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Clinical Trials in China / NCT07242482
Starting soon Observational

Circulating Immune Markers for Prognostic Evaluation in Postoperative Lung Cancer Patients

NCT07242482 · tracked via the Priya Life Science China tracker
Sponsor
Zhao Jun
Phase
Observational
Started
2025-12-17
Last updated
2025-11-21

Condition(s) studied

Lung Cancer (Diagnosis)Biomarkers / Blood

Investigational drug(s) / intervention(s)

Preoperative Peripheral Blood Immune Marker Analysis.

Preoperative Peripheral Blood Immune Marker Analysis.: Preoperative collection of approximately 5 mL peripheral blood via venipuncture, followed by isolation of peripheral blood mononuclear cells (PBMCs) using Ficoll density gradient centrifugation. PBMCs are analyzed via multiparametric flow cytometry on a BD FACSCanto II system to quantify antigen-specific effector T cells (ETASTs, co-expressing CD137 and IFN-γ after ex vivo stimulation with NSCLC antigen peptide pools like NY-ESO-1 and MAGE-A3) and the effector T cell to regulatory T cell ratio (Teff/Treg, with Teff as CD4+/CD8+ expressing IFN-γ/TNF-α/IL-2 and Treg as CD4+CD25+FoxP3+). Analysis uses FlowJo software, targeting 100,000 events per sample. This non-invasive prognostic assessment is distinct from routine clinical blood tests by its focus on tumor-specific immune activation and balance, without therapeutic intent or alteration of standard care.

Study summary

Investigating the Clinical Value of Tumor Antigen-Specific T Cells and Immune Cell Balance in Peripheral Blood of Non-Small Cell Lung Cancer Patients for Prognostic Evaluation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18 to 80 years. * Diagnosed with primary non-small cell lung cancer (NSCLC) and scheduled to undergo curative lung resection at the Department of Thoracic Surgery of our institution. * Postoperative pathological stage is IB (with tumor size \>4cm or high-risk factors: poor differentiation, vascular invasion, visceral pleural invasion, sub-lobar resection, etc.), IIA, IIB, or IIIB (according to the AJCC 8th edition). * ECOG performance status of 0 or 1. * Voluntarily signs the informed consent form. Exclusion Criteria: * Received any neoadjuvant therapy prior to surgery. * History of other active malignancies. * Diagnosed with severe autoimmune diseases, active infections, or immunodeficiency disorders. * Presence of severe cardiac, hepatic, or renal dysfunction. * Pregnant or lactating women.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Soochow university, Suzhou, Jiangsu 215000 Suzhou Jiangsu

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07242482 on ClinicalTrials.gov ↗ ← All trials in China