TY - JOUR
T1 - Utilizing ctDNA to discover mechanisms of resistance to targeted therapies in patients with metastatic NSCLC
T2 - towards more informative trials
AU - Ernst, Sophie M.
AU - Aldea, Mihaela
AU - von der Thüsen, Jan H.
AU - de Langen, Adrianus J.
AU - Smit, Egbert F.
AU - Paats, Marthe S.
AU - Aerts, Joachim G.J.V.
AU - Mezquita, Laura
AU - Popat, Sanjay
AU - Besse, Benjamin
AU - Remon, Jordi
AU - Rolfo, Christian
AU - Dubbink, Hendrikus J.
AU - Dingemans, Anne Marie C.
N1 - Publisher Copyright:
© Springer Nature Limited 2025.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - Advances in targeted therapies for patients with non-small-cell lung cancer have substantially improved the outcomes of those with actionable alterations in certain oncogenic driver genes. However, acquired resistance to these targeted therapies remains a major challenge. Understanding the mechanisms underlying acquired resistance will be crucial for the development of strategies that might either overcome this effect or delay the onset. Circulating tumour DNA, owing to the need for only minimally invasive sampling and a potential role as both a prognostic and predictive biomarker, is increasingly being used in both research and clinical practice. Several studies have explored the landscape of acquired resistance to targeted therapies using this approach. However, the methodologies of the published studies vary widely, and several major challenges remain in addressing the practical difficulties associated with these methods. These challenges currently limit the depth of research insight provided by the available data. In this Perspective, we review clinical reports describing the use of circulating tumour DNA to detect mechanisms of acquired resistance to targeted therapies, predominantly in patients with advanced-stage non-small-cell lung cancer, and highlight key unresolved questions with the aim of moving towards more-informative research studies.
AB - Advances in targeted therapies for patients with non-small-cell lung cancer have substantially improved the outcomes of those with actionable alterations in certain oncogenic driver genes. However, acquired resistance to these targeted therapies remains a major challenge. Understanding the mechanisms underlying acquired resistance will be crucial for the development of strategies that might either overcome this effect or delay the onset. Circulating tumour DNA, owing to the need for only minimally invasive sampling and a potential role as both a prognostic and predictive biomarker, is increasingly being used in both research and clinical practice. Several studies have explored the landscape of acquired resistance to targeted therapies using this approach. However, the methodologies of the published studies vary widely, and several major challenges remain in addressing the practical difficulties associated with these methods. These challenges currently limit the depth of research insight provided by the available data. In this Perspective, we review clinical reports describing the use of circulating tumour DNA to detect mechanisms of acquired resistance to targeted therapies, predominantly in patients with advanced-stage non-small-cell lung cancer, and highlight key unresolved questions with the aim of moving towards more-informative research studies.
UR - http://www.scopus.com/inward/record.url?scp=105000416473&partnerID=8YFLogxK
U2 - 10.1038/s41571-025-01011-3
DO - 10.1038/s41571-025-01011-3
M3 - Article
AN - SCOPUS:105000416473
SN - 1759-4774
JO - Nature Reviews Clinical Oncology
JF - Nature Reviews Clinical Oncology
M1 - 105074
ER -