The ctDNA for Evaluating Whether to Use Adjuvant Therapy After SBRT in Patients With Early Lung Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorPeking University Third Hospital

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

Treatment groups

180 Participants
are divided into 3 treatment groups