TY - JOUR
T1 - Facteurs prédictifs de la réponse aux inhibiteurs de tyrosine kinase ciblant le récepteur à l'EGF dans le cancer bronchique
AU - De La Motte Rouge, Thibault
AU - Valent, Alexander
AU - Ambrosetti, Damien
AU - Vielh, Philippe
AU - Lacroix, Ludovic
PY - 2007/1/1
Y1 - 2007/1/1
N2 - Up to 10% of patients with non-small cell lung carcinoma (NSCLC) achieve an objective response to EGFR tyrosine kinase inhibitors (EGFR-TKI) such as erlotinib or gefitinib. This rate of response is related to non-smoker status, female gender, adenocarcinoma subtype, and Asian ethnicity. Molecular analysis showed that EGFR tyrosine kinase domain somatic mutations appear to be a strong predictor of response to EGFR-TKI. The L858R point mutation and the E746-A750 deletion represent 90% of the mutations encountered in responding patients. The amplification of EGFR gene also seems to be predictive of the response to EGFR-TKI, whereas T790M point mutation induces secondary resistance to EGFR-TKI.Nevertheless, objective responses or strong long-term stabilizations are observed in patients without any EGFR abnormality. Thus, the assessment of the EGFR status in patients with NSCLC remains controversial for clinical practice. The assessment of EGFR abnormalities should be targeted to identify reliable biomarkers of the NSCLC response to EGFR-TKI.This review presents the current knowledge on predictive biomarkers of NSCLC response to EGFR-TKI and the methods available for the assessment of EGFR status.
AB - Up to 10% of patients with non-small cell lung carcinoma (NSCLC) achieve an objective response to EGFR tyrosine kinase inhibitors (EGFR-TKI) such as erlotinib or gefitinib. This rate of response is related to non-smoker status, female gender, adenocarcinoma subtype, and Asian ethnicity. Molecular analysis showed that EGFR tyrosine kinase domain somatic mutations appear to be a strong predictor of response to EGFR-TKI. The L858R point mutation and the E746-A750 deletion represent 90% of the mutations encountered in responding patients. The amplification of EGFR gene also seems to be predictive of the response to EGFR-TKI, whereas T790M point mutation induces secondary resistance to EGFR-TKI.Nevertheless, objective responses or strong long-term stabilizations are observed in patients without any EGFR abnormality. Thus, the assessment of the EGFR status in patients with NSCLC remains controversial for clinical practice. The assessment of EGFR abnormalities should be targeted to identify reliable biomarkers of the NSCLC response to EGFR-TKI.This review presents the current knowledge on predictive biomarkers of NSCLC response to EGFR-TKI and the methods available for the assessment of EGFR status.
KW - Biomarkers
KW - EGFR
KW - Gene amplification
KW - Mutation
KW - Non-small cell lung cancer
KW - Tyrosine kinase inhibitors
UR - http://www.scopus.com/inward/record.url?scp=38049132443&partnerID=8YFLogxK
U2 - 10.1016/S0242-6498(07)78274-3
DO - 10.1016/S0242-6498(07)78274-3
M3 - Article
C2 - 18185470
AN - SCOPUS:38049132443
SN - 0242-6498
VL - 27
SP - 353
EP - 363
JO - Annales de Pathologie
JF - Annales de Pathologie
IS - 5
ER -