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Afatinib and lung cancer

  • Prantesh Jain
  • , Rashmi Khanal
  • , Aakanksha Sharma
  • , Yan Feng
  • , Neelesh Sharma
  • Cleveland Clinic Foundation
  • Roswell Park Comprehensive Cancer Center
  • KLE Academy of Higher Education and Research, Belagavi
  • Bristol-Myers Squibb
  • Case Western Reserve University

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI) have an established role in the treatment of non-small-cell lung cancer (NSCLC). First-generation reversible ATP-competitive EGFR-TKIs are approved for the initial treatment of patients with EGFR mutation-positive advanced NSCLC. Afatinib is an irreversible second-generation EGFR-TKI with potent preclinical activity against EGFR (wild type and mutant), HER2, HER4 and EGFR-mutant NSCLC with acquired resistance to reversible EGFR-TKI. LUX-Lung 3 trial demonstrated superiority of afatinib to cisplatin and pemetrexed in the frontline treatment of treatment-naïve patients with advanced adenocarcinoma of the lung and EGFR mutation. Based on these results, afatinib was recently approved for the first-line treatment of NSCLC patients with EGFR mutation. This article summarizes current status of preclinical and clinical development of afatinib in NSCLC.

Original languageEnglish
Pages (from-to)1391-1406
Number of pages16
JournalExpert Review of Anticancer Therapy
Volume14
Issue number12
DOIs
StatePublished - Nov 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • EGFR
  • NSCLC
  • afatinib
  • erlotinib
  • gefitinib

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