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Non-invasive multi-target examination in non-small cell lung cancer patients

Non-invasive multi-target examination in non-small cell lung cancer patients

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019169
Enrollment
Unknown
Registered
2018-10-29
Start date
2018-09-14
Completion date
Unknown
Last updated
2019-05-13

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

Conditions

non-small cell lung cancer

Interventions

Gold Standard:Tissue next genome sequencing detection
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Sponsors

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: (1) Clinically diagnosed patients with stage III and IV non-small cell lung cancer; (2) must have or can be obtained tissue samples of clinical routine genes (such as EGFR, ALK, ROS1, etc.) test results; (3) Patients with tumor tissue samples and blood samples can be taken at the same time; (4) Newly diagnosed and relapsed patients who had not been discharged within 6 months and treated with chemotherapy; (5) There was no clear evidence of other systemic malignancies when all cases were enrolled; (6) Complete records of clinical observations, imaging examinations, laboratory examinations; (7) Fixed at room temperature. Bronchoscopic biopsy specimens should be fixed within 6-24 hours; surgical specimens should be fixed within 12-48 hours; (8) Paraffin-embedded tumor samples and blood samples should be kept for less than 1 year.

Exclusion criteria

Exclusion criteria: (1) Subjects eventually diagnosed as other diseases, including pleural disease, mediastinal disease, chest wall tumors, etc.; (2) Subjects gave up surgery and related examinations for various reasons, and ultimately could not obtain pathological or cytological findings; (3) The clinical evaluator could not be completed because the physical condition was not related to the examination, refused to be examined, or was interrupted for other reasons.

Design outcomes

Primary

MeasureTime frame
ctDNA;

Countries

China

Contacts

Public ContactLI LIU

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

liulixiehe2004@163.com+86 027-85872015

Outcome results

None listed

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