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海岛地区非小细胞肺癌EGFR基因突变与临床病理特征的关系 被引量:1

Relationship of epidermal growth factor receptor gene mutations in exons 19 and 21 and clinicopathologic features in patients with non-small cell lung cancer (NSCLC) in ZhouShan Archipelago
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摘要 目的:探讨舟山海岛地区非小细胞肺癌患者表皮生长因子受体(EGFR)19、21外显子的基因突变发生率及其与临床病理特征的相关性。方法:应用PCR扩增产物直接测序法检测129例非小细胞肺癌患者肿瘤组织EGFR基因19、21外显子突变,并分析其与临床病理资料的相关性。结果:129例肺癌患者中,共有35例发生EGFR基因突变(27.1%)。女性、非吸烟、腺癌及中高分化NSCLC患者EGFR基因突变率较高,是引起EGFR基因突变的危险因素(P<0.05)。Kaplan-Meier生存分析显示,NSCLC患者EGFR基因野生型及突变型生存率比较差异无统计学意义(P>0.05)。结论:舟山海岛地区肺癌患者EGFR突变发生率为27.1%,在女性、非吸烟、中高分化及肺腺癌患者中多见,但与总生存时间无明显相关。 Objective: To investigate epidermal growth factor receptor (EGFR) gene mutations in exons 19 and 21 of patients with non - small cell lung cancer (NSCLC) and to analyze the relationship of EGFR mutations with clinicopathologic features in Zhoushan Archipelago. Methods: The EGFR gene exons 19 and 21 of tumor tissue were amplified by PCR, followed by direct sequencing in 129 surgically - removed specimens of NSCLC. The relationship of EGFR gene mutations in NSCLC with clinicopathologic features and prognosis were analyzed. Results: EGFR mutations were detected in 35 cases of 129 (27.1%) patients with NSCLC. Mutations were more frequently observed in women, non - smokers, adenocarcinoma patients and well - differentiated NSCLC patients, which were the risk factors for EGFR mutation (P 〈 0.05 ). Kaplan - Meier survival analysis showed that the overall survival time of NSCLC patients with wild- type EGFR had no significant difference with patients with mutated EGFR(P 〉 0.05 ). Conclusion: The rate of EGFR mutations occurred in Zhoushan Archipelago was 27. 1%, more frequently in females, non -smokers, adenocarcinoma patients and well -differentiated NSCLC patients, but it had no significant correlation with overall survival time.
出处 《中国卫生检验杂志》 CAS 北大核心 2013年第6期1359-1363,共5页 Chinese Journal of Health Laboratory Technology
基金 浙江省科技厅项目(2011C37030)
关键词 非小细胞肺癌 表皮生长因子受体 基因突变 表皮生长因子受体酪氨酸激酶抑制剂 Non - small cell lung cancer Epidermal growth factor receptor Gene mutation EGFR - tyrosine kinase inhibitor
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