Third-line Treatment of Gefitinib in NSCLC Patients

1. The subject or legal guardian could understand and sign informed consent form.
2. Male or female aged 18 years or older;
3. Subjects were diagnosed with stage IIIB or IV NSCLC before starting the first dose of gefitinib third-line treatment;
4. EGFR exon 19 deletion or exon 21 L858R substitution mutation confirmed;
5. ECOG performance status 0-2;
6. Life expectancy of at least 12 weeks or longer;
7. Has at least one measureable lesion by RECIST 1.1;
8. NSCLC of enrolled subjects previously progressed after first-line gefitinib treatment (PFS ≥ 6 months) and progressed again after second-line chemotherapy (not limited for chemotherapy regimen, ≥ 4 cycles of chemotherapy). Investigator considers adopting third-line gefitinib retreatment;

9. Criteria for laboratory examinations:

   • Total bilirubin (TB) ≤ 1.5 times upper limit of normal
   • Aspartate aminotransferase(AST), alanine aminotransferase (ALT) ≤2 times upper limit of normal; for subjects with hepatic metastasis, AST,ALT≤ 5 times upper limit of normal
   • Creatinine clearance≥45ml/min

Exclusion Criteria:

1. Known severe hypersensitivity to gefitinib or any ingredients of the product;
2. Patients with prior exposure to agents directed at the EGFR axis except gefitinib (e.g. erlotinib, cetuximab, trastuzumab) ;
3. Pre-existing interstitial lung disease or pulmonary fibrosis evidenced by CT scan at baseline;
4. Neutrophil count \<1.0×109/L or platelet count \<50×109/L;
5. Severe infection, uncontrolled systemic disease (e.g cardiopulmonary insufficiency, fatal arrhythmias, hepatitis, etc);
6. Pregnancy or breast-feeding;
7. Women of childbearing age refuse to take adequate contraception measures during gefitinib treatment
8. Subjects with other malignant tumors combined;
9. Known or suspected brain metastases or spinal cord compression, unless treated with surgery and/or radiation and stable without steroid treatment for at least 4 weeks prior to the first dose of study medication;
10. Subjects are unable to take medications orally or have digestive malabsorption;
11. Investigators consider subjects should not be involved in the study.