<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>25(1)</volume><submitter>Beau-Faller M</submitter><funding>French</funding><funding>National Cancer Institute</funding><funding>Ligue Nationale Contre le Cancer</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>There is scarce data available about epidermal growth factor receptor (EGFR) mutations other than common exon 19 deletions and exon 21 (L858R) mutations.&lt;h4>Patients and methods&lt;/h4>EGFR exon 18 and/or exon 20 mutations were collected from 10 117 non-small-cell lung cancer (NSCLC) samples analysed at 15 French National Cancer Institute (INCa)-platforms of the ERMETIC-IFCT network.&lt;h4>Results&lt;/h4>Between 2008 and 2011, 1047 (10%) samples were EGFR-mutated, 102 (10%) with rare mutations: 41 (4%) in exon 18, 49 (5%) in exon 20, and 12 (1%) with other EGFR mutations. Exon 20 mutations were related to never-smoker status, when compared with exon 18 mutations (P &lt; 0.001). Median overall survival (OS) of metastatic disease was 21 months [95% confidence interval (CI) 12-24], wor</pubmed_abstract><journal>Annals of oncology : official journal of the European Society for Medical Oncology</journal><pagination>126-31</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3868323</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Rare EGFR exon 18 and exon 20 mutations in non-small-cell lung cancer on 10 117 patients: a multicentre observational study by the French ERMETIC-IFCT network.</pubmed_title><pmcid>PMC3868323</pmcid><pubmed_authors>Nanni-Metellus I</pubmed_authors><pubmed_authors>Lacroix L</pubmed_authors><pubmed_authors>Blons H</pubmed_authors><pubmed_authors>Lacave R</pubmed_authors><pubmed_authors>Escande F</pubmed_authors><pubmed_authors>Prim N</pubmed_authors><pubmed_authors>Bieche I</pubmed_authors><pubmed_authors>Rouquette I</pubmed_authors><pubmed_authors>Pretet JL</pubmed_authors><pubmed_authors>Voegeli AC</pubmed_authors><pubmed_authors>Baudrin L</pubmed_authors><pubmed_authors>Morin F</pubmed_authors><pubmed_authors>Besse B</pubmed_authors><pubmed_authors>Zalcman G</pubmed_authors><pubmed_authors>Solassol J</pubmed_authors><pubmed_authors>de Fraipont F</pubmed_authors><pubmed_authors>de Cremoux P</pubmed_authors><pubmed_authors>Cayre A</pubmed_authors><pubmed_authors>Lizard S</pubmed_authors><pubmed_authors>Tomasini P</pubmed_authors><pubmed_authors>Cadranel J</pubmed_authors><pubmed_authors>Beau-Faller M</pubmed_authors><pubmed_authors>Quoix E</pubmed_authors><pubmed_authors>Favre-Guillevin E</pubmed_authors><pubmed_authors>Legrain M</pubmed_authors><pubmed_authors>Ruppert AM</pubmed_authors><pubmed_authors>Wislez M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rare EGFR exon 18 and exon 20 mutations in non-small-cell lung cancer on 10 117 patients: a multicentre observational study by the French ERMETIC-IFCT network.</name><description>&lt;h4>Background&lt;/h4>There is scarce data available about epidermal growth factor receptor (EGFR) mutations other than common exon 19 deletions and exon 21 (L858R) mutations.&lt;h4>Patients and methods&lt;/h4>EGFR exon 18 and/or exon 20 mutations were collected from 10 117 non-small-cell lung cancer (NSCLC) samples analysed at 15 French National Cancer Institute (INCa)-platforms of the ERMETIC-IFCT network.&lt;h4>Results&lt;/h4>Between 2008 and 2011, 1047 (10%) samples were EGFR-mutated, 102 (10%) with rare mutations: 41 (4%) in exon 18, 49 (5%) in exon 20, and 12 (1%) with other EGFR mutations. Exon 20 mutations were related to never-smoker status, when compared with exon 18 mutations (P &lt; 0.001). Median overall survival (OS) of metastatic disease was 21 months [95% confidence interval (CI) 12-24], wor</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Jan</publication><modification>2026-04-14T17:14:46.034Z</modification><creation>2025-07-28T03:04:09.49Z</creation></dates><accession>S-EPMC3868323</accession><cross_references><pubmed>24285021</pubmed><doi>10.1093/annonc/mdt418</doi></cross_references></HashMap>