EGFR T790M resistance mutation in non small-cell lung carcinoma

Lung cancer patients carrying sensitive epidermal growth factor receptor (EGFR) mutations show dramatic responses to tyrosine kinase inhibitors (TKIs). However, the majority of patients whose disease responds to drugs eventually develop resistance to these EGFR-TKIs. The T790M gatekeeper mutation in...

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Veröffentlicht in:Clinica chimica acta 2015-04, Vol.444, p.81-85
Hauptverfasser: Denis, Marc G., Vallée, Audrey, Théoleyre, Sandrine
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container_title Clinica chimica acta
container_volume 444
creator Denis, Marc G.
Vallée, Audrey
Théoleyre, Sandrine
description Lung cancer patients carrying sensitive epidermal growth factor receptor (EGFR) mutations show dramatic responses to tyrosine kinase inhibitors (TKIs). However, the majority of patients whose disease responds to drugs eventually develop resistance to these EGFR-TKIs. The T790M gatekeeper mutation in the EGFR tyrosine kinase domain accounts for half of resistance to these drugs. In some patients, this mutation is also detected as a primary event before drug exposure, at a frequency that is highly dependent on the technique used. This review will focus on the methods that have been used to detect the T790M mutation, and its potential clinical applications both in TKI naïve patients and in patients with an acquired resistance. •The EGFR T790M mutation can be detected in some treatment naïve NSCLC.•The reported frequencies are highly dependent on the techniques used.•Patients presenting the T790M mutation respond to tyrosine kinase inhibitors.•The T790M mutation accounts for half of resistance to tyrosine kinase inhibitors.•New inhibitors seem to be efficient in patients who acquired the T790M mutation.
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subjects Carcinoma, Non-Small-Cell Lung - genetics
Drug Resistance, Neoplasm - genetics
EGFR
Humans
Lung Neoplasms - genetics
Mutation
Non small-cell lung cancer
Receptor, Epidermal Growth Factor - genetics
Receptor, Epidermal Growth Factor - metabolism
Resistance
T790M
title EGFR T790M resistance mutation in non small-cell lung carcinoma
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