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Efficacy and safety of therapies for EGFR-mutant non-small cell lung cancer with brain metastasis: an evidence-based Bayesian network pooled study of multivariable survival analyses

机译:具有脑转移的EGFR-突变体非小细胞肺癌疗法的疗效和安全性:基于证据的贝叶斯网络汇总的多变量存活分析研究

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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.
机译:具有脑转移的表皮生长因子受体(EGFR) - 富含非小细胞肺癌(NSCLC)的优选治疗是难以捉摸的。该研究旨在估算系统疗法的相对功效和安全性。鉴定了关于EGFR-突变体,脑 - 转移NSCLC疗法的临床试验。使用随机效应贝叶斯网络元分析(NMA)对危险比(HR)-Scale进行无规效应的无进展生存(PFS)和总存活(OS)。使用从监视流行病学和最终结果(SEER)数据库中获得的数据来显示基于临床或个人因素的NOM图和KAPLAN-MEIER图。第三代EGFR-酪氨酸激酶抑制剂(EGFR-TKI)(OSIMERTINIB),EGFR-TKIS +立体定向放射牢(SRS)/全脑放射治疗(WBRT)(GEFITINIB / ERLOTINIB + SRS / WBRT),以及EGFR-TKIS(ERLOTINIB) +抗血管内皮生长因子受体(抗VEGFR)(Bevacizumab)达到优异的PFS(HR:0.30(0.15-0.59); HR:0.47(0.31-0.72); HR:0.50(0.21-1.21)与推迟SRS / WBRT)和可接受性; EGFR-TKIS + SRS / WBRT是OS的顶部排名(与其他人),然后是第三代EGFR-TKI。在1173名脑转移性NSCLC患者的数据集队列中,6个月,1年和3年生存率分别为59.8%,41.3%和5.6%。种族和起源以及诊断年份是OS的独立预测因子。存活曲线表明,患者的操作系统通过组织学和种族显着变化。第三代EGFR-TKI和EGFR-TKIS + SRS / WBRT对于具有脑转移平衡OS和PFS的EGFR-突变体NSCLC更有效,并且可能是可接受的。没有佐剂疗法的手术不能显着改善脑 - 转移NSCLC患者的OS。该研究突出了Osimertinib在这些患者中的重要性,并为临床治疗提供了参考。

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