Bai Hao, Xiong Liwen, Han Baohui
Department of Respiratory Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.
Onco Targets Ther. 2017 Apr 27;10:2335-2340. doi: 10.2147/OTT.S129809. eCollection 2017.
Brain metastases are usual in non-small-cell lung cancer (NSCLC) with poor prognosis and few available therapeutic options. This retrospective study aims to evaluate the efficacy of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) against brain metastases from NSCLC harboring activating mutation. A total of 148 patients with brain metastases from mutation-positive NSCLC were analyzed retrospectively. The patients were orally given gefitinib (250 mg) or erlotinib (150 mg) once a day until intracranial disease progression, death, or intolerable side effects. A survival analysis was done using the Kaplan-Meier analysis and log-rank test. Objective response rate and disease control rate within brain lesions were 36.5% and 87.2%, respectively, with a median progression-free survival (PFS) and overall survival (OS) of 11.2 months (95% confidence interval [CI], 10.1-12.3) and 13.6 months (95% CI, 12.3-14.9), respectively. The patients' characteristics were not statistically associated with PFS and OS. EGFR-TKIs showed promising antitumor activity against brain metastases in NSCLC patients with activating mutation and might be the treatment choice in this clinical setting.
脑转移在非小细胞肺癌(NSCLC)中很常见,预后较差且可用的治疗选择有限。这项回顾性研究旨在评估表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)对携带激活突变的NSCLC脑转移瘤的疗效。对总共148例来自突变阳性NSCLC的脑转移患者进行了回顾性分析。患者每天口服吉非替尼(250 mg)或厄洛替尼(150 mg)一次,直至颅内疾病进展、死亡或出现无法耐受的副作用。使用Kaplan-Meier分析和对数秩检验进行生存分析。脑内病变的客观缓解率和疾病控制率分别为36.5%和87.2%,中位无进展生存期(PFS)和总生存期(OS)分别为11.2个月(95%置信区间[CI],10.1 - 12.3)和13.6个月(95%CI,12.3 - 14.9)。患者的特征与PFS和OS无统计学关联。EGFR-TKIs对携带激活突变的NSCLC脑转移瘤显示出有前景的抗肿瘤活性,可能是这种临床情况下的治疗选择。