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作 者:刘艳艳[1] 姚书娜[1] 姚志华[1] 郭宏强[1] 赵燕[1] 贾彦召[1] 杨树军[1]
机构地区:[1]河南省肿瘤医院郑州大学附属肿瘤医院内科,郑州450008
出 处:《白血病.淋巴瘤》2011年第8期468-470,共3页Journal of Leukemia & Lymphoma
摘 要:目的探讨p53突变蛋白表达对弥漫大B细胞淋巴瘤(DLBCL)预后的预测作用,指导个体化治疗。方法随机选择初治DLBCL患者62例,应用免疫组织化学方法检测p53突变蛋白和CD。bel-6、MUM1的表达,分析p53突变蛋白表达与患者临床特征、分子分型以及预后的关系。结果48.4%(30/62)的患者表达p53突变蛋白。p53突变蛋白表达与初始治疗反应有关(X^2=20.365,P=0.040),阳性组的完全缓解率为33.3%(10/30),阴性组为59.4%(19/21);与分子分型有关(X^2=31.023,P=0.021),阳性组非生发中心型比例显著高于阴性组,分别为83.3%和56.2%;与其他临床特征无关。多因素生存分析显示p53突变蛋白表达是独立的预后预测因子,阳性组的无进展生存期和中位生存期均短于阴性组(X^2=36.784,P=0.005和X^2=35.276,P=0.006)。结论p53突变蛋白表达是DLBCL独立的不良预后因子,能够用来指导个体化治疗。Objective To explore the prognostic significance of p53 mutation protein in patients with diffuse large B-cell lymphoma for the purpose of individualized therapy. Methods Newly diagnosed 62 cases were randomly chosen from our hospital, p53 mutation protein and CD10, bel-6, MUM1 were tested by immunohistoehemistry. Correlation of p53 mutation protein with patients" characteristics, genotype and survival were analysed in the study. Results p53 mutation protein was found in 48.4 % (30/62) of patients. Its expression was only related to initial treatment response (X^2=20.365, P =0.040), including complete remission rate of 33.3 % (10/30) in positive group and 59.4 % (19/32) in negative group, and non-germinal center genotype (X^2=31.023, P =0.021) with 83.3 % in positive group and 56.2 % in negative group. No other correlation was not verified with clinical features. Multivariate survival analysis showed that p53 mutation protein was an independent predictor for shorter progress-free and overall survival in positive group (X^2= 30.784, P =0.005 and X^2 =35.276, P =0.006). Conclusion p53 mutation protein should be an independent predictor with poor prognosis and to direct personalized therapy.
关 键 词:淋巴瘤 大细胞 弥漫型 肿瘤抑制蛋白质P53 预后
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