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The effectiveness of EGFR-TKIs against brain metastases in EGFR mutation-positive non-small-cell lung cancer

机译:EGFR-TKIs对抗EGFR突变阳性非小细胞肺癌脑转移的有效性

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摘要

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 EGFR mutation. A total of 148 patients with brain metastases from EGFR 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 EGFR mutation and might be the treatment choice in this clinical setting.
机译:非小细胞肺癌(NSCLC)的脑转移是常见的,预后较差,可用的治疗选择很少。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)对具有激活性EGFR突变的非小细胞肺癌脑转移的疗效。回顾性分析了148例EGFR突变阳性NSCLC引起的脑转移患者。每天口服一次吉非替尼(250 mg)或厄洛替尼(150 mg),直至颅内疾病进展,死亡或无法忍受的副作用。使用Kaplan-Meier分析和对数秩检验进行生存分析。脑病变内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)和总体生存期(OS)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无统计学相关性。 EGFR-TKIs在激活EGFR突变的NSCLC患者中显示出对脑转移的有希望的抗肿瘤活性,可能是这种临床治疗的选择。

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