Skip to content

To explore Multi-platform solution of pulmonary occasional nodules early diagnose and follow up by using ctDNA Methylation sequencing based on NGS and lung cancer auto antibody molecular detection technology.

To explore Multi-platform solution of pulmonary occasional nodules early diagnose and follow up by using ctDNA Methylation sequencing based on NGS and lung cancer auto antibody molecular detection technology.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015749
Enrollment
Unknown
Registered
2018-04-18
Start date
2018-05-01
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

Lung Cancer

Interventions

Gold Standard:Fleischner Society 2017 Guidelines for Management of Incidentally Detected Pulmonary Nodules in Adults
ctNDA&#32
Lung&#32
cancer&#32
autoantibody&#32

Sponsors

Guangdong General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Pulmonary occasional nodules subject detected by LDCT; 2. Age >=18 year, and sign ICF; 3. Never received any surgery,radiotherapy,chemotherapy or moleculary targeted anti-tumor treatment; 4. Never diagnosed NSCLC by tumor histology or cytology; 5. No specific tuberculosis, inflammation or pulmonary benign nodules which diagnosed clearly; 6. At least one measurable pulmonary benign nodules by LDCT examination; 7. Exclude having obvious maligancy pulmonary tumor indications people which define as CEA increased above 10 times normal value; 8. Exclude having obvious benign pulmonary nodules indications people which define as tuberculosis or inflammation indicator positive; 9. Subject was consent and able to follow the study visit plan, and to provide 10ml blood sample prior to any clinical treatment and future follow-up visit, and to cooperate other study procedures.

Exclusion criteria

Exclusion criteria: 1. Subject have serious disease that may likely impact follow-up and short-term survial judged by investigaor; 2. Subject had been received any surgery,radiotherapy,chemotherapy or moleculary targeted anti-tumor treatment; 3. Subject had been received antituberculous or antifungal treamtent wich target on nodules; 4. Subject have specific active effection, including but not limited pneumonia; 5. Subject have obvious maligancy pulmonary tumor indications people which define as CEA increased above 10 times normal value; 6. Subject have obvious benign pulmonary nodules indications people which define as tuberculosis or inflammation indicator positive; 7. Subject is not appropriate for enrollment that judge by investigator.

Design outcomes

Primary

MeasureTime frame
blood ctDNA methylatiion;Lung cancer autoantibody detection;

Countries

China

Contacts

Public ContactGuibin Qiao

Guangdong General Hospital

qiaoguibin@163.com+86 020-83827812

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026