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表皮生长因子受体突变型非小细胞肺癌伴脑转移的治疗效果和安全性:多变量生存分析的循证贝叶斯网络荟萃研究。

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.

机构信息

Departments of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.

出版信息

Aging (Albany NY). 2020 Jul 15;12(14):14244-14270. doi: 10.18632/aging.103455.

Abstract

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.

摘要

表皮生长因子受体 (EGFR)-突变型非小细胞肺癌 (NSCLC) 伴脑转移的优选治疗方法仍难以确定。本研究旨在评估系统治疗的相对疗效和安全性。确定了关于 EGFR 突变型、脑转移 NSCLC 的治疗的临床试验。使用随机效应贝叶斯网络荟萃分析 (NMA) 对风险比 (HR) 尺度进行无进展生存期 (PFS) 和总生存期 (OS) 分析。根据临床或个体因素的列线图和 Kaplan-Meier 图是使用从监测、流行病学和最终结果 (SEER) 数据库中获得的数据显示的。第三代 EGFR-酪氨酸激酶抑制剂 (EGFR-TKI)(奥希替尼)、EGFR-TKI+立体定向放射外科 (SRS)/全脑放疗 (WBRT)(吉非替尼/厄洛替尼+SRS/WBRT)和 EGFR-TKI(厄洛替尼)+抗血管内皮生长因子受体 (抗-VEGFR)(贝伐珠单抗)可获得更好的 PFS(HR:0.30[0.15-0.59];HR:0.47[0.31-0.72];HR:0.50[0.21-1.21] 与延迟 SRS/WBRT 相比)和可接受性;EGFR-TKI+SRS/WBRT 在 OS 方面排名最高(与其他相比),其次是第三代 EGFR-TKI。在 1173 例脑转移 NSCLC 患者的数据集队列中,6 个月、1 年和 3 年的生存率分别为 59.8%、41.3%和 5.6%。种族和起源以及诊断年份是 OS 的独立预测因素。生存曲线表明,OS 因组织学和种族而异。第三代 EGFR-TKI 和 EGFR-TKIs+SRS/WBRT 对平衡 OS 和 PFS 的 EGFR 突变型 NSCLC 伴脑转移更有效且潜在可接受。没有辅助治疗的手术不能显著提高脑转移 NSCLC 患者的 OS。该研究强调了奥希替尼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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