PT - JOURNAL ARTICLE AU - Bogdan Grigoriu AU - Thierry Berghmans AU - Anne-Pascale Meert TI - Management of EGFR mutated nonsmall cell lung carcinoma patients AID - 10.1183/09031936.00156614 DP - 2015 Apr 01 TA - European Respiratory Journal PG - 1132--1141 VI - 45 IP - 4 4099 - http://erj.ersjournals.com/content/45/4/1132.short 4100 - http://erj.ersjournals.com/content/45/4/1132.full SO - Eur Respir J2015 Apr 01; 45 AB - Tyrosine kinase inhibitors (TKIs) targeting the epidermal growth factor receptor (EGFR) are common in the therapeutic armentarium of lung cancer today. Initially tested in an unselected population, they have been of limited usefulness until the identification EGFR gene mutations. Activating mutations generate conformational changes that result in a shift toward an active state of the catalytic domain and are associated with sensitivity to first generation EGFR TKI. Other mutations have been associated with resistance to these drugs, but for rare mutations there is limited data concerning their role in predicting response to EGFR TKI.To date, four molecules have been approved for the treatment of EGFR mutated lung cancer. Gefitinib and/or erlotinib are available in almost all countries. Afatinib has been approved by the US Food and Drug Administration and by the European Medicines Agency, and icotinib has been approved only in China. Other, more active, third generation agents with a higher binding affinity for the receptor, or that are directed against specific mutations, are under development. EGFR TKIs have a favourable impact on progression-free survival when given as first line treatment in mutated patients, but may also have a moderate effect as a salvage therapy and in maintenance in an unselected population.All patients with nonsquamous nonsmall cell lung cancer must be tested for the presence of EGFR activating mutations http://ow.ly/IdivY