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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Efficacy of epidermal growth factor receptor tyrosine kinase inhibitors for brain metastasis in non-small cell lung cancer patients harboring either exon 19 or 21 mutation
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Efficacy of epidermal growth factor receptor tyrosine kinase inhibitors for brain metastasis in non-small cell lung cancer patients harboring either exon 19 or 21 mutation

机译:表皮生长因子受体酪氨酸激酶抑制剂对具有外显子19或21外显子突变的非小细胞肺癌患者脑转移的疗效

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摘要

Non-small cell lung cancer (NSCLC) harboring an activating epidermal growth factor receptor (EGFR) mutation shows good and rapid response to EGFR tyrosine kinase inhibitors (TKIs). We prospectively evaluated the efficacy of EGFR TKI for metastatic brain tumors in NSCLC patients harboring EGFR mutation. This was an open-label, single-institution, phase II study. Patients diagnosed with NSCLC harboring EGFR mutation and measurable metastatic brain tumors were eligible. They received either erlotinib or gefitinib once a day. Out of total 28 patients enrolled, 23 patients (83%) showed a partial response (PR) and 3 patients (11%) did stable disease (SD), giving a disease control rate of 93%. Median progression free survival (PFS) and overall survival (OS) were 6.6 months (95% CI, 3.8-9.3 months) and 15.9 months (95% CI, 7.2-24.6 months), respectively. There was no difference in PFS and OS according to EGFR TKIs used. After discontinuation of the treatment, 14 patients (50%) received local therapy for metastatic brain tumors during their disease course, either whole brain radiotherapy or radiosurgery, giving a local therapy-free interval of 12.6 months (95% CI, 7.6-17.6 months). EGFR TKI therapy might be the treatment of choice for metastatic brain tumors in NSCLC patients harboring an activating EGFR mutation.
机译:具有活化表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)对EGFR酪氨酸激酶抑制剂(TKIs)表现出良好而快速的反应。我们前瞻性评估了EGFR TKI对具有EGFR突变的NSCLC患者转移性脑肿瘤的疗效。这是一个开放性,单一机构的II期研究。被诊断患有EGFR突变和可测量的转移性脑肿瘤的NSCLC患者符合条件。他们每天接受一次厄洛替尼或吉非替尼治疗。在入组的28位患者中,有23位患者(83%)表现出部分反应(PR),而3位患者(11%)表现出稳定疾病(SD),疾病控制率为93%。中位无进展生存期(PFS)和总体生存期(OS)分别为6.6个月(95%CI,3.8-9.3个月)和15.9个月(95%CI,7.2-24.6个月)。根据所使用的EGFR TKI,PFS和OS没有差异。停止治疗后,有14位患者(50%)在其病程中接受了局部治疗,即全脑放疗或放射外科手术治疗转移性脑瘤,无局部治疗的间隔时间为12.6个月(95%CI,7.6-17.6个月) )。 EGFR TKI治疗可能是具有激活性EGFR突变的NSCLC患者转移性脑肿瘤的治疗选择。

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