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2000
Volume 14, Issue 2
  • ISSN: 1574-8871
  • E-ISSN: 1876-1038

Abstract

Background: Lung cancer is the leading cause of cancer mortality, being responsible for more than 1.6 million deaths each year worldwide and non-small-cell lung cancer (NSCLC) accounts for approximately 85% of lung cancers; moreover, 10 to 15% of all NSCLCs harbor EGFR (epidermal growth factor receptor) activating mutations, being suitable for EGFR-Tyrosine Kinase Inhibitors (TKI) molecular targeted therapy. However, EGFR+ NSCLCs gain acquired resistance to these agents, representing one of the key challenges for modern precision oncology. Objective: Therefore, this paper aims to provide an extensive state of the art review, alongside with hints about future perspectives. Conclusion: To date, in the light of the data from the FLAURA study, osimertinib represents the best first-line option in NSCLC patients with EGFR activating mutations; EGFR-TKI plus chemotherapy combination therapies, even though interesting, must still be considered investigational.

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/content/journals/rrct/10.2174/1574887114666181205155211
2019-06-01
2025-06-24
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/content/journals/rrct/10.2174/1574887114666181205155211
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  • Article Type:
    Review Article
Keyword(s): Combination therapy; EGFR; NSCLC; Osimertinib; T790M; TKI
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