期刊文献+

嘉兴地区102例非小细胞肺癌组织标本EGFR基因突变与临床分析

EGFR mutations and clinicopathological features in patients with non-small cell lung cancer
暂未订购
导出
摘要 目的观察嘉兴地区非小细胞肺癌(NSCLC)中生长因子受体(EGFR)基因突变与临床特点相关性。方法采用探针扩增阻滞突变系统(ARMS)检测102例手术后组织标本的EGFR基因突变情况。结果 102例NSCLC组织中EGFR突变率为50.98%,外显子19、21突变率为67.31%。男性和女性的突变率分别为33.33%和64.91%,吸烟与不吸烟患者的EGFR基因突变率分别为37.50%、59.68%,中高度分化和低分化患者的EGFR基因突变率分别为59.02%、39.02%,腺癌和鳞癌中的突变率分别为59.04%、6.25%,差异均有统计学意义(均P<0.05)。>60岁患者与≤60岁患者的EGFR基因突变率分别为44.93%、63.64%,术后临床分期Ⅰ+Ⅱ和Ⅲ期的EGFR基因突变率分别为49.32%、55.17%,淋巴转移和无淋巴结转移者的突变率分别为43.90%、55.74%(均P>0.05)。结论 EGFR基因突变与性别、吸烟、腺癌、分化程度有关。 Objective To investigate the correlation of epidermal growth factor receptor (EGFR) gene mutations and clinicopathological characteristics in patients with non-small cell lung cancer (NSCLC). Methods One hundred and two surgical specimens were collected from patients with NSCLC. The EGFR gene mutations were detected by scorpion amplification refractory mutation system (ARMS). Results The mutation rate of EGFR was 50.98% and that of exon 19/21 was 67.31%. The mutation rates of male and female were 33.33/ and 64.91/, smokers and non-smokers were 37.50/ and 59.68/, medium to high differentiated NSCLC and poorly differentiated NSCLC were 59.02% and 39.02%, adenocarcinoma and squamous cell carcinoma were 59.04% and 6.25%(all P〈0.05). The mutation rates of patients aged 〉60 years and ^60 years were 44.93% and 63.64%, clinical stages I + I and clinical stages III were 49.32% and 55.17%, lymphatic metastasis and no lymphatic metastasis were 43.90% and 55.74% (all P 〉0.05). Conclusion The EGFR gene mutations are correlated with sex, smoking status, pathological type and differentiation of NSCLC patients.
作者 张军 张凡 周礼湘 徐立栋 高军 ZHANG Jun ZHANG Fan ZHOU Lixiang et at(Department of Thoracic Surgery, Jiaxing Second Hospital, Jiaxing 314000, China)
出处 《浙江医学》 CAS 2017年第20期1745-1747,共3页 Zhejiang Medical Journal
基金 嘉兴市科技局立项课题(2013AY21060)
关键词 非小细胞肺癌 表皮生长因子受体 基因突变 Non-small celllung cancers Epidermal growth factor Receptorgenesmutation
  • 相关文献

参考文献8

二级参考文献70

  • 1BaoMingQIN,XiaoCHEN,JingDeZHU,DuanQingPEI.Identification of EGFR kinase domain mutations among lung cancer patients in China:implication for targeted cancer therapy[J].Cell Research,2005,15(3):212-217. 被引量:69
  • 2杨玲,李连弟,陈育德,D.M.Parkin.中国2000年及2005年恶性肿瘤发病死亡的估计与预测[J].中国卫生统计,2005,22(4):218-221. 被引量:337
  • 3杨玲,李连弟,陈育德,Donald Maxwell Parkin.中国肺癌死亡趋势分析及发病、死亡的估计与预测[J].中国肺癌杂志,2005,8(4):274-278. 被引量:167
  • 4董强刚,韩宝惠,黄进肃,杨立民,黄建,赵春英,卢丽琴.176例非小细胞肺癌的EGFR基因突变分析[J].中华肿瘤杂志,2006,28(9):686-690. 被引量:53
  • 5Maria Sibilia, Renate Kroismayr, Beate M, et al. The epidermal growth factor receptor: from development to Tumorigenesis. Differentiation, 2007, 75(9): 770-787.
  • 6Lynch TJ, Bell DW, SordeUa R, et al. Activating mutations in the epidermal growth factor receptor underlying responsiveness ofnon-small-cen lung cancer to gefitinib. N EnglJ Med, 2004, 350(21): 2129-2139.
  • 7Paez JG, Janne PA, Lee JC, et al. EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy. Science, 2004, 304(5676): 1497-1500.
  • 8Kosaka T, Yatabe Y, Endoh H, et al. Mutations of the epidermal growth factor receptor gene in lung cancer: biological and clinical implecations. Cancer Res, 2004, 64(24): 8919-8923.
  • 9Cappuzzo F, Hirsch FR, Rossi E, et al. Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small cell lung cancer.J Natl Cancer Inst, 2005, 97(9): 643-655.
  • 10Han SW, Kim TY, Jeon YK, et al. Optimization of patient selection for gefitinib in non-small cell lung cancer by combined analysis of epidermal growth factor receptor mutation, K-ras mutation, and Akt phosphorylation. Clio Cancer Res, 2006, 12(8): 2538-2544.

共引文献182

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