TY - JOUR
T1 - Clinical Activity of Afatinib in Patients With Non–Small-Cell Lung Cancer Harboring Uncommon EGFR Mutations
T2 - A Spanish Retrospective Multicenter Study
AU - Moran, Teresa
AU - Taus, Alvaro
AU - Arriola, Edurne
AU - Aguado, Carlos
AU - Dómine, Manuel
AU - Rueda, Ana Gómez
AU - Calles, Antonio
AU - Cedrés, Susana
AU - Viñolas, Nuria
AU - Isla, Dolores
AU - Palmero, Ramón
AU - Sereno, María
AU - Diaz, Victor
AU - Juan, Oscar
AU - Marsé, Raquel
AU - Martorell, Paloma Martín
AU - Sánchez Torres, José Miguel
AU - Anguera, Georgia
AU - Bosch, Joaquim
AU - Cabezón, Luis
AU - Catot, Silvia
AU - Martinez, Alex
AU - Muñoz, Silvia
AU - Ramos, Inmaculada
N1 - Publisher Copyright:
© 2020 Elsevier Inc.
PY - 2020/9
Y1 - 2020/9
N2 - We report the results of the molecular and clinical characterization and the efficacy of afatinib in a cohort of patients with advanced non–small-cell lung cancer (NSCLC) patients harboring uncommon epidermal growth factor receptor (EGFR) mutations in Spanish clinical practice. In patients with uncommon EGFR-mutant NSCLC, the most common mutations occurred on exon 18 in amino acid G719, either alone or in combination with another mutation; other uncommon mutations were detected in exons 18, 19, 20, 21, and 22. In clinical practice, afatinib was active in patients with uncommon EGFR-mutant NSCLC, particularly in patients with complex and single mutations; however, in patients with EGFR ins20 (EGFR exon 20 insertions), treatment with afatinib provided a lower clinical benefit, indicating that further treatment strategies are needed for patients with this type of uncommon EGFR mutation.
AB - We report the results of the molecular and clinical characterization and the efficacy of afatinib in a cohort of patients with advanced non–small-cell lung cancer (NSCLC) patients harboring uncommon epidermal growth factor receptor (EGFR) mutations in Spanish clinical practice. In patients with uncommon EGFR-mutant NSCLC, the most common mutations occurred on exon 18 in amino acid G719, either alone or in combination with another mutation; other uncommon mutations were detected in exons 18, 19, 20, 21, and 22. In clinical practice, afatinib was active in patients with uncommon EGFR-mutant NSCLC, particularly in patients with complex and single mutations; however, in patients with EGFR ins20 (EGFR exon 20 insertions), treatment with afatinib provided a lower clinical benefit, indicating that further treatment strategies are needed for patients with this type of uncommon EGFR mutation.
KW - Afatinib
KW - EGFR mutations
KW - NSCLC
KW - Retrospective
KW - Uncommon
UR - http://www.scopus.com/inward/record.url?scp=85085203444&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2020.04.011
DO - 10.1016/j.cllc.2020.04.011
M3 - Article
C2 - 32461037
AN - SCOPUS:85085203444
SN - 1525-7304
VL - 21
SP - 428-436.e2
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 5
ER -