Risk stratification of EGFR
Brain metastases
EGFR(+) NSCLC
Overall survival
TP53 mutation
Treatment failure
Tyrosine kinase inhibitor
Journal
Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
25
05
2020
revised:
24
07
2020
accepted:
04
08
2020
pubmed:
2
9
2020
medline:
22
6
2021
entrez:
2
9
2020
Statut:
ppublish
Résumé
Panel-based next-generation sequencing (NGS) is increasingly used for the diagnosis of EGFR-mutated non-small-cell lung cancer (NSCLC) and could improve risk assessment in combination with clinical parameters. To this end, we retrospectively analyzed the outcome of 400 tyrosine kinase inhibitor (TKI)-treated EGFR EGFR alterations other than exon 19 deletions (non-del19), TP53 co-mutations, and brain metastases at baseline showed independent associations of similar strengths with progression-free (PFS hazard ratios [HR] 2.1-2.3) and overall survival (OS HR 1.7-2.2), in combination defining patient subgroups with distinct outcome (EGFR EGFR variant, TP53 status and brain metastases predict TKI efficacy and survival in EGFR
Identifiants
pubmed: 32871455
pii: S0169-5002(20)30579-1
doi: 10.1016/j.lungcan.2020.08.007
pii:
doi:
Substances chimiques
Protein Kinase Inhibitors
0
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105-112Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.