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Clinical experience with gefitinib: an update

  • Federico Cappuzzo
  • , Giovanna Finocchiaro
  • , Giulio Metro
  • , Stefania Bartolini
  • , Elisabetta Magrini
  • , Alessandra Cancellieri
  • , Rocco Trisolini
  • , Luciano Castaldini
  • , Giovanni Tallini
  • , Lucio Crino
  • Ospedale Bellaria

Research output: Contribution to journalArticle

Abstract

Gefitinib is an orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that blocks signal transduction pathways involved in cell proliferation. This drug demonstrated impressive and durable responses in patients with heavily pretreated non-small cell lung cancer (NSCLC). In two large phase II trials, responses were observed in 9-19% of unselected patients, along with symptom improvement and benefit in quality of life. Biological mechanisms underlying TKI sensitivity have recently been discovered. There is evidence that specific EGFR gene mutations and/or amplification confer a particularly sensitive phenotype, especially in individuals with tumors demonstrating activation of the anti-apoptotic protein Akt. However, in all so far conducted clinical trials, no patient selection has been made, providing a logical explanation for the negative results observed in large phase III studies. In the present review, we will summarize the results observed in clinical trials with gefitinib. We will present results obtained in NSCLC and in other solid tumor, focusing on biological and clinical markers predicting drug sensitivity. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)31-45
Number of pages15
JournalCritical Reviews in Oncology/Hematology
Volume58
DOIs
Publication statusPublished - 2006

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
  • gefitinib
  • non-small cell lung cancer
  • tyrosine kinase inhibitor

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