this single arm,open-label,multi-center study is aimed to evaluate the efficiency of icotinib in plasma ctDNA EGFR mutation-positive patients diagnosed with lung cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
120
Patients with plasma EGFR mutation-positive are arranged to receive icotinib with a dose of 125 mg three times per day, till progressive disease or unaccepted toxicity
National Cancer Center/Cancer Hospital
Beijing, Beijing Municipality, China
RECRUITINGORR
Objective Response Rate
Time frame: 12 weeks
PFS
Progression-free survival
Time frame: 12 months
DCR
disease control rate
Time frame: 12 months
OS
overall survival
Time frame: 20 months
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