About this trial
This study targeted patients with resectable stage II-IIIA non-small cell lung cancer with EGFR mutation
Eligibility criteria
Qualifiers
NSCLC patient with EGFR sensitive mutation as confirmed by needle biopsy;
At stage II-IIIA (TNM Staging, Version 8) as identified by chest CT, PET-CT or/and EBUS;
No systemic metastasis (confirmed by head MRI, whole body bone scan, PET-CT, liver and adrenal CT, etc.);
With the feasibility to receive radical surgery ;
Disqualifiers
The patient has undergone any systemic anti-cancer treatment for NSCLC, including surgical treatment, local radiotherapy, cytotoxic drug treatment, targeted drug treatment and experimental treatment, etc.;
The patient suffers from any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina pectoris, angina pectoris that starts to attack within the last 3 months, congestive heart failure [≥ Grade II specified by New York Heart Association (NYHA)], cardiac infarction (6 months before enrollment), severe arrhythmia and liver, kidney or metabolic diseases that requires drug treatment;
The patient is a carrier of HIV;
The patient has had or is currently suffering from interstitial lung disease;
Trial design
Treatments tested in this trial
- Befotertinib combined Bevacizumab
- Befotertinib combined platinum-based double chemotherapy
Treatment groups
Sponsors and collaborators
Peng Zhang
Lead sponsor
Shanghai Pulmonary Hospital, Shanghai, China
Sponsor institution