新辅助化疗对乳腺癌组织中ER、Survivin及C-erB-2表达的影响  被引量:8

Neoadjuvant chemotherapy for breast cancer ER,survivin and the C-erB-2 expression

在线阅读下载全文

作  者:李朝战[1] 黄勇[1] 杨慧[1] 王星际[1] 张超[1] 

机构地区:[1]山东省枣庄市立医院普外科,山东枣庄277000

出  处:《中国现代普通外科进展》2010年第9期688-690,722,共4页Chinese Journal of Current Advances in General Surgery

摘  要:目的:探讨乳腺癌新辅助化疗的临床效果及其对ER、Survivin和C-erB-2表达的影响。方法:62例可手术乳腺癌采用TE方案新辅助化疗观察客观有效率及新辅助化疗前后ER、Survivin和C-erB-2的表达。结果:新辅助化疗后临床完全缓解(CR)9例,部分缓解(PR)38例,病情稳定(SD)14例,疾病进展(PD)1例。新辅助化疗后Survivin表达明显下降(P<0.05),ER及C-erB-2阳性表达率均低于新辅助化疗前但差异无统计学意义(P>0.05)。Survivin化疗后表达降低者化疗有效率高,Survivin表达升高者化疗有效率低,二者之间有相关性,ER、C-erB-2表达变化与化疗有效率之间无相关性。结论:乳腺癌新辅助化疗可以有效的缩小肿瘤;Survivin在新辅助化疗后表达显著降低,而ER、及C-erB-2的阳性表达降低,但无显著影响。Objective:To investigate the clinical effect of neoadjuvant chemotherapy to breast cancerand the influence to the ER,Survivin and C-erB-2 expression.Methods:sixtytwo patients of operable breast cancer were treated with neoadjuvant chemotherapy TE program.The ER,Survivin and C-erB-2 expression were observated before and after neoadjuvant chemotherapy.Results:Afterneoadjuvant chemotherapy clinical complete remission(CR)in 9 cases,partial remission(PR)in 38 cases,stable disease (SD)in 14 cases,no disease progression (PD)in 1 case.Afterneoadjuvant chemotherapy Survivin expression was significantly decreased (P〈0.05),ER and C-erB-2 positive expression rate were lower with no significant difference (P〉0.05).The efficiency of chemotherapy were low in patients with increased Survivin expression and the efficiency were high in patients with decrsased Survivin expression.There was no significant relation between the ER,C-erB-2 expression and the efficiency of chemotherapy.Conclusion:Neoadjuvant chemotherapy in breast cancer can effectively reduce the tumor;Survivin expression after neoadjuvant chemotherapy depresses significantly and the positive expression of ER and C-erB-2 positive depress with no signficant effect.

关 键 词:乳腺肿瘤 新辅助化疗 ER SURVIVIN C-ERB-2 

分 类 号:R737.9[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象