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Correlation analysis of the tumour immune microenvironment of lung adenocarcinoma patients with their clinicopathological features, immune response and postoperative survival

Correlation analysis of the tumour immune microenvironment of lung adenocarcinoma patients with their clinicopathological features, immune response and postoperative survival

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096467
Enrollment
Unknown
Registered
2025-01-24
Start date
2025-01-25
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Lung cancer

Interventions

None:None

Sponsors

Shandong University of Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years old 2. All patients were treated for the first time and confirmed as lung adenocarcinoma by postoperative histopathology 3. The postoperative tumor staging of all patients was classified as stage?-? 4. All subjects showed no abnormalities in vital signs, electrocardiogram and laboratory tests 5. No clear history of the central nervous system, cardiovascular system, kidney, liver, digestive tract, respiratory system, metabolism, or musculoskeletal system 6. Informed consent of the person or authorized client 7. Did not participate in any other study 8. Regular follow-up can be performed

Exclusion criteria

Exclusion criteria: 1. Previous history of other malignant tumors 2. Positive surgical margin 3. Had received any anti-tumor treatment such as radiotherapy, chemotherapy, immunotherapy and preoperative neoadjuvant therapy before surgery 4. Clinical evidence of any infectious inflammatory condition such as fever and chills within 1 month before surgery 5. Use of any drugs that may affect the results of hematological examination within 1 month before surgery 6. Preoperative complications such as liver disease, blood system disease or severe organ failure 7. Any other clinically significant disease or condition that was considered by the investigator to be likely to affect adherence to the protocol or to affect informed consent or to preclude participation in the study If the answer was "yes" to any of the above, they could not enter the study.

Design outcomes

Primary

MeasureTime frame
Multi-immune site studies of regulatory T cells and others in the immune microenvironment;Single-cell RNA sequencing (scRNA-seq) of surgically resected tumour tissues from 30 postoperative patients with lung adenocarcinoma and gene expression profiling of cancer cells and immunity to fine at the single-cell level;

Countries

China

Contacts

Public ContactZhang Jingshun

Affiliated Hospital of Shandong University of Traditional Chinese Medicine

415381984@qq.com+86 151 9216 1337

Outcome results

None listed

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