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Study on tumor microenvironment and evolution mechanism of lung cancer

Study on tumor microenvironment and evolution mechanism of lung cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100053858
Enrollment
Unknown
Registered
2021-12-01
Start date
2021-11-26
Completion date
Unknown
Last updated
2022-10-31

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

Conditions

Lung cancer

Interventions

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Be able to provide written informed consent (ICF), and be able to understand and agree to abide by the research requirements and evaluation schedule, and be able to cooperate in observing adverse events and curative effects. 2. No gender limit, aged 18-75 years at the time of signing the ICF. 3. Untreated advanced (III or IV) non-small cell lung cancer patients. 4. Have clear genetic test results. 5. ECOG PS: 0-2, and no signs of tumor progression in the last 2 weeks. 6. Expected survival time > 12 weeks. 7. The non-acute inflammatory period when the sample was collected.

Exclusion criteria

Exclusion criteria: 1. Patients receiving other approved systemic immunomodulators (including but not limited to interferon, interleukin 2, and tumor necrosis factor) 8 weeks prior to the first dose. 2. Active autoimmune disease that requires systemic treatment, and the investigator evaluates patients who are considered to have an impact on the study treatment. 3. Patients with long-term heavy use of hormones or other immunosuppressive agents, and the investigators assess that they have an impact on the study treatment. 4. Severe chronic or active infections requiring systemic antibacterial, antifungal or antiviral treatment, including tuberculosis infection, etc.: (1) Serious infection requiring hospitalization before the first administration or within 4 weeks of the peripheral blood collection time point, including but not limited to complications of infection, bacteremia or severe pneumonia; (2) Received oral or intravenous antibiotic therapy within 2 weeks before the first dose. 5. Known human immunodeficiency virus (HIV) infection. 6. Participate in another therapeutic clinical study at the same time. 7. Presence of a high-risk underlying medical condition or alcohol/drug abuse or dependence that affects the study.

Design outcomes

Primary

MeasureTime frame
Lung cancer tumor immune microenvironment heterogeneity;

Countries

China

Contacts

Public ContactTian Panwen

West China Hospital of Sichuan University

mrascend@163.com+86 13550351753

Outcome results

None listed

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