About this trial
The purpose of this study is to determine whether ctDNA could help to evaluate whether to use drug adjuvant therapy after SBRT in patients with early lung cancer.
Eligibility criteria
Qualifiers
Patients pathologically diagnosed as non-small cell lung cancer, and was early stage(AJCC 8th);
Patients aged between 18 -80 years; with expected survival time>3 months.
blood routine examination criteria : i) hemoglobin (HB) ≥90g/L; ii) absolute neutrophil count (ANC) ≥1.5×10e9/L; iii) platelet (PLT) ≥80×10e9/L; b) biochemical tests meet the following criteria: i) total bilirubin (TBIL) ≤1.5 times of upper limit of normal (ULN); ii) alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 ULN; iii) serum creatinine (Cr) ≤1.5 ULN or creatinine clearance (CCr) ≥60mL/min;
Disqualifiers
Patients with small cell lung cancer (including small cell carcinoma and non-small cell carcinoma mixed lung cancer);
Patients with factors that affect oral medication (such as cannot swallow, chronic diarrhea and intestinal obstruction, etc.) or intravenous medication;
Patients with any other severe and/or uncontrolled disease;
Patients with a history of psychotropic medicine abuse and cannot quit or have mental disorders;
Trial design
Treatments tested in this trial
- drug adjuvant therapy