Lin Chia-Ying, Chang Chao-Chun, Su Po-Lan, Lin Chien-Chung, Tseng Yau-Lin, Su Wu-Chou, Yen Yi-Ting
Department of Medical Imaging.
Division of Thoracic Surgery, Department of Surgery, National Cheng Kung University Hospital, College of Medical College, National Cheng Kung University.
Medicine (Baltimore). 2019 Aug;98(33):e16766. doi: 10.1097/MD.0000000000016766.
Patients with non-small cell lung cancer (NSCLC) and de novo brain metastasis (BM) have poor prognosis. We aim to investigate the characteristic of brain magnetic resonance (MR) imaging and the association with the treatment response of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) for lung cancer with BM.EGFR-mutated NSCLC patients with BM from October 2013 to December 2017 in a tertiary referral center were retrospectively analyzed. Patient's age, sex, cell type, EGFR mutation status, treatment, and characteristics of BM were collected. Survival analysis was performed using Kaplan-Meier method. The efficacy of different EGFR-TKIs were also analyzed.Among the 257 eligible patients, 144 patients with Exon 19 deletion or Exon 21 L858R were included for analysis. The erlotinib group had the best progression free survival (PFS) (median PFS 13 months, P = .04). The overall survival (OS) revealed no significant difference between three EGFR-TKI groups. Brain MR imaging features including tumor necrosis, rim enhancement and specific tumor locations (frontal lobe, putamen or cerebellum) were factors associated with poor prognosis. Patients with poor prognostic imaging features, the high-risk group, who received erlotinib had the best PFS (median PFS 12 months, P < .001). However, the OS revealed no significant difference between 3 EGFR-TKI groups. The low risk group patients had similar PFS and OS treated with three different EGFR-TKIs.In NSCLC patients with common EGFR mutation and de novo BM, those with poor prognostic brain MR characteristics, erlotinib provided better PFS than afatinib or gefitinib.
非小细胞肺癌(NSCLC)合并新发脑转移(BM)的患者预后较差。我们旨在研究脑磁共振(MR)成像特征以及其与表皮生长因子受体-酪氨酸激酶抑制剂(EGFR-TKIs)治疗NSCLC合并BM疗效的相关性。对2013年10月至2017年12月在一家三级转诊中心的EGFR突变的NSCLC合并BM患者进行回顾性分析。收集患者的年龄、性别、细胞类型、EGFR突变状态、治疗情况以及BM的特征。采用Kaplan-Meier法进行生存分析。同时分析不同EGFR-TKIs的疗效。在257例符合条件的患者中,纳入144例存在第19外显子缺失或第21外显子L858R突变的患者进行分析。厄洛替尼组的无进展生存期(PFS)最佳(中位PFS为13个月,P = 0.04)。三个EGFR-TKI组之间的总生存期(OS)无显著差异。脑MR成像特征,包括肿瘤坏死、边缘强化以及特定的肿瘤位置(额叶、壳核或小脑)是预后不良的相关因素。具有不良预后成像特征的高危组患者接受厄洛替尼治疗时PFS最佳(中位PFS为12个月,P < 0.001)。然而,三个EGFR-TKI组之间的OS无显著差异。低危组患者接受三种不同的EGFR-TKIs治疗时PFS和OS相似。在具有常见EGFR突变和新发BM的NSCLC患者中,脑MR特征预后不良者,厄洛替尼较阿法替尼或吉非替尼提供更好的PFS。