期刊文献+

EML4-ALK融合基因阳性肺腺癌合并淋巴瘤1例并文献复习 被引量:1

A Case Report: an EML4-ALK Positive Lung Adenocarcinoma Diagnosed with Lymphoma Previously
下载PDF
导出
摘要 近年来随着分子生物学研究的不断深入,靶向治疗成为当前肺癌治疗的趋势。目前肺癌个体化的最佳治疗效果日益受到重视,棘皮动物微管相关蛋白4-间变型淋巴瘤激酶(echinoderm microtubule associated protein like4 anaplastic lymphoma kinase,EML4-ALK)融合基因作为新兴生物标记物是当前肺癌治疗领域研究热点。与此同时,随着抗肿瘤治疗水平的不断提高,生存期明显延长,发生多原发癌(multiple primary carcinomas,MPC)的机会增多。EML4-ALK融合基因阳性的肺腺癌合并淋巴瘤发生于同一患者文献报道罕见。本文报道1例ALK融合基因阳性的非小细胞肺癌(non-small cell lung cancer,NSCLC)合并淋巴瘤病例,同时对异时性肺癌合并淋巴瘤的文献进行复习。 In recent years, with the deepening of the research of molecular biology, targeted therapy has become one of the trend of lung cancer treatment. hTe individualized treatment of lung cancer is attached great importance at present. Echinoderm microtubule associated protein like 4 anaplastic lymphoma kinase (EML4-ALK) as a new biological marker is a hot topic in the ifeld of lung cancer treatment. Meanwhile, with the improvement of anticancer treatment and survival, the inci-dence of multiple primary carcinomas (MPC) has become increasingly. But the report that malignant lymphoma complicated with lung adenocarcinoma harboring EML4-ALK fusion gene in one individual is rare. Here, we report an EML4-ALK positive non-small cell lung cancer (NSCLC) in a patient previously diagnosed with T cell lymphoma and review literature on meta-chronous lung cancer complicating with lymphoma.
作者 刘丽 衡伟
出处 《中国肺癌杂志》 CAS CSCD 北大核心 2015年第2期89-91,共3页 Chinese Journal of Lung Cancer
基金 国家临床重点专科建设项目资助~~
关键词 肺肿瘤 淋巴瘤 治疗 第二原发癌 间变性淋巴瘤激酶 Lung neoplasms Lymphoma Treatment Second primary carcinoma Anaplastic lymphoma kinase
  • 相关文献

参考文献11

  • 1Noh SK, Yoon JY, Ryoo UN, et al. A case report of quadruple cancer in a single patient including the breast, rectum, ovary, and endometrium. J Gynecol Oncol, 2008,19(4): 265-269.
  • 2Watanabe S, Harris C. Multiple primary cancer: the U.S.-Japan Cooperative Cancer Research Program. JpnJ Cancer Res, 1990,81(2): 201-205.
  • 3Konits PH, Aisner J, Whitacre M, et al. Lung cancer as a complication of prolonged survival in patients with lymphoma. Med Pediatr Oncol, 1982, 10(4): 331-338.
  • 4Van Leeuwen FE, Somers R, Taal BG, et al. Increased risk of lung cancer, non-Hodgkin^ lymphoma, and leukemia following Hodgkin’s disease. J Clin Oncol, 1989,7(8): 1046-1058.
  • 5Travis LB, Curtis RE; Boice JD, et al. Second cancers following non-Hodgkin's lymphoma. Cancer, 1991,67(7): 2002-2009.
  • 6Lorenzo Bermejo J, Pukkala E, Johannesen TB, et al. Age-time risk patterns of solid cancers in 60,901 non-Hodgkin lymphoma survivors from Finland, Norway and Sweden. BrJ Haematol, 2014,164(5): 675-683.
  • 7Soda M, Choi YL, Enomoto M, et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature, 2007, 448(7153):561-566.
  • 8Garber IC ALK, lung cancer, and personalized therapy: portent of the future ? J Nad Cancer Inst, 2010,102(10): 672-675.
  • 9Shaw AT, Kim DW, Nakagawa K, et al. Crizotinib versus chemotherapy in advanced ALK-positive lung cancer. N EnglJ Med, 2013, 368(25): 2385-2394.
  • 10Steuer CE, Ramalingam SS. ALK-positive non-small cell lung cancer: Mechanisms of resistance and emerging treatment options. Cancer, 2014, 120(16):2392-2402.

同被引文献2

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部