Abstract

Epidermal growth factor receptor (EGFR) mutations are the strongest response predictors to EGFR tyrosine kinase inhibitors (TKI) therapy, but knowledge of the EGFR mutation frequency on lung adenocarcinoma is still limited to retrospective studies. The PIONEER study (NCT01185314) is a prospective molecular epidemiology study in Asian patients with newly diagnosed advanced lung adenocarcinoma, aiming to prospectively analyze EGFR mutation status in IIIB/IV treatment-naïve lung adenocarcinomas in Asia. We report the mainland China subset results. Eligible patients (≥20 yrs old, IIIB/IV adenocarcinoma and treatment-naïve) were registered in 17 hospitals in mainland China. EGFR was tested for mutations by amplification refractory mutation system using biopsy samples. Demographic and clinical characteristics were collected for subgroup analyses. A total of 747 patients were registered. Successful EGFR mutation analysis was performed in 741, with an overall mutation rate of 50.2%. The EGFR active mutation rate is 48.0% (with 1.3% of combined active and resistance mutations). Tobacco use (>30 pack-year vs. 0–10 pack-year, OR 0.27, 95%CI: 0.17–0.42) and regional lymph nodes involvement (N3 vs. N0, OR 0.47, 95%CI: 0.29–0.76) were independent predictors of EGFR mutation in multivariate analysis. However, even in regular smokers, the EGFR mutation frequency was 35.3%. The EGFR mutation frequency was similar between diverse biopsy sites and techniques. The overall EGFR mutation frequency of the mainland China subset was 50.2%, independently associated with the intensity of tobacco use and regional lymph nodes involvement. The relatively high frequency of EGFR mutations in the mainland China subset suggest that any effort to obtain tissue sample for EGFR mutation testing should be encouraged.

Highlights

  • Lung cancer is the leading cause of cancer-related death in the world [1]

  • Tobacco use (>30 pack-year vs. 0–10 pack-year, OR 0.27, 95% confidence intervals (95%CI): 0.17–0.42) and regional lymph nodes involvement (N3 vs. N0, OR 0.47, 95% CI: 0.29–0.76) were independent predictors of epidermal growth factor receptor (EGFR) mutation in multivariate analysis

  • Several retrospective studies in resectable and advanced lung adenocarcinoma have suggested that gender was not an independent factor for EGFR mutation [10,11]

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Summary

Introduction

Platinum-based chemotherapy remain the main treatment choice for advanced non-small-cell lung cancer (NSCLC) [2]. Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKI) therapy recently achieved promising successes in NSCLC patients harboring EGFR active mutations [3,4,5], significantly prolonging patients’ survival [6,7]. Studies in different populations identified some subgroups (adenocarcinoma histology, women, never-smokers and East Asian ethnic origin) with higher EGFR active mutation rate [8,9]. Several retrospective studies in resectable and advanced lung adenocarcinoma have suggested that gender was not an independent factor for EGFR mutation [10,11]. It is significant to identify demographic and clinical characteristics associated with EGFR mutations, to allow identifying subpopulations of patients at high risk of harboring EGFR mutation, allowing the oncologists to decide which first-line treatment may offer the most benefits

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