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A Non-Interventional Systematic Study for the Non-Small Cell Lung Cancer Tempo-spatial Heterogeneity

A Non-Interventional Systematic Study for the Non-Small Cell Lung Cancer Tempo-spatial Heterogeneity

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022521
Enrollment
Unknown
Registered
2019-04-15
Start date
2017-04-01
Completion date
Unknown
Last updated
2019-04-23

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

Case series:No intervention

Sponsors

Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 years; 2. Pathologically confirmed patients with resectable stage I-IIIA non-small cell lung cancer; 3. Patient follow-up information is complete, and plasma and peripheral blood samples, as well as paraffin and/or fresh tissue samples of surgical tissue can be obtained; 4. Patients with multiple primary or metastatic lesions (lymph nodes or solitary metastases, etc.) were preferentially enrolled in the group; 5. Subjects read and fully understand the patient's instructions and sign informed consent.

Exclusion criteria

Exclusion criteria: 1.For patients who are unable to obtain tissue and blood samples, blood samples should include at least two time points: pre-operative (d0) and post-operative (d7); 2.Current alcoholics or drug abusers; 3.pregnant women, women planning to become pregnant, or women who are breast feeding should not participate in the study; 4.Active infections of clinical significance or any form of acute disease; 5.The patient had a history of other tumors or had received antineoplastic treatment before admission. 6.It is estimated that patients' compliance to participate in this clinical study is insufficient. 7.Received other drug clinical trials in the past 4 weeks.

Design outcomes

Primary

MeasureTime frame
next generation sequencing;

Secondary

MeasureTime frame
progression-free survival;overall survival;

Countries

China

Contacts

Public ContactLin Xu
xulin83@gmail.com+86 13605168383

Outcome results

None listed

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