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作 者:张瑞东[1] 李志刚[1] 刘怡[1] 张永红[1] 谢静[1] 石慧文[1] 郑胡镛[1] 吴敏媛[1]
机构地区:[1]首都医科大学附属北京儿童医院,北京100045
出 处:《中国小儿血液与肿瘤杂志》2009年第4期154-157,共4页Journal of China Pediatric Blood and Cancer
摘 要:目的分析髓系抗原阳性(My+)的儿童高危急性淋巴细胞白血病(ALL)的临床生物学特征及长期预后关系。方法采用流式细胞仪直接免疫荧光法及RT-PCR法分别检测2001年8月至2003年3月在我院收治的初诊高危112例ALL患儿的髓系抗原及融合基因的表达,对其预后进行了中位时间达76个月的长期观察。结果髓系抗原的表达率为30.4%,B系ALL表达髓系抗原多于T系ALL,差异有显著性意义(P=0.019)。My+ALL患儿携带TEL-AML1融合基因者多于My-ALL患儿(P=0.049),My+ALL与My-ALL患儿在临床特点以及疗效等方面两组之间差异无显著性意义。结论高危ALL无论有无髓系抗原的表达其疗效无显著性差异,髓系抗原阳性表达在高危儿童ALL时不能作为预后不良的因素。Objective To observe myeloid antigen expression and its relationship with clinical and biological features as well as long-term prognosis in children with high-risk (HR) acute lymphoblastic leukemia (ALL). Methods The expression of myeloid antigen and fusion gene of 112 children with HR-ALL from August of 2001 to March of 2003 were measured respectively by 3-color flow cytometry and RT-PCR, the impact of myeloid antigen expression on clinical prognosis were studied for a median time of 76 months. Results The total positive cases of myeloid antigen expression were 34 (30.4%). Myeloid antigen expression in B-ALL group were significant higher than that in T-ALL group (P = 0. 019) ; TEL/ AML1 positive in My^+ ALL group were more than in My^- ALL group (P =0. 049). There were no significant differences between My^+ ALL group and My^-ALL group in clinical features and treatment outcome. Conclusion Myeloid antigen expression is not an independent prognostic factor in HR-ALL patients.
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