Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor–Resistant Disease

Author:

Ohashi Kadoaki1,Maruvka Yosef E.1,Michor Franziska1,Pao William1

Affiliation:

1. Kadoaki Ohashi and William Pao, Vanderbilt University School of Medicine, Nashville, TN; and Yosef E. Maruvka and Franziska Michor, Dana-Farber Cancer Institute and Harvard School of Public Health, Boston, MA.

Abstract

Purpose EGFR-mutant lung cancer was first described as a new clinical entity in 2004. Here, we present an update on new controversies and conclusions regarding the disease. Methods This article reviews the clinical implications of EGFR mutations in lung cancer with a focus on epidermal growth factor receptor tyrosine kinase inhibitor resistance. Results The discovery of EGFR mutations has altered the ways in which we consider and treat non–small-cell lung cancer (NSCLC). Patients whose metastatic tumors harbor EGFR mutations are expected to live longer than 2 years, more than double the previous survival rates for lung cancer. Conclusion The information presented in this review can guide practitioners and help them inform their patients about EGFR mutations and their impact on the treatment of NSCLC. Efforts should now concentrate on making EGFR-mutant lung cancer a chronic rather than fatal disease.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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