Abstract

Background: Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) is revolutionizing the management of brain metastases (BMs). This study was to explore the value of upfront cranial radiotherapy (RT) in EGFR-mutated non-small cell lung cancer (NSCLC) with BMs compared with EGFR-TKIs alone.Methods: We searched all topic-related comparative articles in public databases (MEDLINE, EMBASE, Cochrane Library, and Web of Science) and conference proceedings. Outcomes of interest were intracranial objective response rate (ORR), overall survival (OS), and intracranial progression-free survival (PFS). Statistical analyses were calculated using Review Manager 5.3 software.Results: Thirteen comparative studies that included a total of 1,456 patients were eligible. Upfront brain RT had significantly higher OS (HR = 0.78, 95% CI = 0.65–0.93, P = 0.005) than EGFR-TKI alone. Upfront RT plus TKI had superior OS (HR = 0.71, 95% CI = 0.58–0.86, P = 0.0005) and intracranial PFS (HR = 0.69, 95% CI = 0.49–0.99, P = 0.04). The pooled data favored upfront whole brain RT (WBRT) plus TKI in terms of intracranial PFS (HR = 0.64, 95% CI = 0.48–0.85, P = 0.002) and OS (HR = 0.75, 95% CI = 0.57–1, P = 0.05). Upfront stereotactic radiosurgery (SRS) was associated with better OS (HR = 0.37, 95% CI = 0.26–0.54, P < 0.00001). Similar results were observed when analysis was restricted to the use of erlotinib or geftinib.Conclusions: The upfront use of brain RT seemed critical, especially for SRS. Upfront administration of upfront WBRT plus EGFR-TKI had better survival outcomes and seemed superior to EGFR-TKI alone.

Highlights

  • 25 to 40% of all non-small-cell lung cancer (NSCLC) patients will develop brain metastases (BMs) during their disease course, and the risk is even higher in patients with epidermal growth factor receptor (EGFR) mutation (1)

  • The literature selection process is presented in the PRISMA flow chart (Figure 1) according to the PRISMA guidelines

  • A total of 1,456 patients with BMs originated from EGFR-mutated NSCLC in the included studies

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Summary

Introduction

25 to 40% of all non-small-cell lung cancer (NSCLC) patients will develop brain metastases (BMs) during their disease course, and the risk is even higher in patients with epidermal growth factor receptor (EGFR) mutation (1). EGFR tyrosine kinase inhibitors (EGFR-TKIs) have been integrated into the treatment algorithm of advanced metastatic EGFR-mutated NSCLC as first-line therapy, because of better response and survival rates compared with conventional chemotherapy (4). For EGFR-mutated NSCLC patients with newly developed BMs, it’s of great interest to know whether the time of brain RT could be delayed after TKI administration alone to avoid the serious neurological side effects. Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) is revolutionizing the management of brain metastases (BMs). This study was to explore the value of upfront cranial radiotherapy (RT) in EGFR-mutated non-small cell lung cancer (NSCLC) with BMs compared with EGFR-TKIs alone

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