Long-term Follow-up of Resected EGFR-mutated Non-small Cell Lung Cancer: A Real-world Study in a Portuguese Centre
DOI:
https://doi.org/10.20344/amp.23507Keywords:
Carcinoma, Non-Small-Cell Lung/surgery, ErbB Receptors/genetics, Mutation, Neoplasm StagingAbstract
Surgically resected epidermal growth factor receptor-mutated non-small cell lung cancer continues to carry a substantial risk of recurrence. The aim of this retrospective, single-center study, conducted at a Portuguese tertiary hospital was to evaluate the clinical course of these patients, diagnosed between 2016 and 2020, with the final clinical data review in November, 2024. A total of 48 patients were included, predominantly female (72.9%) and non-smokers (70.8%), most presenting exon 21 L858R or exon 19 deletion mutations. Mutations were identified by Sanger sequencing or next-generation sequencing. Programmed death-ligand 1 expression was < 1% in 58.3% of cases. At a median follow-up of 73.6 months, 31.3% of patients experienced relapse, all progressing to stage IV disease. The five-year disease-free survival and overall survival rates were 70% and 81%, respectively. Staging significantly influenced prognosis, with five-year disease-free survival ranging from 84% in stage IB to 20% in stage III. No significant differences were observed between epidermal growth factor receptor mutation subtypes. These findings are consistent with previous real-world studies and the placebo arm of the ADAURA trial, supporting the use of adjuvant osimertinib to reduce recurrence and improve long-term outcomes, while also emphasizing the need for improved perioperative risk assessment – including staging, histopathologic features, and molecular and genetic profiling – to guide personalized treatment.
Downloads
References
Li C, Lei S, Ding L, Xu Y, Wu X, Wang H, et al. Global burden and trends of lung cancer incidence and mortality. Chin Med J. 2023;136:1583-90. DOI: https://doi.org/10.1097/CM9.0000000000002529
Melosky B, Kambartel K, Häntschel M, Bennetts M, Nickens DJ, Brinkmann J, et al. Worldwide prevalence of epidermal growth factor receptor mutations in non-small cell lung cancer: a meta-analysis. Mol Diagn Ther. 2022;26:7-18. DOI: https://doi.org/10.1007/s40291-021-00563-1
National Comprehensive Cancer Network. Clinical practice guidelines in oncology (NCCN Guidelines®): non-small cell lung cancer. Version 3.2025. 2025. [cited 2025 Jan 30]. Available from: https://www.nccn.org/professionals/physician_gls/pdf/nscl.pdf.
Artal Cortés Á, Calera Urquizu L, Hernando Cubero J. Adjuvant chemotherapy in non-small cell lung cancer: state-of-the-art. Transl Lung Cancer Res. 2015;4:191-7.
Herbst RS, Wu YL, John T, Grohe C, Majem M, Wang J, et al. Adjuvant osimertinib for resected EGFR-mutated stage IB–IIIA non-small-cell lung cancer: updated results from the phase III randomized ADAURA trial. J Clin Oncol. 2023;41:1830-40. DOI: https://doi.org/10.1200/JCO.22.02186
Goldstraw P, Chansky K, Crowley J, Rami-Porta R, Asamura H, Eberhardt WE, et al. The IASLC lung cancer staging project: proposals for revision of the TNM stage groupings in the forthcoming, 8th ed. J Thorac Oncol. 2016;11:39-51. DOI: https://doi.org/10.1016/j.jtho.2015.09.009
Goldstraw P, Crowley J, Chansky K, Giroux DJ, Groome PA, Rami-Porta R, et al. The IASLC lung cancer staging project: proposals for the revision of the TNM stage groupings in the forthcoming. 7th ed. J Thorac Oncol. 2007;2:706-14. DOI: https://doi.org/10.1097/JTO.0b013e31812f3c1a
Auliac JB, Thomas PA, Bylicki O, Guisier F, Curcio H, Alain-Vegnenègre, et al. Resected EGFR-mutated non-small-cell lung cancers: incidence and outcomes in a European population (GFPC Exerpos Study). Ther Adv Med Oncol. 2024;16:17588359241236451. DOI: https://doi.org/10.1177/17588359241236451
Kuruvilla SM, Liu G, Syed I, Gwadry-Sridhar F, Sheffield BS, Sachdeva R, et al. EGFR mutation prevalence, real-world treatment patterns, and outcomes among patients with resected, early-stage, non-small cell lung cancer in Canada. Lung Cancer. 2022;173:58-66. DOI: https://doi.org/10.1016/j.lungcan.2022.08.023
Saw SP, Zhou S, Chen J, Lai G, Ang MK, Chua K, et al. Association of clinicopathologic and molecular tumor features with recurrence in resected early-stage epidermal growth factor receptor-positive non-small cell lung cancer. JAMA Netw Open. 2021;4:e2131892. DOI: https://doi.org/10.1001/jamanetworkopen.2021.31892
Wu YL, Liu SY, Wang Q, Zhou C, Lu S, Chen G, et al. A comprehensive model of genetic features predicts outcome of personalized adjuvant treatment in resected EGFR-mutant stage II–IIIA NSCLC: results from a phase III trial (CTONG 1104-ADJUVANT). Ann Oncol. 2019;30:v586. DOI: https://doi.org/10.1093/annonc/mdz258.002
Jao K, Tomasini P, Kamel-Reid S, Korpanty GJ, Mascaux C, Sakashita S, et al. The prognostic effect of single and multiple cancer-related somatic mutations in resected non-small-cell lung cancer. Lung Cancer. 2018;123:22-9. DOI: https://doi.org/10.1016/j.lungcan.2018.06.023
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Acta Médica Portuguesa

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
All the articles published in the AMP are open access and comply with the requirements of funding agencies or academic institutions. The AMP is governed by the terms of the Creative Commons ‘Attribution – Non-Commercial Use - (CC-BY-NC)’ license, regarding the use by third parties.
It is the author’s responsibility to obtain approval for the reproduction of figures, tables, etc. from other publications.
Upon acceptance of an article for publication, the authors will be asked to complete the ICMJE “Copyright Liability and Copyright Sharing Statement “(http://www.actamedicaportuguesa.com/info/AMP-NormasPublicacao.pdf) and the “Declaration of Potential Conflicts of Interest” (http:// www.icmje.org/conflicts-of-interest). An e-mail will be sent to the corresponding author to acknowledge receipt of the manuscript.
After publication, the authors are authorised to make their articles available in repositories of their institutions of origin, as long as they always mention where they were published and according to the Creative Commons license.

