期刊文献+

非小细胞肺癌中EML4-ALK融合基因的检测及临床意义 被引量:5

Detection and Clinical Significance of ALK Fusion Gene in Non-small Cell Lung Cancer
下载PDF
导出
摘要 目的:为了对非小细胞肺癌的治疗提供参考依据,分析ALK融合基因的检测及临床意义。方法:根据随机原则的相关要求从2015年1月-2018年6月在笔者所在医院治疗的非小细胞肺癌患者中抽取60例作为研究对象,所有患者均通过二代测序技术(NGS)检测病理标本中的EML4-ALK融合基因,探讨EML4-ALK融合基因表达与各病理特征及临床指标的关系。结果:研究数据显示,60例患者中EML4-ALK融合基因阳性表达率为13.33%(8/60),而且阳性表达率在病理组织类型、既往吸烟史及肿瘤分化程度间比较差异有统计学意义(P<0.05)。结论:在非小细胞肺癌患者中EML4-ALK融合基因存在过度表达的情况,这与肿瘤的发生、发展密切相关,临床应重视对其检测。 Objective:To provide reference for the treatment of non-small cell lung cancer,and to analyze the detection and clinical significance of EML4-ALK fusion gene.Method:According to the relevant requirements of random principle,60 patients with non-small cell lung cancer treated in our hospital from January 2015 to June 2018 were selected as the research subjects.All patients were detected ALK fusion gene in pathological specimens by second generation sequencing(NGS),and the relationship between ALK fusion gene expression and pathological characteristics and clinical indicators was discussed.Result:The data showed that the positive expression rate of ALK fusion gene was 13.33%(8/60) in 60 patients,and there were significant differences in histopathological type,smoking history and tumor differentiation(P<0.05).Conclusion:Overexpression of ALK fusion gene exists in NSCLC patients,which is closely related to the occurrence and development of tumors.Clinical detection of ALK fusion gene shall be emphasized.
作者 邓婉芳 罗承东 邢世江 黄丽云 曾维斌 李新 许家健 DENG Wanfang;LUO Chengdong;XING Shijiang(Zhongshan Xiaolan People’s Hospital,Zhongshan 528415,China)
出处 《中外医学研究》 2019年第11期63-65,共3页 CHINESE AND FOREIGN MEDICAL RESEARCH
关键词 非小细胞肺癌 EML4-ALK融合基因 肿瘤 Non-small cell lung cancer ALK fusion gene Tumor
  • 相关文献

参考文献11

二级参考文献242

  • 1苗普生.塔里木盆地边缘地区的民族融合和维吾尔族的形成与发展[J].西域研究,2005(4):1-8. 被引量:19
  • 2Daniel C. Lung cancer, a worrying epidemiological evolution [J]. Rev Infirm, 2012, 8(184): 14.
  • 3Chu D T, Kim S W, Hsu H K, et al. Patient attitudes to- wards chemotherapy and survival: a prospective observational study in advanced non- small cell lung cancer[J]. Lung Can- cer, 2009, 66(2): 250.
  • 4Chih- Hsin Y. EGFR tyrosine kinase inhibitors for the treat- ment of NSCLC in East Asia: present and future [ J ]. Lung Cancer, 2008, 60(2): 23.
  • 5Linardou H, Dahabreh I J, Kana loupiti D, et al. Assess- ment of somatic kras mutations as a mechanism associated with resistance to EGFR- targe ted agents: a systematic re- view and meta- analysis of studies in advanced non - small - cell lung cancer and metastatic colorectal cancer[J ]. Lancet Oncol, 2008, 9(10): 962.
  • 6Scagliotti G V, Selvaggi G, Novello S, et al. The biology of epidermal growth factor receptor in lung cancer [ J ]. Clin Cancer Re.s, 2004, 10(12): 4227.
  • 7Antonieelli A, Cafarotti S, Indini A, et al. EGFR - targeted therapy for non - small cell lung cancer: focus on EGFR oncogenie mutation[J]. Int J Med Sci, 2013, 10(3) : 320.
  • 8Maemondo M, Inoue A, Kobayashi K, et al. Gefltinib or chemotherapy for non- small - cell lung cancer with mutated EGFR[J]. N Engl J Med, 2010, 362(25) : 2380.
  • 9Zhou C, Wu Y- L, Chen G, et al. Erlotinib versus chemotherapy as first - line treatment for patients with ad- vanced EGFR mutation - positive non- small cell lung cancer (OPTIMAL, CTONG - 0802 ) : a multicentre, open - la- bel, randomised, phase 3 study[J]. Lancet Oncol, 2011, 12 (8) : 735.
  • 10Lam K C, Mok T S. Targeted therapy: an evolving world of lung cancer[J]. Respirology, 2011, 16(1): 13.

共引文献71

同被引文献55

引证文献5

二级引证文献13

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