PMID- 30032006 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 1936-5233 (Print) IS - 1936-5233 (Electronic) IS - 1936-5233 (Linking) VI - 11 IP - 5 DP - 2018 Oct TI - Efficacy and Safety of Radiotherapy Plus EGFR-TKIs in NSCLC Patients with Brain Metastases: A Meta-Analysis of Published Data. PG - 1119-1127 LID - S1936-5233(18)30195-5 [pii] LID - 10.1016/j.tranon.2018.07.003 [doi] AB - BACKGROUND: The role of radiotherapy (RT) combined with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in non-small cell lung cancer (NSCLC) patients with brain metastasis (BM) remains controversial. Therefore, we conducted a meta-analysis to comprehensively evaluate the efficacy and safety of RT plus EGFR-TKIs in those patients. MATERIALS AND METHODS: Relevant literatures published between 2012 and 2017 were searched. Objective response rate(ORR), disease control rate (DCR), overall survival (OS), intracranial progression-free survival (I-PFS) and adverse events (AEs) were extracted. The combined hazard ratios (HRs) and relative risks (RRs) were calculated using random effects models. RESULTS: Twenty-four studies (2810 patients) were included in the analysis. Overall, RT plus EGFR-TKIs had higher ORR (RR = 1.32, 95%CI: 1.13-1.55), DCR (RR = 1.12, 95%CI: 1.04-1.22), and longer OS (HR = 0.72, 95%CI: 0.59-0.89), I-PFS (HR = 0.64, 95%CI: 0.50-0.82) than monotherapy, although with higher overall AEs (20.2% vs 11.8%, RR = 1.34, 95% CI: 1.11-1.62). Furthermore, subgroup analyses found concurrent RT plus EGFR-TKIs could prolong OS (HR = 0.69, 95%CI: 0.55-0.86) and I-PFS (HR = 0.57, 95%CI: 0.44-0.75). Asian ethnicity and lung adenocarcinoma (LAC) patients predicted a more favorable prognosis (HR = 0.69,95%CI: 0.54-0.88, HR = 0.66, 95%CI: 0.53-0.83, respectively). CONCLUSION: RT plus EGFR-TKIs had higher response rate, longer OS and I-PFS than monotherapy in NSCLC patients with BM. Asian LAC patients with EGFR mutation had a better prognosis with concurrent treatment. The AEs of RT plus EGFR-TKIs were tolerated. CI - Copyright (c) 2018 The Authors. Published by Elsevier Inc. All rights reserved. FAU - Wang, Xueyan AU - Wang X AD - Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, 210029, China. FAU - Xu, Ye AU - Xu Y AD - Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, 210029, China. FAU - Tang, Weiqing AU - Tang W AD - Division of Surgery, Guilin Medical University, Guilin, Guangxi, 541000, China. FAU - Liu, Lingxiang AU - Liu L AD - Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, 210029, China. Electronic address: llxlau@163.com. LA - eng PT - Journal Article PT - Review DEP - 20180720 PL - United States TA - Transl Oncol JT - Translational oncology JID - 101472619 PMC - PMC6074003 EDAT- 2018/07/23 06:00 MHDA- 2018/07/23 06:01 PMCR- 2018/07/20 CRDT- 2018/07/23 06:00 PHST- 2018/05/08 00:00 [received] PHST- 2018/06/29 00:00 [revised] PHST- 2018/07/02 00:00 [accepted] PHST- 2018/07/23 06:00 [pubmed] PHST- 2018/07/23 06:01 [medline] PHST- 2018/07/23 06:00 [entrez] PHST- 2018/07/20 00:00 [pmc-release] AID - S1936-5233(18)30195-5 [pii] AID - 10.1016/j.tranon.2018.07.003 [doi] PST - ppublish SO - Transl Oncol. 2018 Oct;11(5):1119-1127. doi: 10.1016/j.tranon.2018.07.003. Epub 2018 Jul 20.