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EGFR Exon 20 Insertion in Metastatic Non-Small-Cell Lung Cancer: Survival and Clinical Efficacy of EGFR Tyrosine-Kinase Inhibitor and Chemotherapy.
Chelabi, Samy; Mignard, Xavier; Leroy, Karen; Monnet, Isabelle; Brosseau, Solenn; Theou-Anton, Nathalie; Massiani, Marie-Ange; Friard, Sylvie; Duchemann, Boris; Fabre, Elizabeth; Giroux-Leprieur, Etienne; Cadranel, Jacques; Wislez, Marie.
Afiliação
  • Chelabi S; Oncology Thoracic Unit, Pulmonology Department, AP-HP, Hôpital Cochin, F-75014 Paris, France.
  • Mignard X; Oncology Thoracic Unit, Pulmonology Department, AP-HP, Hôpital Cochin, F-75014 Paris, France.
  • Leroy K; Biochemistry Department, AP-HP, Hôpital Européen Georges Pompidou, F-75015 Paris, France.
  • Monnet I; Team Inflammation, Complement, and Cancer, Centre de Recherche des Cordeliers, Université de Paris, Sorbonne Université, INSERM, F-75006 Paris, France.
  • Brosseau S; Department of Pulmonology, Centre Hospitalier Intercommunal de Créteil, F-94000 Créteil, France.
  • Theou-Anton N; Department of Thoracic Oncology, AP-HP, Hôpital Bichat-Claude Bernard, F-75018 Paris, France.
  • Massiani MA; Department of Genetic, AP-HP, Hôpital Bichat-Claude Bernard, F-75018 Paris, France.
  • Friard S; Department of Medical Oncology, Institut Curie, F-92210 Saint-Cloud, France.
  • Duchemann B; Department of Pulmonology, Hôpital Foch, F-92150 Suresnes, France.
  • Fabre E; Department of Thoracic and Medical Oncology, AP-HP, Hôpital Avicenne, F-93000 Bobigny, France.
  • Giroux-Leprieur E; Department of medical Oncology, APHP, Hôpital Européen Georges Pompidou, F-75015 Paris, France.
  • Cadranel J; INSERM U970, Université Paris Descartes, F-75015 Paris, France.
  • Wislez M; Department of Respiratory Diseases and Thoracic Oncology, APHP, Hôpital Ambroise Paré, F-92100 Boulogne-Billancourt, France.
Cancers (Basel) ; 13(20)2021 Oct 13.
Article em En | MEDLINE | ID: mdl-34680280
ABSTRACT
EGFR exon 20 insertions are rare genetic alterations in non-small-cell lung cancers (NSCLCs) that are usually unresponsive to approved EGFR tyrosine kinase inhibitors (TKIs). In this paper, we describe the clinical characteristics, efficacy of EFGR TKIs and chemotherapy, and resulting survival in this population. We retrospectively collected patients with EGFR exon 20 insertions (Exon20ins) from 11 French genetic platforms and paired them (12 ratio) with classic Exon 19/21 EGFR mutation patients (controls). Between 2012 and 2017, 35 Exon20ins patients were included. These patients were younger at diagnosis than the controls. All Exon20ins patients who were treated with first-line EGFR TKIs (n = 6) showed progressive disease as the best tumor response. There was no significant difference in the tumor response or the disease control rate with first-line platinum-based chemotherapy between the two groups. A trend towards shorter overall survival was observed in Exon20ins vs. controls (17 months (14-not reach(NR) 95% confidence interval(CI) vs. 29 months (17-NR 95%CI), p = 0.09), respectively. A significant heterogeneity in amino acid insertion in EGFR exon 20 was observed. EGFR exon 20 insertions are heterogeneous molecular alterations in NSCLC that are resistant to classic EGFR TKIs, which contraindicates their use as a first-line treatment.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article