The emerging role of epidermal growth factor receptor (EGFR) inhibitors in first-line treatment for patients with advanced non-small cell lung cancer positive for EGFR mutations

Author:

Okamoto Isamu1,Mitsudomi Tetsuya2,Nakagawa Kazuhiko3,Fukuoka Masahiro4

Affiliation:

1. Department of Medical Oncology, Kinki University School of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan chi-okamoto@ dotd.med.kindai.ac.jp

2. Department of Thoracic Surgery, Aichi Cancer Center Hospital, Nagoya, Japan

3. Department of Medical Oncology, Kinki University School of Medicine, Osaka, Japan

4. Department of Medical Oncology, Kinki University School of Medicine, Sakai Hospital, Osaka, Japan

Abstract

Gefitinib and erlotinib, small-molecule tyrosine kinase inhibitors (TKIs) of the epidermal growth factor receptor (EGFR), were the first molecularly targeted agents to become clinically available for the treatment of non-small cell lung cancer (NSCLC). During the course of their clinical development, it has become clear that the substantial clinical benefit associated with EGFR-TKIs is limited to patients harboring activating mutations of EGFR. Accumulating clinical outcomes in patients with EGFR mutation-positive NSCLC treated with EGFR-TKIs support the notion that this group of individuals constitutes a clinically distinct population. These findings have prompted investigations of the potential role of first-line treatment with EGFR-TKIs in molecularly selected patients, with platinum-based doublet chemotherapy currently being the standard of care for most individuals with advanced NSCLC. This review summarizes the results of recent clinical trials of EGFR-TKIs in selected patients and highlights the efficacy of these drugs in first-line treatment as a form of personalized medicine aimed at improving therapy for advanced NSCLC.

Publisher

SAGE Publications

Subject

Oncology

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