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Poster Display session

173P - Clinical and pathological insights into EGFR-mutated early-stage non-small cell lung cancer (NSCLC): Associations with survival, PD-L1 expression, and second primary neoplasms

Date

28 Mar 2025

Session

Poster Display session

Presenters

Benedetta Del Rio

Citation

Journal of Thoracic Oncology (2025) 20 (3): S98-S120. 10.1016/S1556-0864(25)00632-X

Authors

B. Del Rio1, H. Bote-De Cabo2, M. Peressini ??lvarez2, C. Serrano Gomez2, J. Torres Jimenez2, M. Zurera Berjaga2, S. Masini3, O.C. García2, D. Pelegrina2, J.A. Nunez Sobrino2, V. Adradas2, S. Ponce Aix2, L. Paz-Ares2, J. Zugazagoitia4, J. Baena Espinar4

Author affiliations

  • 1 Azienda Ospedaliera Universitaria San Luigi Gonzaga, Orbassano/IT
  • 2 Hospital Universitario 12 de Octubre, Madrid/ES
  • 3 Humanitas University, Milan/IT
  • 4 Hospital Universitario 12 Octubre, Madrid/ES

Resources

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Abstract 173P

Background

Early-stage EGFR-mutated (EGFRmut) NSCLC is poorly characterized. This study analyzed clinical and pathological features in a Spanish cohort.

Methods

A retrospective review of resected EGFRmut stage I-III NSCLC cases was conducted in Hospital 12 de Octubre, with mutations identified by real time-PCR or NGS. Survival was analyzed using Kaplan-Meier and Cox models, and associations were tested with Chi-square and Fisher’s exact tests.

Results

Between April 2011 and January 2022, 76 NSCLC EGFRmut patients underwent curative-intent surgery. Median age was 70.5 years, 62% were women, 50% non-smokers, 74% had a performance status (PS) of 0.74% were stage I, 83% had common EGFRmut (51% exon 19 deletions, 32% exon 21 L858R) and 6.6% exon 20 insertions. PD-L1 was ≥1 in 27% and 50% had co-mutations (detected by NGS). Some 29 patients had additional malignancies before (53.6%) and after (46.4%) NSCLC diagnosis. After a median follow-up of 79.7 months, up to 22 patients (29%) had recurrences. The median disease-free survival (DFS) and overall survival (OS) were not reached (71% without relapse and 77.3 % alive). PS (PS 1–2 vs PS 0) and staging (stage II–III vs stage I) were associated with DFS (HR=5.02, CI: 2.09–12.03; HR=1.8, CI: 1.4–2.3 respectively) and OS (HR=6.2, CI: 2.5–15.3; HR=2.0, CI: 1.3–2.6 respectively) in univariable and multivariable analysis (DFS HR=3.3, CI: 1.15–9.52; HR=5.3, CI: 1.9–14.5; OS HR=6.2, CI: 1.99–19.57; HR=4.6, CI: 1.48–14.34 respectively). Furthermore, a correlation between tobacco exposure and PD-L1 expression was observed (p=0.002). Additional malignancy was correlated with PD-L1 expression (p=0.003) but not with tobacco (p=0.5). Additionally, co-mutations were more prevalent in L858R EGFRmut tumors (p=0.007).

Conclusions

This study describes a real-world early-stage EGFRmut NSCLC population with outcomes similar to those reported in the literature. Survival outcomes were significantly associated with cancer stage and PS. Moreover, our study reveals a high prevalence of additional neoplasms and suggests that tobacco exposure may affect PD-L1 expression in patients with early-stage EGFRmut NSCLC.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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