Departments of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Aging (Albany NY). 2020 Jul 15;12(14):14244-14270. doi: 10.18632/aging.103455.
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.
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。