Molecular residual disease analysis of adjuvant osimertinib in resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer

Thomas John 2
Christian Grohé 3
Jonathan H. Goldman 4
Terufumi Kato 5
Konstantin Laktionov 6
Laura Bonanno 7, 8
Marcello Tiseo 9
Margarita Majem 10
Manuel Dómine 11
Myung-Ju Ahn 12
Dariusz M. Kowalski 13
Maurice Perol 14
Virote Sriuranpong 15
Mustafa Özgüroğlu 16
Preetida Bhetariya 17
Aleksandra Markovets 17
Yuri Rukazenkov 18
Caitlin Muldoon 19
Jacqulyne P Robichaux 20
Ryan J. Hartmaier 20
Masahiro Tsuboi 21
Yi-Long Wu 22
3
 
Klinik für Pneumologie, Evangelische Lungenklinik Berlin Buch, Berlin, Germany
14
 
Department of Medical Oncology, Léon-Bérard Cancer Center, Lyon, France
17
 
Oncology Data Science, Oncology R&D, AstraZeneca, Boston, USA
20
 
Translational Medicine, Oncology R&D, AstraZeneca, Boston, USA
Publication typeJournal Article
Publication date2025-03-17
scimago Q1
wos Q1
SJR18.333
CiteScore82.4
Impact factor50.0
ISSN10788956, 1546170X, 17447933
Abstract
Osimertinib—a third-generation epidermal growth factor receptor-tyrosine kinase inhibitor—is recommended as adjuvant therapy for resected stage IB–IIIA epidermal growth factor receptor-mutated non-small-cell lung cancer, based on significant disease-free survival (DFS) and overall survival improvement shown in the previously reported phase 3 ADAURA trial. A trend toward an increased DFS event rate after completion of 3 years adjuvant treatment in ADAURA suggests that some patients may benefit from longer adjuvant osimertinib treatment. We therefore explored whether tumor-informed, circulating tumor DNA-based, molecular residual disease (MRD) could predict recurrence in an exploratory post hoc analysis of 220 patients (n = 112 osimertinib; n = 108 placebo) from ADAURA. MRD preceded imaging DFS events in this study by a median of 4.7 (95% confidence interval, 2.2–5.6) months. DFS and MRD event-free rate at 36 months was 86% versus 36% for patients in the osimertinib versus placebo groups (hazard ratio, 0.23 (95% confidence interval, 0.15–0.36)). In the osimertinib group, DFS or MRD events were detected in 28 (25%) patients; most events occurred following osimertinib cessation (19 of 28, 68%) and within 12 months of stopping osimertinib (11 of 19, 58%). At 24 months after osimertinib, the DFS and MRD event-free rate was 66%. In this study, MRD preceded DFS events in most patients across both arms. DFS and MRD event-free status was maintained for most patients during adjuvant osimertinib treatment and posttreatment follow-up, with most MRD or DFS events occurring after osimertinib treatment discontinuation or completion. MRD detection could potentially identify patients who may benefit from longer adjuvant osimertinib, although this requires clinical confirmation. ClinicalTrials.gov identifier: NCT02511106 . Exploratory post hoc analysis of molecular residual disease from the ADAURA trial of adjuvant osimertinib in patients with resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer shows that molecular residual disease detection predicts disease recurrence with long-term adjuvant osimertinib treatment.
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Herbst R. S. et al. Molecular residual disease analysis of adjuvant osimertinib in resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer // Nature Medicine. 2025.
GOST all authors (up to 50) Copy
Herbst R. S., John T., Grohé C., Goldman J. H., Kato T., Laktionov K., Bonanno L., Tiseo M., Majem M., Dómine M., Ahn M., Kowalski D. M., Perol M., Sriuranpong V., Özgüroğlu M., Bhetariya P., Markovets A., Rukazenkov Y., Muldoon C., Robichaux J. P., Hartmaier R. J., Tsuboi M., Wu Y. Molecular residual disease analysis of adjuvant osimertinib in resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer // Nature Medicine. 2025.
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TY - JOUR
DO - 10.1038/s41591-025-03577-y
UR - https://www.nature.com/articles/s41591-025-03577-y
TI - Molecular residual disease analysis of adjuvant osimertinib in resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer
T2 - Nature Medicine
AU - Herbst, Roy S.
AU - John, Thomas
AU - Grohé, Christian
AU - Goldman, Jonathan H.
AU - Kato, Terufumi
AU - Laktionov, Konstantin
AU - Bonanno, Laura
AU - Tiseo, Marcello
AU - Majem, Margarita
AU - Dómine, Manuel
AU - Ahn, Myung-Ju
AU - Kowalski, Dariusz M.
AU - Perol, Maurice
AU - Sriuranpong, Virote
AU - Özgüroğlu, Mustafa
AU - Bhetariya, Preetida
AU - Markovets, Aleksandra
AU - Rukazenkov, Yuri
AU - Muldoon, Caitlin
AU - Robichaux, Jacqulyne P
AU - Hartmaier, Ryan J.
AU - Tsuboi, Masahiro
AU - Wu, Yi-Long
PY - 2025
DA - 2025/03/17
PB - Springer Nature
SN - 1078-8956
SN - 1546-170X
SN - 1744-7933
ER -
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@article{2025_Herbst,
author = {Roy S. Herbst and Thomas John and Christian Grohé and Jonathan H. Goldman and Terufumi Kato and Konstantin Laktionov and Laura Bonanno and Marcello Tiseo and Margarita Majem and Manuel Dómine and Myung-Ju Ahn and Dariusz M. Kowalski and Maurice Perol and Virote Sriuranpong and Mustafa Özgüroğlu and Preetida Bhetariya and Aleksandra Markovets and Yuri Rukazenkov and Caitlin Muldoon and Jacqulyne P Robichaux and Ryan J. Hartmaier and Masahiro Tsuboi and Yi-Long Wu},
title = {Molecular residual disease analysis of adjuvant osimertinib in resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer},
journal = {Nature Medicine},
year = {2025},
publisher = {Springer Nature},
month = {mar},
url = {https://www.nature.com/articles/s41591-025-03577-y},
doi = {10.1038/s41591-025-03577-y}
}
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