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

Autor: Hélène Blons, Benjamin Besse, Jérôme Solassol, Michèle Legrain, Isabelle Rouquette, P. de Cremoux, Ivan Bièche, Anne-Claire Voegeli, Pascale Tomasini, Jacques Cadranel, Marie Wislez, F. De Fraipont, Laurence Baudrin, Fabienne Escande, Jean-Luc Prétet, Elisabeth Quoix, E. Favre-Guillevin, Nathalie Prim, Franck Morin, Roger Lacave, Ludovic Lacroix, A.-M. Ruppert, Isabelle Nanni-Metellus, Sarab Lizard, Anne Cayre, Gérard Zalcman, Michèle Beau-Faller

Publikováno v: Annals of Oncology
Annals of Oncology, Oxford University Press (OUP), 2014, 25, pp.126--31. ⟨10.1093/annonc/mdt418⟩
Annals of Oncology, 2014, 25, pp.126--31. ⟨10.1093/annonc/mdt418⟩
Annals of Oncology, Elsevier, 2014, 25, pp.126--31. ⟨10.1093/annonc/mdt418⟩

International audience; BACKGROUND: There is scarce data available about epidermal growth factor receptor (EGFR) mutations other than common exon 19 deletions and exon 21 (L858R) mutations. PATIENTS AND METHODS: EGFR exon 18 and/or exon 20 mutations

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f9bdfc634c42ac78a34089935ed1474
https://hal.umontpellier.fr/hal-02181347

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