TY - JOUR
T1 - Clinical experience with gefitinib: an update
AU - Cappuzzo, Federico
AU - Finocchiaro, Giovanna
AU - Metro, Giulio
AU - Bartolini, Stefania
AU - Magrini, Elisabetta
AU - Cancellieri, Alessandra
AU - Trisolini, Rocco
AU - Castaldini, Luciano
AU - Tallini, Giovanni
AU - Crino, Lucio
PY - 2006
Y1 - 2006
N2 - 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.
AB - 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.
KW - EGFR
KW - non-small cell lung cancer
KW - gefitinib
KW - tyrosine kinase inhibitor
KW - EGFR
KW - non-small cell lung cancer
KW - gefitinib
KW - tyrosine kinase inhibitor
UR - http://hdl.handle.net/10807/282179
U2 - 10.1016/j.critrevonc.2005.08.008
DO - 10.1016/j.critrevonc.2005.08.008
M3 - Article
SN - 1040-8428
VL - 58
SP - 31
EP - 45
JO - CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
JF - CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY
ER -