Personalized care for patients with EGFR‐mutant nonsmall cell lung cancer: Navigating early to advanced disease management

M Maxime Borgeaud (Oncology Department University Hospital Geneva Geneva Switzerland) T Timothée Olivier (Oncology Department University Hospital Geneva Geneva Switzerland) J Jair Bar (Institute of Oncology Chaim Sheba Medical Center Ramat Gan Israel) S Stephanie Pei Li Saw (Division of Medical Oncology National Cancer Center Singapore Singapore) K Kaushal Parikh (Division of Medical Oncology Mayo Clinic Rochester Minnesota USA) G Giuseppe Luigi Banna (Department of Oncology Portsmouth Hospitals University National Health Service Trust Portsmouth UK) C Claudio De Vito (Pathology Department University Hospital Geneva Geneva Switzerland) J Jill Feldman (Patient Advocate EGFR Resisters Deerfield Illinois USA) X Xiuning Le (Department of Thoracic/Head and Neck Medical Oncology The University of Texas MD Anderson Cancer Center Houston Texas USA) A Alfredo Addeo (Oncology Department University Hospital Geneva Geneva Switzerland)

Abstract

AbstractThe discovery of activating mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the management of lung cancer, enabling the development of targeted tyrosine kinase inhibitors (TKIs). These therapies offer improved survival and reduced side effects compared with conventional treatments. Recent advancements have significantly reshaped the treatment paradigm for EGFR‐mutant non‐small cell lung cancer. TKIs are now incorporated into the management of early stage and locally advanced disease, and phase 3 trials have explored combination strategies in metastatic settings. Although these intensified approaches improve progression‐free survival, they come with increased toxicity and higher costs, underscoring the need for precise patient selection to maximize benefit. Emerging data on biomarkers, such as co‐mutations and circulating tumor DNA, show promise for refining treatment decisions. In addition, significant progress in understanding resistance mechanisms to EGFR TKIs has broadened therapeutic options. This review provides a comprehensive overview of the current landscape of EGFR‐mutant nonsmall cell lung cancer, highlighting recent breakthroughs and discussing strategies to optimize treatment based on the latest evidence.

Article Details

Volume / Issue Vol. 75, Issue 5
Published October 01, 2025
Pages 387-409
ISSN 0007-9235
Publisher Wiley

Journal Info

CA: A Cancer Journal for Clinicians

Wiley

ISSN: 0007-9235 Open Access Q1 Medicine

Authors (10)

M

Maxime Borgeaud

Oncology Department University Hospital Geneva Geneva Switzerland

T

Timothée Olivier

Oncology Department University Hospital Geneva Geneva Switzerland

J

Jair Bar

Institute of Oncology Chaim Sheba Medical Center Ramat Gan Israel

S

Stephanie Pei Li Saw

Division of Medical Oncology National Cancer Center Singapore Singapore

K

Kaushal Parikh

Division of Medical Oncology Mayo Clinic Rochester Minnesota USA

G

Giuseppe Luigi Banna

Department of Oncology Portsmouth Hospitals University National Health Service Trust Portsmouth UK

C

Claudio De Vito

Pathology Department University Hospital Geneva Geneva Switzerland

J

Jill Feldman

Patient Advocate EGFR Resisters Deerfield Illinois USA

X

Xiuning Le

Department of Thoracic/Head and Neck Medical Oncology The University of Texas MD Anderson Cancer Center Houston Texas USA

A

Alfredo Addeo

Oncology Department University Hospital Geneva Geneva Switzerland