsor
Singlera Genomics Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05432128
Collaborator
China-Japan Friendship Hospital (Other)
600
1
36
16.7

Study Details

Study Description

Brief Summary

This topic to take large multicenter study real world, the advanced liquid biopsy will ctDNA methylation detection technique is applied to pulmonary nodules differential diagnosis and early lung cancer screening, validation of early lung cancer screening and diagnosis of molecular classification system model, the feasibility of the development of early lung cancer screening and diagnosis of molecular classification system, improve its early screening early detection accuracy and efficiency, Improve the survival status of lung cancer high-risk population. At the same time, this project combined AI analysis technology of LDCT image results with ctDNA methylation detection, so as to overcome false negatives caused by the deficiency of ctDNA methylation detection technology in sensitivity, specificity, stability and flux, and correct false positive results that may be caused by AI analysis technology of LDCT image results. The combination of the two can avoid missed diagnosis and over - examination and over - treatment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    1. All patients underwent low-dose CT pulmonary nodule AI detection and peripheral blood ctDNA methylation detection at baseline

    2. Follow-up plan: Low-risk and medium-risk nodules and some high-risk nodules (5-10mm) were followed up. 10ml peripheral blood was collected from each follow-up and stored for testing until the end of the study. The high-risk nodules over 10mm were evaluated by the expert group and the patients were informed by biopsy or surgical resection. Histopathological diagnosis was made and compared with ctDNA methylation results to analyze the sensitivity and specificity of ctDNA methylation markers of lung cancer.

    3. Endpoint: Tissue samples were pathologically diagnosed as benign or malignant.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    600 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Molecular Typing System for Early Screening and Diagnosis of Lung Cancer Combined With Liquid Biopsy Technology
    Actual Study Start Date :
    Jan 1, 2020
    Anticipated Primary Completion Date :
    Dec 31, 2022
    Anticipated Study Completion Date :
    Dec 31, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Low-risk group

    Combined with AI calculation of malignant probability and ctDNA methylation results, patients were divided into three groups. The high probability of malignancy calculated by AI was defined as positive, and vice versa. The methylation markers detected in specific peripheral blood of lung cancer were defined as positive, and vice versa. Negative for both items was considered as low risk group. Follow-up was conducted according to The Chinese Expert Consensus on the Diagnosis and Treatment of Pulmonary Nodules (2018 edition). 10ml peripheral blood was collected from each follow-up and stored for testing until the end of the study.

    medium-risk group

    As above, one positive patient was considered to be in the medium-risk group and was reexamined every 6 months, with a total of 3 reexaminations expected

    High-risk group

    Same as above, both positive are considered high-risk group.Part of high-risk nodules (5-10mm) will be reviewed every 3 months for the above two examinations, which is expected to be reviewed 6 times in total. Biopsy or surgical resection of high-risk nodules over 10mm will be performed after evaluation by the expert group and the patient's knowledge, and histopathological diagnosis will be made and compared with ctDNA methylation results. To analyze the sensitivity and specificity of ctDNA methylation markers in lung cancer.

    Outcome Measures

    Primary Outcome Measures

    1. To develop a molecular typing system for early screening and diagnosis of lung cancer [assessed up to 36 months]

      The feasibility of the molecular typing system model for early screening and diagnosis of lung cancer was verified through clinical studies, which significantly improved the accuracy and efficiency of early screening and early diagnosis, and improved the survival status of high-risk population of lung cancer.

    2. AI technology was combined with ctDNA methylation detection technology [assessed up to 36 months]

      In addition to overcoming false negatives caused by deficiencies in sensitivity, specificity, stability and flux of ctDNA methylation detection technology, and correcting false positive results that may be caused by AI, the combination of the two can avoid missed diagnosis, over-examination and over-treatment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients with pulmonary nodules confirmed by chest CT are not limited to single nodules;

    2. Nodule diameter 5-30mm

    3. Nodules include solid, semi-solid and ground glass nodules;

    4. Age 18-75, no gender limitation;

    5. The newly diagnosed patients did not receive surgery, radiotherapy, chemotherapy, targeted therapy or other tumor-related interventions;

    6. Sign informed consent.

    Exclusion Criteria:
    1. Patients with diagnosed lung cancer and extrapulmonary malignant tumor;

    2. Pulmonary sarcoidosis, pulmonary vasculitis, pulmonary tuberculosis;

    3. Patients with poor compliance are expected to be unable to complete follow-up according to the study protocol;

    4. Major trauma requiring blood transfusion occurred within one week before enrollment;

    5. Pregnant and lactation patients.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 China-Japan Friendship Hospital Beijing Beijing China 100029

    Sponsors and Collaborators

    • Singlera Genomics Inc.
    • China-Japan Friendship Hospital

    Investigators

    • Principal Investigator: Rui Liu, Doctor, Singlera Genomics Inc.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Singlera Genomics Inc.
    ClinicalTrials.gov Identifier:
    NCT05432128
    Other Study ID Numbers:
    • 2019YFC1315803
    First Posted:
    Jun 27, 2022
    Last Update Posted:
    Jun 27, 2022
    Last Verified:
    Jun 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Singlera Genomics Inc.
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 27, 2022