中国癌症杂志 ›› 2015, Vol. 25 ›› Issue (6): 468-472.doi: 10.3969/j.issn.1007-3969.2015.06.010

• 论著 • 上一篇    下一篇

克唑替尼治疗ALK阳性非小细胞肺癌脑转移的疗效观察

黄伟,王琳,秦叔逵,杨宁蓉,李嵘,寻琛,夏兆君   

  1. 解放军八一医院全军肿瘤中心肿瘤内科,江苏 南京 210002
  • 出版日期:2015-06-30 发布日期:2015-08-14
  • 通信作者: 王琳 E-mail:wanglin81yy@163.com

Efficacy analysis of crizotinib for brain metastases in ALK-rearrangement-positive non-small cell lung cancer

HUANG Wei, WANG Lin, QIN Shukui, YANG Ningrong, LI Rong, XUN Chen, XIA Zhaojun   

  1. Department of Medical Oncology, Cancer Center of PLA, 81 Hospital of PLA, Nanjing Jiangsu 210002, China
  • Published:2015-06-30 Online:2015-08-14
  • Contact: WANG Lin E-mail: wanglin81yy@163.com

摘要:      背景与目的:克唑替尼对间变性淋巴瘤激酶(anaplastic lymphoma kinase,ALK)阳性非小细胞肺癌(non-small cell lung cancer,NSCLC)具有显著疗效,但在治疗中往往出现脑转移,本研究旨在探讨克唑替尼在ALK阳性NSCLC脑转移患者中的治疗疗效和治疗模式。方法:对2011年1月—2014年8月在解放军八一医院接受克唑替尼治疗的6例ALK阳性NSCLC脑转移患者的临床资料进行回顾性分析。结果:3例克唑替尼治疗前基线有脑转移患者,颅内疗效部分缓解(partial response,PR)1例、疾病稳定(stable disease,SD)2例;第1次服用克唑替尼治疗至第1次出现疾病进展(progressive disease,PD)的中位时间为5.7个月,且第1次疾病进展的部位均为脑。6例患者脑病灶进展接受放疗后继续服用克唑替尼治疗,中位无进展生存期(progression free survival,PFS)为4.0个月,其中1例患者继续接受克唑替尼治疗的PFS达23.3个月,颅内病灶疗效完全缓解(complete response,CR)。结论:克唑替尼治疗ALK阳性NSCLC脑转移患者有效,且对于单纯颅内病灶进展放疗后,继续接受克唑替尼治疗仍然有效,是临床上可以选择的治疗方式。

关键词: 非小细胞肺癌, 脑转移, 间变性淋巴瘤激酶, 克唑替尼

Abstract:        Background and purpose: Although crizotinib could manifest marked antitumor activity in anaplastic lymphoma kinase (ALK)-rearrangement-positive non-small cell lung cancer (NSCLC) patients, but brain metastases is always occured in such patients. This study aimed to explore the efficacy and treatment mode of crizotinib for brain metastases in ALK-rearrangement-positive NSCLC. Methods: The clinical data of 6 patients with brain metastases in ALK-rearrangement-positive NSCLC treated in 81 Hospital of PLA from Jan. 2011 to Aug. 2014 were analyzed retrospectively. Results: Three patients had brain metastases before crizotinib administration, 1 obtained partial response (PR) and 2 obtained stable disease (SD) in intracraninal tumors. The median progression free survival (PFS)for the first period of crizotinib administration were 5.7 months, and the sites of first disease progression were brains. All the 6 patients continued to receive crizotinib after radiotherapy with the median PFS of 4 months. One patient even experienced a median PFS of 23.3 months for the second period of crizotinib administration, and her brain tumors obtained complete response (CR). Conclusion: The data of this study suggest that crizotinib is effective for brain metastases in ALK-rearrangement-positive NSCLC, and continued administration of crizotinib after radiotherapy for isolated intracraninal tumor progression is a elective treatment option for such patients.

Key words: Non-small cell lung cancer, Brain metastases, Anaplastic lymphoma kinase, Crizotinib