About this trial
This project aims to innovatively integrate multi-omics data, including plasma metabolomics, radiomics, and cfDNA multi-level information, combined with survival data (e.g., RFS), to establish a novel multidimensional approach for noninvasive postoperative recurrence monitoring in lung cancer using artificial intelligence algorithms. The goal is to develop a new noninvasive recurrence monitoring system for lung cancer.
Eligibility criteria
Qualifiers
Signed written informed consent.
Male or female, aged ≥ 18 and < 85 years.
Radical resection performed, pathologic stage IB-IIIA (8th TNM) non-small-cell lung cancer.
Tumor tissue and blood samples obtainable at all protocol-specified time-points.
Disqualifiers
Postoperative pathology shows other than NSCLC, including but not limited to benign lesions, small-cell carcinoma, metastasis, or indeterminate/inadequate histology.
Insufficient or poor-quality blood or tissue samples.
Pure ground-glass nodule on imaging.
History of any malignancy within the past 5 years.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Locations
1Sponsors and collaborators
Peking University People's Hospital
Lead sponsor