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

Molecular Typing System for Early Screening and Diagnosis of Lung Cancer Combined With Liquid Biopsy Technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05432128
Enrollment
600
Registered
2022-06-27
Start date
2020-01-01
Completion date
2025-12-31
Last updated
2024-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lung Cancer

Keywords

ctDNA methylation, AI analysis of LDCT images

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.

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.

Interventions

None listed

Sponsors

China-Japan Friendship Hospital
CollaboratorOTHER
Singlera Genomics Inc.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
To develop a molecular typing system for early screening and diagnosis of lung cancerassessed up to 36 monthsThe 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.
AI technology was combined with ctDNA methylation detection technologyassessed up to 36 monthsIn 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.

Countries

China

Contacts

Primary ContactMeng Yang, Bachelor
1943826591@qq.com18618307980
Backup ContactSinan Wu
tks0423@hotmail.com13810293738

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026