High Efficacy of First-Line Gefitinib in Non-Asian Patients with EGFR-Mutated Lung Adenocarcinoma

Background: Several Asian studies demonstrated feasibility of front-line administration of gefitinib for the treatment of non-small cell lung carcinomas (NSCLCs) harboring intragenic epidermal growth factor receptor (EGFR) mutations. The experience of the use of this EGFR tyrosine kinase inhibitor (...

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Veröffentlicht in:Oncology research and treatment 2010-01, Vol.33 (5), p.231-238
Hauptverfasser: Moiseyenko, Vladimir M., Procenko, Svetlana A., Levchenko, Evgeny V., Barchuk, Alexey S., Moiseyenko, Fedor V., Iyevleva, Aglaya G., Mitiushkina, Nathalia V., Togo, Alexandr V., Semionov, Igor I., Ivantsov, Alexandr O., Matsko, Dmitry E., Imyanitov, Evgeny N.
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Sprache:eng
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Zusammenfassung:Background: Several Asian studies demonstrated feasibility of front-line administration of gefitinib for the treatment of non-small cell lung carcinomas (NSCLCs) harboring intragenic epidermal growth factor receptor (EGFR) mutations. The experience of the use of this EGFR tyrosine kinase inhibitor (TKI) in non-Asian subjects remains limited. Patients and Methods: The study included lung adenocarcinoma (AC) patients treated at the N.N. Petrov Institute of Oncology (Russia). Results: DNA analysis of 192 consecutive AC revealed 38 (20%) TKI-sensitizing mutations. Presence of the exon 19 deletion (del19) or L858R was strongly correlated with nonsmoking status (smokers: 8/98 (8%); non-smokers: 30/94 (32%); p = 0.00004). The efficacy of first-line gefitinib therapy was evaluated in 25 patients with EGFR-mutated advanced AC. Twelve (48%) cases demonstrated tumor response (1 (4%) complete response, 11 (44%) partial responses; 10/17 (59%) patients with del19 mutation vs. 2/8 (25%) cases with L858R substitution, p = 0.11). The remaining 13 (52%) patients experienced disease stabilization. Median progression-free survival was 8.0 months. Grade 3 toxicity was the maximal adverse event, being observed only in 4 (16%) cases. Conclusion: Gefitinib may be considered as an upfront treatment option for EGFR-mutated NSCLC.
ISSN:2296-5270
0378-584X
2296-5262
1423-0240
DOI:10.1159/000302729