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Effects of icotinib on advanced non-small cell lung cancer with different EGFR phenotypes
Huiyun Pan1, Rong Liu, Shengjie Li
1Gerontology Center, The First Affiliated Hospital, Zhejiang University, No. 79, Qingchun Road, Hangzhou, 310003, Zhejiang, China.
Abstract:
Icotinib is the first oral epidermal growth factor receptor (EGFR) tyrosine kinase receptor inhibitor, which has been proven to exert significant inhibitory effects on non-small cell lung cancer in vitro. Clinical evidence has showed that the efficacy of Icotinib on retreating advanced non-small cell lung cancer is comparable to Gefitinib. However, different phenotypes of EGFR can affect the therapeutic outcomes of EGFR tyrosine kinase receptor inhibitor. Therefore, our study focused on efficacy and safety of Icotinib in patients with advanced non-small cell lung cancer of different EGPR phenotypes. Clinical data of patients with advanced non-small cell lung cancer who received Icotinib treatment from August, 2011 to May, 2013 were retrospectively analyzed. Kaplan-Meier analysis was used for survival analysis and comparison. 18 wild-type EGFR and 51 mutant type were found in a total of 69 patients. Objective response rate of patients with mutant type EGFR was 54.9 % and disease control rate was 86.3 %. Objective response rate of wild-type patients was 11.1 % (P = 0.0013 vs mutant type), disease control rate was 50.0 % (P = 0.0017). Median progression-free survival (PFS) of mutant type and wild-type patients were 9.7 and 2.6 months, respectively (P < 0.001). Median PFS of exon 19 mutated mutant patients was 11.3 months, mean PFS of exon 21 L858R mutated mutant patients was 8.7 months (P = 0.3145). Median overall survival (OS) of EGFR mutated patients had not reached. OS time of 13 wild-type patients was 12.9 months (P < 0.001). The common adverse reactions of Icotinib included rash, diarrhea, itching skin with occurrence rates of 24.6 % (17/69), 13.0 % (9/69), and 11.6 % (8/69), respectively. Most adverse reactions were grade I-II. Icotinib has great efficacy in EGFR mutated patients, making it an optimal regimen to treat EGFR mutated patients. Furthermore, most of adverse reactions associated with Icotinib treatment were tolerable.
Insights
Icotinib demonstrates significant efficacy in treating advanced non-small cell lung cancer, particularly in patients with epidermal growth factor receptor (EGFR) mutations. This targeted therapy shows comparable outcomes to Gefitinib, with manageable side effects.
Area of Science:
- Oncology
- Pharmacology
- Genetics
Background:
- Icotinib is an oral epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor effective against non-small cell lung cancer (NSCLC).
- Its efficacy in advanced NSCLC is comparable to Gefitinib, but EGFR phenotypes influence treatment outcomes.
- Understanding Icotinib's performance across different EGFR phenotypes is crucial for optimizing NSCLC treatment.
Purpose of the Study:
- To evaluate the efficacy and safety of Icotinib in advanced NSCLC patients with varying EGFR phenotypes.
- To compare treatment outcomes between EGFR wild-type and mutant NSCLC patients receiving Icotinib.
- To analyze survival data and adverse events associated with Icotinib therapy.
Main Methods:
- Retrospective analysis of clinical data from advanced NSCLC patients treated with Icotinib (August 2011 - May 2013).
- Kaplan-Meier analysis for survival analysis (progression-free survival and overall survival).
- Categorization of patients into EGFR wild-type (18) and mutant (51) groups.
Main Results:
- Icotinib showed significantly higher objective response rates (54.9% vs 11.1%) and disease control rates (86.3% vs 50.0%) in EGFR mutant vs wild-type patients (P < 0.0013).
- Median progression-free survival was substantially longer for EGFR mutant patients (9.7 months) compared to wild-type (2.6 months) (P < 0.001).
- Common adverse reactions included rash, diarrhea, and itching, mostly Grade I-II and tolerable.
Conclusions:
- Icotinib is highly effective and an optimal regimen for advanced NSCLC patients with EGFR mutations.
- Treatment outcomes differ significantly based on EGFR mutational status.
- Icotinib exhibits a favorable safety profile with manageable adverse events in NSCLC patients.
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