Fast Facts: EGFR Exon 20 Insertion Mutations in NSCLC von Julia Rotow | ISBN 9783318070200

Fast Facts: EGFR Exon 20 Insertion Mutations in NSCLC

von Julia Rotow, Parneet Cheema, Pasquale Pisapia und Giancarlo Troncone
Mitwirkende
Autor / AutorinJulia Rotow
Autor / AutorinParneet Cheema
Autor / AutorinPasquale Pisapia
Autor / AutorinGiancarlo Troncone
Buchcover Fast Facts: EGFR Exon 20 Insertion Mutations in NSCLC | Julia Rotow | EAN 9783318070200 | ISBN 3-318-07020-3 | ISBN 978-3-318-07020-0
Inhaltsverzeichnis 1

Fast Facts: EGFR Exon 20 Insertion Mutations in NSCLC

von Julia Rotow, Parneet Cheema, Pasquale Pisapia und Giancarlo Troncone
Mitwirkende
Autor / AutorinJulia Rotow
Autor / AutorinParneet Cheema
Autor / AutorinPasquale Pisapia
Autor / AutorinGiancarlo Troncone
Lung cancer is still a major cause of death globally, but the development of personalized, precision medicine has had a marked effect on treatment management and improved clinical outcomes, particularly for those with advanced stage non-small-cell lung cancer (NSCLC). EGFR mutations are the third most common mutation found in patients with advanced stage NSCLC. First-line treatment with a traditional epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) is indicated for most patients, but not for patients with EGFR exon 20 insertion mutations (ex20ins). Instead, recent approvals of an EGFR ex20ins-specific TKI (mobocertinib) and a bispecific antibody (amivantamab) targeting both EGFR and mesenchymalepithelial transition factor (MET) offer the potential for improved outcomes in this patient population. Furthermore, new approaches to treatment continue to be developed and trials for new agents with greater activity against ex20ins mutations are ongoing.