Abstract

Lung adenocarcinomas are more commonly associated with brain metastases (BM). Epidermal growth factor receptor (EGFR) mutations have been demonstrated to be both predictive and prognostic for patients with lung adenocarcinoma. We aimed to explore the potential association between EGFR mutation and the risk of BM in pulmonary adenocarcinoma patients. Data of 234 patients from 2007 to 2014 were retrospectively reviewed. A total of 108 patients had EGFR mutations in the entire cohort. Among them, 76 patients developed BM during their disease course. The incidence of BM was statistically higher in patients with EGFR mutations both at initial diagnosis (P=0.014) and at last follow-up (P<0.001). Multivariate logistic regression analysis revealed that EGFR mutation significantly increased the risk of BM at initial diagnosis (OR=2.515, P=0.022). In patients without BM at initial diagnosis, the accumulative rate of subsequent BM was significantly higher with EGFR mutations (P=0.001). Multivariate Cox regression analysis identified EGFR mutation as the only independent risk factor for subsequent BM (HR=3.036, P=0.001). Patients with EGFR mutations demonstrated longer overall survival (OS) after BM diagnosis than patients with wild-type EGFR (P=0.028). Our data suggest that EGFR mutation is an independent predictive and prognostic risk factor for BM and a positive predictive factor for OS in patients with BM.

Highlights

  • 80% of lung cancer cases have been classified as non-small cell lung carcinoma (NSCLC), which can be further divided into subtypes according to specific histology such as adenocarcinoma, squamous cell carcinoma, and large cell carcinoma [1]

  • Studies have shown that adenocarcinoma histology is associated with a significantly higher incidence of brain metastases (BM) than other subtypes of NSCLC [1, 23, 24]

  • We retrospectively evaluated the different features of BM according to Epidermal growth factor receptor (EGFR) mutation status in patients with pulmonary adenocarcinoma

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Summary

Introduction

80% of lung cancer cases have been classified as non-small cell lung carcinoma (NSCLC), which can be further divided into subtypes according to specific histology such as adenocarcinoma, squamous cell carcinoma, and large cell carcinoma [1]. Among these pathological subtypes, adenocarcinoma is the most common subtype; which occurs in more than half of NSCLC patients. 45-52% of patients with lung adenocarcinoma develop BM at some point in their disease course, which compares unfavorably with a less than 20% incidence of BM for squamous cell carcinoma [5, 6]. The prognosis for patients with BM remains poor, with a median overall survival (OS) of 2-3 months when treated with systemic corticosteroid alone, and a median OS of 3-6 months when treated with whole brain radiation therapy (WBRT) [7, 8]

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