摘要
目的:探讨细胞核转录因子(NF-κB)在胃癌及其淋巴结组织中表达的意义及CAPOX方案(卡培他滨+奥沙利铂)联合艾迪治疗胃癌的疗效,为临床治疗提供参考。方法:回顾性分析我院2008年1月~2009年6月收治的80例胃癌患者的临床资料,80例患者随机分为两组,实验组40例,行CAPOX方案(卡培他滨+奥沙利铂)联合艾迪治疗;对照组40例,单行CAPOX方案治疗。随访1~2年,治疗前取胃癌组织、转移淋巴结及正常胃组织,采用免疫组化法检测不同临床病理特征胃癌患者NF-κB的表达,并比较两组患者治疗前、后NF-κB的表达。结果:胃癌组织NF-κB表达与有无淋巴结转移、分化程度、Lauren分型有关(P<0.05),而与肿瘤大小无关(P>0.05)。随访期间组内比较,治疗后实验组、对照组患者NF-κB阳性表达率均低于治疗前,差异有统计学意义(P<0.05);两组间相比,治疗后实验组患者NF-κB阳性表达率低于对照组,差异有统计学意义(P<0.05)。结论:应用CAPOX方案联合艾迪化疗早期治疗胃癌及其淋巴结转移灶,可以显著降低患者NF-κB阳性表达率,有效提高患者的生存质量,可临床推广使用。
Objective: To investigate the expression of nuclear transcription factor(NF-κB) in gastric cancer and lymph node tissues and effectiveness of CAPOX program(capecitabine + oxaliplatin).Methods: Clinical data of 80 cases of gastric cancer admitted from January 2008 to June 2009 were analyzed retrospectively.They were randomly divided into two groups by half,experimental group with CAPOX program(capecitabine + oxaliplatin) and Eddie treatment,and control group with single CAPOX program.They were followed up for 1-2 years.Before the treatment,gastric cancer tissue,lymph nodes and normal gastric tissue were taken for detection of NF-κB expression by immunohistochemical method,and the expression was compared before and after treatment.Results: NF-κB expression was associated with lymph node metastasis,differentiation,and Lauren type(P〈0.05),but had nothing to do with the tumor size(P〈0.05).Follow-up showed after treatment expression of NF-κB was significantly lower than that before treatment in two groups(P〈0.05).After treatment,expression of NF-κB was significantly lower in experimental group(P〈0.05).Conclusion: Early treatment with CAPOX program and Eddie chemotherapy can significantly decrease expression of NF-κB and effectively improve patients′ life quality.It is worthy clinical application.
出处
《海南医学院学报》
CAS
2011年第12期1621-1623,共3页
Journal of Hainan Medical University
基金
海南医学院科研基金资助学报项目(0020110445)
Hainan Medical University Scientific Research Fund Supported Project of the Journal(0020110445)
关键词
胃癌
淋巴结转移灶
细胞核转录因子
化疗
Gastric cancer
Lymph node metastases
Nuclear transcription factor
Chemotherapy