This study was a single-arm, multi-center, prospective, phase 3 trial aimed to evaluate the efficacy and safety of icotinib in patients with locally advanced or metastatic NSCLC after failure of at least one platinum-based chemotherapy regimen.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
128
Patients were administered with oral icotinib (tablet form, 125 mg) three times daily within two days after enrollment until disease progression or unacceptable toxicity.
Cancer Hospital, Chinese Academy of Medical Science
Beijing, Beijing Municipality, China
Peking Union Medical College Hospital
Beijing, Beijing Municipality, China
Bejing Cancer Hospital
Beijing, Beijing Municipality, China
progression-free survival
Time frame: 6 months
overall survival
Time frame: 12 months
objective response rate
Time frame: 2 months
number of patients suffered adverse events
Time frame: 15 months
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307 Hospital of PLA
Beijing, Beijing Municipality, China
Beijing Chest Hospital
Beijing, Beijing Municipality, China
Third Affiliated Hospital, Third Military Medical University
Chongqing, Chongqing Municipality, China
Sun yat-sen Univerisity Cancer Center
Guanzhou, Guangdong, China
Jiangsu Cancer Hospital
Nanjing, Jiangsu, China
Shanghai Pulmonary Hospital
Shanghai, Shanghai Municipality, China
The First Affiliated Hospital of College of Medicine, Zhejiang University
Hangzhou, Zhejiang, China