Phase
Condition
Lung Cancer
Lung Disease
Non-small Cell Lung Cancer
Treatment
12-month icotinib
6-month Icotinib
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Written informed consent provided.
Aged 18-75 years.
Had completely resected pathological confirmed stage IIA-IIIA NSCLC.
EGFR activating mutation in exon 19 or 21.
Had completed four cycles of platinum-based adjuvant chemotherapy.
Able to start the investigational therapy within 4 weeks after the completion offour cycles of adjuvant chemotherapy.
ECOG performance status of 0-1.
Had a life expectancy of 12 weeks or more.
Adequate hematological function, adequate liver function and renal function.
Able to comply with the required protocol and follow-up procedures, and able toreceive oral medications.
Female patients, except those who are postmenopausal or surgically sterilized, musthave a negative pre-study serum or urine pregnancy test.
Exclusion
Exclusion Criteria:
Had had previous chemotherapy besides four cycles of adjuvant chemotherapy,radiotherapy, or agents directed at the HER axis (e.g. erlotinib, gefitinib,cetuximab, trastuzumab).
Had a history another malignancy in the last 5 years with the exception of curedbasal cell carcinoma of the skin, cured in situ carcinoma of the uterine cervix andcured epithelial carcinoma of the bladder.
Any evidence confirmed tumor recurrence before investigational therapy.
Known severe hypersensitivity to icotinib or any of the excipients of this product.
Evidence of clinically active interstitial lung disease.
Eye inflammation not fully controlled or conditions predisposing the subject tothis.
Any unstable systemic disease (including active infection, uncontrolledhypertension, unstable angina, congestive heart failure, myocardial infarctionwithin the previous 6 months, serious cardiac arrhythmia requiring medication,hepatic, renal, or metabolic disease).
Known human immunodeficiency virus (HIV) infection.
Pregnancy or breast-feeding women.
Ingredients mixed with small cell lung cancer patients.
History of neurologic or psychiatric disorders.
Study Design
Study Description
Connect with a study center
Sun Yat-sen University Cancer Center
Guangzhou, Guangdong 510060
ChinaSite Not Available

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