EGFR mutations as biomarkers for targeted therapy

Since EGFR was discovered in 1978, our knowledge of its activating mutations and signaling pathways for cancer cell growth, proliferation and survival has continued to expand.1–3

The use of activating EGFR mutations as biomarkers has revolutionized the development of targeted TKI therapies to improve tumor response and patient outcomes in advanced NSCLC.2,3

In the era of precision medicine, determining the most effective NSCLC treatment strategy depends on the detection of EGFR mutations.2,3

EGFR sensitizing mutations have emerged as significant predictive and prognostic biomarkers for the selection of first-line TKI therapy and beyond2,3

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EGFR: epidermal growth factor receptor; NSCLC: non-small-cell lung cancer; TKI: tyrosine kinase inhibitor.