About this trial
This is a prospective cohort study, which aims to evaluate the effectiveness and superiority of a novel minimal residual disease-guided prognosis monitoring and adjuvant treatment in stage IIA-IIIC non-small cell lung cancer.
Eligibility criteria
Qualifiers
Written informed consent must be signed before implementing any enrollment-related procedures;
Age ≥18 years old;
Patients with histologically or cytologically confirmed stage IIA-IIIC NSCLC (International Association for the Study of Lung Cancer and American Joint Committee on Classification of Cancer, 8th Edition TNM staging);
There is no special restriction on the source of genetic test report.
Disqualifiers
Received surgical treatment for lung tumors.
Received neoadjuvant chemotherapy or radiotherapy.
Received cellular therapy within the last 1 year.
Treated but uncontrolled diabetes, mellitus, asthma, autoimmune diseases and other chronic diseases.
Trial design
Treatments tested in this trial
- Operable