Abstract

BackgroundNon-small cell lung cancer (NSCLC) with brain metastasis (BM) harboring an epidermal growth factor receptor (EGFR) mutation shows good response to tyrosine kinase inhibitors (TKIs). This study is to assess the appropriate timing of brain radiotherapy (RT) for asymptomatic BM in EGFR mutant NSCLC patients.MethodsThere were 628 patients diagnosed with EGFR mutant NSCLC between October 2005 and December 2011. Treatment outcomes had been retrospectively evaluated in 96 patients with asymptomatic BM without prior TKI treatment. 39 patients received first-line brain RT, 23 patients received delayed brain RT, and 34 patients did not receive brain RT.ResultsWith a median follow-up of 26 months, the 2-year OS was 40.6 %. Univariate analyses revealed that ECOG performance status (p = 0.006), other distant metastases (p = 0.002) and first line systemic treatment (p = 0.032) were significantly associated with overall survival (OS). Multivariate analyses revealed that other sites of distant metastases (p = 0.030) were prognostic factor. The timing of brain RT was not significantly related to OS (p = 0.246). The 2-year BM progression-free survival (PFS) was 26.9 %. Brain RT as first-line therapy failed to demonstrate a significant association with BM PFS (p = 0.643).ConclusionsFirst-line brain RT failed to improve long-term survival in TKI-naïve EGFR mutant NSCLC patients with asymptomatic BM. Prospective studies are needed to validate these clinical findings.

Highlights

  • Non-small cell lung cancer (NSCLC) with brain metastasis (BM) harboring an epidermal growth factor receptor (EGFR) mutation shows good response to tyrosine kinase inhibitors (TKIs)

  • Epidermal growth factor receptor (EGFR) mutations are associated with a significant sensitivity to EGFR tyrosine kinase inhibitors (TKI), which can significantly improve treatment outcome [4]

  • Several reports demonstrate that NSCLC patients with mutant EGFR and BM could achieve favorable outcomes when treated with EGFR-TKIs as single-agent chemotherapy

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Summary

Introduction

Non-small cell lung cancer (NSCLC) with brain metastasis (BM) harboring an epidermal growth factor receptor (EGFR) mutation shows good response to tyrosine kinase inhibitors (TKIs). Epidermal growth factor receptor (EGFR) mutations are associated with a significant sensitivity to EGFR tyrosine kinase inhibitors (TKI), which can significantly improve treatment outcome [4]. The efficacy of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) for NSCLC patients with BM has been reported [5, 6]. Several studies have reported that TKI treatment results in high response rates (70–89 %) and increased overall survival (OS) and progression-free survival (PFS) (12.9–19.8 months and 6.6–23.3 months, respectively) in selected populations of EGFR-mutated NSCLC patients with BM [7,8,9]

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