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作 者:吕嘉林[1] 张权[1] 秦娜[1] 杨新杰[1] 张新勇[1] 吴羽华[1] 李曦[1] 张卉[1] 王敬慧[1] 张树才[1]
机构地区:[1]首都医科大学附属北京胸科医院肿瘤内科,北京市结核病胸部肿瘤研究所,北京101149
出 处:《结核病与胸部肿瘤》2016年第4期250-255,共6页Tuberculosis and Thoracic Tumor
摘 要:背景与目的间变性淋巴瘤激酶(anaplasticlymphomakinase,ALK)阳性非小细胞肺癌(non—smallcelllungcancer,NSCLC)是肺癌的一个重要亚型。ALK阳性NSCLC脑转移患者的治疗尚无标准模式。方法本研究对我院2013年3月-2016年3月期间确诊的ALK阳性NSCLC脑转移患者的临床资料和治疗情况进行回顾性分析,探讨不同治疗模式患者的转归。结果84例晚期ALK阳性NSCLC患者中,22例初诊时有脑转移,剔除3例合并表皮生长因子受体(epidermalgrowthfactorreceptor,EGFR)双突变患者,共19例纳入分析。中位颅内疾病进展时间(progression.freesurvival,PFS)为12.0个月,一线脑部局部治疗(P=0.021)及一线克唑替尼治疗(P=-0.030)可延长PFS;一线克唑替尼联合脑部局部治疗的中位颅内PFS为27.0个月,而单纯克唑替尼治疗的PFS仅为4.2个月。结论一线克唑替尼联合脑部局部治疗有助于延长ALK阳性晚期NSCLC患者的颅内PFS,因例数少,尚有待大样本多中心前瞻性临床研究证实。Background and objective Anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC) is an important subtype of lung cancer. The standard modality ofALK-positive NSCLC with brain metastases remains uncertain. Methods We collected data on clinical characteristics and treatment of patients with ALK-positive NSCLC and brain metastases between March 2013 and March 2016 and retrospectively analyzed patient outcomes. Results In 84 ALK-positive patients with advanced NSCLC, 22 (26.2%) had brain metastases during the initial diagnosis of lung cancer, among which 3 patients with EGFR mutation were excluded, and 19 patients were analyzed. Median intracranial progression-free survival (PFS) was 12.0 months. PFS for patients who received first-line local brain therapy (P=0.021) and crizotinib therapy (P=-0.030) was superior to PFS for patients without such therapies. PFS for patients who received first-line crizotinib combined with local brain therapy was 27.0 months and only 4.2 months for those who received crizotinib alone. Conclusion First-line crizotinib therapy combined with local brain treatment can improve intracranial PFS for ALK-positive NSCLC with brain metastases. This finding should be confirmed further through multicenter, prospective clinical trials with large sample size.
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