This is a single-armed study designed to evaluate the safety and efficacy of adjuvant targeted-therapy in patients with epidermal growth factor receptor mutation positive stage IB-IIA non-small cell lung carcinoma and high-risk of recurrence following complete tumor resection. The primary endpoint: 2-year DFS rate; The second endpoint: DFS
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
90
Furmonertinib (80 mg orally, once daily) for 3 years.
Shanghai General Hospital
Shanghai, Shanghai Municipality, China
RECRUITINGDisease Free Survival (DFS) rate at 2 years
Assess the Efficacy of Adjuvant Furmonertinib as Measured by 2-year Disease Free Survival (DFS) rate.
Time frame: From date of receiving therapy until date of disease recurrence or death (by any cause in the absence of recurrence), up to approximately 4 years. Assessed at 2 years.
Disease Free Survival (DFS)
Assess the Efficacy of Adjuvant Furmonertinib as Measured by Disease Free Survival (DFS).
Time frame: From date of receiving therapy until date of disease recurrence or death (by any cause in the absence of recurrence), up to approximately 4 years.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.