期刊文献+
共找到2篇文章
< 1 >
每页显示 20 50 100
GPC-1、miRNA-9及Caspase-3在肺腺癌中的表达及与病情和预后生存的相关性 被引量:4
1
作者 智雅婧 冯铁虹 +1 位作者 那顺孟和 郑媞 《分子诊断与治疗杂志》 2020年第12期1686-1690,共5页
目的探讨磷脂酰肌醇蛋白多糖-1(GPC-1)、微小RNA-9(miRNA-9)及天冬氨酸特异性半胱氨酸蛋白酶-3(Caspase-3)在肺腺癌中的表达及与病情、预后生存的相关性。方法 2015年8月至2017年8月本院收治的肺腺癌患者的临床资料进行整理、分析(76份... 目的探讨磷脂酰肌醇蛋白多糖-1(GPC-1)、微小RNA-9(miRNA-9)及天冬氨酸特异性半胱氨酸蛋白酶-3(Caspase-3)在肺腺癌中的表达及与病情、预后生存的相关性。方法 2015年8月至2017年8月本院收治的肺腺癌患者的临床资料进行整理、分析(76份肺腺癌组织标本及76份癌旁正常组织标本),采用免疫组化染色法对比肺腺癌组织及癌旁正常组织中GPC-1、miRNA-9及Caspase-3表达情况。结果肺腺癌组织中GPC-1阳性表达率、Caspase-3阴性表达率、miRNA-9高表达率明显高于癌旁正常组织(P<0.05)。GPC-1、miRNA-9及Caspase-3表达情况与肺腺癌患者年龄、性别、分化程度、肿瘤直径、血管侵犯无关(P>0.05);与TNM分期、淋巴结转移有关(P<0.05)。76例肺腺癌患者3年生存率为35.53%(49/76),GPC-1阳性表达、miRNA高表达、Caspase-3阴性表达的肺腺癌患者死亡率更高(P<0.05)。生存分析显示GPC-1(表达阴性)、miRNA-9(低表达)、Caspase-3(阳性表达)者生存期较长,Keplan-meier生存曲线明显不同(P<0.05)。临床分期(Ⅲ~Ⅵ期)、有淋巴结转移、GPC-1表达(阳性)、miRNA(高表达)及Caspase-3表达(阴性)为影响肺腺癌患者预后生存的独立危险因素(P<0.05)。结论GPC-1、miRNA、Caspase-3异常表达与肺腺癌患者病情进展密切相关,且不利于患者预后。 展开更多
关键词 GPC-1 miRNA-9 CASPASE-3 肺腺癌中 病情 预后生存
下载PDF
Treatment and survival status of patients with EGFR mutation-positive stage Ⅳ lung adenocarcinoma: five-year follow-up results in the Ordos Area of Inner Mongolia, China
2
作者 Gaowa Jin Wenjuan Wang +14 位作者 Shuqin Deng Caihong Jiang Xiaojun Bai Jun Zhao Feng Chen Jixiang Hou Lanzhen Zhao Hui Li Ziyu Lu Lenggaowa Da Yungaowa Wu Xiaoyun Ma Yahan Wu Jiali Gao Quanfu Li 《Oncology and Translational Medicine》 2018年第4期158-162,共5页
Objective We aimed to determine the epidermal growth factor receptor (EGFR) mutation status and treatment survival of patients with stage IV lung adenocarcinoma living in the Ordos area of Inner Mongolia, China. Met... Objective We aimed to determine the epidermal growth factor receptor (EGFR) mutation status and treatment survival of patients with stage IV lung adenocarcinoma living in the Ordos area of Inner Mongolia, China. Methods EGFR testing and first-line tyrosine kinase inhibitor (TKI) treatment rates of patients with stage IV lung adenocarcinoma were analyzed from June 2012 to June 2016. Kaplan-Meier survival curves were constructed to compare patients who received different treatment strategies and those harboring different EGFR mutation statuses. Results EGFR testing and mutation rates were 65.60% and 52.90%, respectively, and improved continuously from June 2012 to June 2016. Among patients with EGFR mutations, 38.9% had EGFR 19 del, 48.2% had L858R, 4.2% had co-existing mutations in exons 19 and 21, and 8.4% had uncommon mutations. The median overall survival (OS) was 29.5, 26.5, and 16.0 months for patients receiving both TKI and chemotherapy, TKI alone, and chemotherapy alone, respectively (P = 0.047). The OS was 26.5 and 30.0 months for patients harboring EGFR 19 del and L858R mutations, respectively (P = 0.096). Conclusion The high OS rates of stage IV lung adenocarcinoma patients living in the Ordos area may be attributed to continuous improvements in EGFR testing and first-line TKI treatment rates. In the era of TKIs, chemotherapy for increasing OS times should be emphasized. 展开更多
关键词 epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) minority areas
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部