埃罗替尼                        
                
                                
                        
                            肺癌                        
                
                                
                        
                            脑转移                        
                
                                
                        
                            表皮生长因子受体                        
                
                                
                        
                            肿瘤科                        
                
                                
                        
                            奥西默替尼                        
                
                                
                        
                            医学                        
                
                                
                        
                            吉非替尼                        
                
                                
                        
                            危险系数                        
                
                                
                        
                            内科学                        
                
                                
                        
                            贝伐单抗                        
                
                                
                        
                            转移                        
                
                                
                        
                            癌症                        
                
                                
                        
                            化疗                        
                
                                
                        
                            置信区间                        
                
                        
                    
            作者
            
                Binghao Zhao,Yuekun Wang,Yaning Wang,Wenlin Chen,Lizhou Zhou,Peng Hao Liu,Ziren Kong,Congxin Dai,Yu Wang,Wenbin Ma            
         
                    
            出处
            
                                    期刊:Aging
                                                         [Impact Journals LLC]
                                                        日期:2020-07-15
                                                        卷期号:12 (14): 14244-14270
                                                        被引量:30
                                 
         
        
    
            
            标识
            
                                    DOI:10.18632/aging.103455
                                    
                                
                                 
         
        
                
            摘要
            
            Preferable treatments for epidermal growth factor receptor (EGFR)-mutant non-small cell lung cancer (NSCLC) with brain metastasis are elusive. The study intended to estimate the relative efficacy and safety of systemic therapies. Clinical trials about therapies for EGFR-mutant, brain-metastatic NSCLC were identified. Progression-free survival (PFS) and overall survival (OS) were analysed using random effects Bayesian network meta-analyses (NMAs) on the hazard ratio (HR)-scale. Nomogram and Kaplan-Meier plots based on clinical or individual factors are displayed using data obtained from the Surveillance Epidemiology and End Results (SEER) database. Third-generation EGFR- tyrosine kinase inhibitors (EGFR-TKI) (osimertinib), EGFR-TKIs + stereotactic radiosurgery (SRS)/whole brain radiotherapy (WBRT) (gefitinib/erlotinib + SRS/WBRT), and EGFR-TKIs (erlotinib) + anti-vascular endothelial growth factor receptor (anti-VEGFR) (bevacizumab) achieved superior PFS (HR: 0.30 (0.15-0.59); HR: 0.47 (0.31-0.72); HR: 0.50 (0.21-1.21) vs. deferring SRS/WBRT) and acceptability; EGFR-TKIs + SRS/WBRT was top ranking (vs. others) for OS followed by third-generation EGFR-TKI. In the dataset cohort of 1173 brain-metastatic NSCLC patients, the 6-month, 1-year, and 3-year survival rates were 59.8%, 41.3%, and 5.6%, respectively. Race and origin, and year of diagnosis were independent predictors of OS. Survival curves showed that the OS of patients varied significantly by histology and race. Third-generation EGFR-TKI and EGFR-TKIs + SRS/WBRT are more effective and potentially acceptable for EGFR-mutant NSCLC with brain metastases balancing OS and PFS. Surgeries without adjuvant therapies cannot significantly improve the OS of brain-metastatic NSCLC patients. The study highlights importance of osimertinib in these patients and provide a reference for clinical treatments.
         
            
 
                 
                
                    
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