Different prognostic role of EGFR mutation according to the IASLC histological grade in patients with resected early‐stage lung adenocarcinoma

Author:

Hong Tae H12,Hwang Soohyun3ORCID,Choi Yoon‐La3,Lee Genehee45,Park Sehhoon6,Ahn Myung‐Ju6,Lee Yoonseo1,Jeon Yeong J1,Lee Junghee1,Shin Sumin17,Park Seong Y1,Cho Jong H1,Choi Yong S1,Kim Jhingook1,Shim Young M14,Cho Juhee458,Kim Hong K145

Affiliation:

1. Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Korea

2. Department of Digital Health SAIHST, Sungkyunkwan University Seoul Korea

3. Department of Pathology and Translational Genomics, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Korea

4. Samsung Medical Center Patient‐Centered Outcomes Research Institute Seoul Korea

5. Department of Clinical Research Design and Evaluation SAIHST, Sungkyunkwan University Seoul Korea

6. Division of Hematology‐Oncology, Department of Medicine, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul Korea

7. Department of Thoracic and Cardiovascular Surgery School of Medicine, Ewha Womans University, Mok‐Dong Hospital Seoul Korea

8. Center for Clinical Epidemiology, Samsung Medical Center Future Medicine Institute Seoul Korea

Abstract

AimsThe prognostic role of EGFR mutations remains controversial. We aimed to evaluate the prognostic role of EGFR mutation in consideration of the IASLC histological grade in patients with resected early‐stage lung adenocarcinoma.Methods and resultsA total of 3297 patients with stages I–IIA resected lung adenocarcinoma who had had EGFR mutation tests between January 2014 and December 2019 at the Samsung Medical Center, Seoul, Korea were included. Recurrence‐free survival (RFS) was compared by EGFR mutation status (EGFR‐M+ versus EGFR‐WT) and IASLC histological grade (G1, G2 and G3). Cox proportional hazards models were used to estimate the adjusted HRs (aHRs) and 95% confidence intervals (CIs).ResultsCompared to the EGFR‐WT group, the EGFR‐M+ group had a significantly lower proportion of G3 tumour (16 versus 33%, P < 0.001). During a median follow‐up of 41.4 months, 376 patients experienced recurrence. After adjusting for histological grade, the aHR for recurrence comparing the EGFR‐M+ to the EGFR‐WT was 1.30 (95% CI = 1.04–1.62, P = 0.022). The EGFR‐M+ group had a significantly lower 5‐year RFS than the EGFR‐WT group among G3 patients (58.4 versus 71.5%, P < 0.001), but not among G1 and G2 patients.ConclusionsEGFR mutation status was associated with a risk of recurrence after consideration of the IASLC histological grading, especially in G3 tumours. The results of this study would be useful for developing a new staging system and identifying a subset of patients who may benefit from adjuvant targeted therapy.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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