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  4. Good response to gefitinib in lung adenocarcinoma of complex epidermal growth factor receptor (EGFR) mutations with the classical mutation pattern
 
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Good response to gefitinib in lung adenocarcinoma of complex epidermal growth factor receptor (EGFR) mutations with the classical mutation pattern

Journal
Oncologist
Journal Volume
13
Journal Issue
12
Pages
1276-1284
Date Issued
2008
Author(s)
SHANG-GIN WU  
YIH-LEONG CHANG  
Hsu Y.-C.
Wu J.-Y.
CHIH-HSIN YANG  
CHONG-JEN YU  
Tsai M.-F.
JIN-YUAN SHIH  
PAN-CHYR YANG  
DOI
10.1634/theoncologist.2008-0093
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-58749111646&doi=10.1634%2ftheoncologist.2008-0093&partnerID=40&md5=f1041c8a4904c17362d3c9dad9047679
https://scholars.lib.ntu.edu.tw/handle/123456789/473855
Abstract
Background. Epidermal growth factor receptor (EGFR) mutations are usually detected in lung adenocarcinoma and are associated with a response to EGFR tyrosine kinase inhibitors (TKIs). However, not all EGFR mutations have similarly high clinical response rates. This study aimed to investigate the clinical characteristics and response to gefitinib in lung adenocarcinoma patients with complex EGFR mutations. Materials and Methods. Three hundred thirty-nine specimens of lung adenocarcinoma from patients treated with gefitinib were collected for EGFR sequencing. Nineteen patients with complex EGFR mutations were enrolled for the study after excluding three patients with the EGFR T790M mutation, which confers resistance to gefitinib. Results. Among the 19 patients, 12 had complex mutations with the classical mutation pattern (L858R or deletion in exon 19). When compared with those without the classical mutation pattern, patients with this mutation pattern had a higher response rate (83% versus 29%), longer progression-free survival duration (median, 12.7 months versus 4.9 months), and longer overall survival time (median, 24.7 months versus 12.3 months) after gefitinib treatment. Comparing patients harboring complex EGFR mutations with a classical mutation pattern with those harboring single classical mutations, there were no statistical differences in the response rate (83% versus 73%), progression-free survival time (median, 12.7 months versus 8.1 months,) or overall survival time (median, 24.7 months versus 16.4 months). Conclusion. Patients with complex EGFR mutations with the classical mutation pattern had the same response rate, progression-free survival duration, and overall survival time as those with single classical mutations. EGFR TKIs may be the choice of treatment for this type of lung adenocarcinoma. ?AlphaMed Press.
SDGs

[SDGs]SDG3

Other Subjects
epidermal growth factor receptor; gefitinib; adult; aged; article; cancer growth; cancer staging; cancer survival; controlled study; female; gene mutation; gene sequence; human; human tissue; lung adenocarcinoma; major clinical study; male; mutational analysis; overall survival; priority journal; treatment response; Adenocarcinoma; Aged; Antineoplastic Agents; Female; Humans; Lung Neoplasms; Male; Middle Aged; Mutation; Protein Kinase Inhibitors; Quinazolines; Receptor, Epidermal Growth Factor
Type
journal article

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