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表皮生长因子受体酪氨酸激酶抑制剂对携带外显子 19 或 21 突变的非小细胞肺癌脑转移患者的疗效。

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.

机构信息

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43-gil, Songpa-gu, Seoul 138-736, Republic of Korea.

出版信息

Lung Cancer. 2012 Sep;77(3):556-60. doi: 10.1016/j.lungcan.2012.05.092. Epub 2012 Jun 5.

DOI:10.1016/j.lungcan.2012.05.092
PMID:22677429
Abstract

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.

摘要

非小细胞肺癌(NSCLC)中存在激活的表皮生长因子受体(EGFR)突变对 EGFR 酪氨酸激酶抑制剂(TKI)具有良好且快速的反应。我们前瞻性地评估了 EGFR TKI 对 NSCLC 患者中存在 EGFR 突变的转移性脑肿瘤的疗效。这是一项开放标签、单机构、二期研究。符合条件的患者为诊断为 NSCLC 且存在可测量的转移性脑肿瘤、携带 EGFR 突变的患者。他们每天接受厄洛替尼或吉非替尼治疗。在总共入组的 28 名患者中,23 名(83%)患者表现出部分缓解(PR),3 名(11%)患者表现出疾病稳定(SD),疾病控制率为 93%。中位无进展生存期(PFS)和总生存期(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)。根据使用的 EGFR TKI,PFS 和 OS 没有差异。治疗停止后,14 名患者(50%)在疾病过程中接受了转移性脑肿瘤的局部治疗,全脑放疗或立体定向放疗,局部治疗无进展间隔为 12.6 个月(95%CI,7.6-17.6 个月)。对于携带激活型 EGFR 突变的 NSCLC 患者的转移性脑肿瘤,EGFR TKI 治疗可能是首选治疗方法。

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