Specimen and Clinical Data Collection Plan for LDCT Screening Participants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-74
SponsorChung Shan Medical University

About this trial

Lung cancer remains the leading cause of cancer-related mortality in Taiwan and globally, with increasing incidence and the highest healthcare cost burden among cancers in Taiwan. Despite the widespread use of low-dose computed tomography (LDCT) for screening smokers, over half of lung cancer cases in Taiwan occur in never-smokers, highlighting the need for improved risk stratification. Current national LDCT screening programs do not collect comprehensive risk-related data, limiting their predictive accuracy. This project proposes a five-year, multi-center initiative to establish an integrated biospecimen and clinical data collection system. In its first year, a feasibility pilot will be conducted, followed by recruitment of 12,000 participants. Data collection will include biospecimens (blood, urine, tissue), genomic and proteomic analyses, imaging, and detailed questionnaires covering lifestyle, environmental, and occupational exposures. The project will also develop and validate lung cancer prediction models incorporating epidemiologic, biomarker, air pollution, and imaging data. A Common Data Model (CDM) will be implemented to ensure cross-institutional data standardization and support future international collaboration.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

Pregnancy

History of chest computed tomography (including low-dose CT) within the past 12 months.

Previous diagnosis of lung cancer

Inability to undergo thoracic biopsy or surgery

Trial population

High risk population for lung cancer

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Specimen and clinical data collection

    Diagnostic test

    Check total bilirubin, urinary heavy metals,CRP, serum tumor marker, pulmonary function test,Questionnaire

Treatment groups

12,000 Participants
are divided into 2 treatment groups
Group A: Previous heavy smokers1 intervention
Group B: First degree relatives of lung cancer patients1 intervention

Trial outcomes

Primary outcomes

1

Definitive diagnosis of lung lesions confirmed by histopathological or cytological examination.

Time frame
Measured from time of suspicious imaging finding to histopathological or cytological diagnosis, within a 12 years period

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Chung Shan Medical University

Lead sponsor

National Health Research Institutes, Taiwan

Collaborator

Ministry of Health and Welfare

Collaborator