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作 者:谷仁凯[1] 卢洁[1] 孙立荣[1] 董增义[1] 雷炜[1] 庞秀英[1] 佟琳如[1] 周容[1]
机构地区:[1]青岛大学医学院附属医院儿内科
出 处:《中华儿科杂志》1999年第5期267-270,共4页Chinese Journal of Pediatrics
摘 要:目的探讨采用筑巢式聚合酶链反应(NestedPCR)等多项指标监测小儿急性淋巴细胞白血病(ALL)微量残留病(MRD)的临床意义。方法98例ALL进行了形态学、免疫学和细胞遗传学(MIC)分型,结合NestedPCR、姐妹染色单体交换(SCE)、染色体核型分析,对58例ALL进行MRD监测。结果:(1)58例ALL进行了T细胞受体(TCR)Vδ2Dδ3基因重排检测,在41例BALL中34例(83%)及4例TALL中1例具有此基因重排。检测敏感度为10-5~10-6。(2)58例ALL中44例ALL进行了MRDPCR动态监测。结果显示,维持强化治疗期间PCR检测由阴性转为阳性或持续阳性者,易引起骨髓复发死亡,提示预后较差。PCR检测转阴时间有明显的个体差异性,持续完全缓解(CCR)3年以上的ALL患儿PCR持续转阴可作为停用化疗药的可靠指标。(3)50例ALL进行了SCE的动态监测,初发组SCE频率高于CR组,差异有非常显著意义(P<0.001)。部分缓解组显著高于CR组(P<0.01),SCE频率变化与疾病的严重程度呈平行关系。(4)初发ALL中无论染色体核型正常或异常其SCE频率均显著增高,两者?Objective To explore the clinical significance of detecting minimal residual disease (MRD) in children with acute lymphoblastic leukemia (ALL) by using the methods of nestpolymerase chain reaction (NestPCR) and other detecting indexes. Methods Based on the morphological, immunological and cytogenetic (MIC) classifications along with the detection of NestPCR, the frequency of the sister chromatid exchange (SCE) and the chromosome karyotype analysis, 98 children with ALL were classified and 58 of 98 patients with ALL were detected for MRD. Results Fiftyeight patients with ALL were detected for gene rearrangements of T cell receptor (TCR) V2D3. Thirtyfour of 41 patients with BALL (82.9%) and 1 of 4 patients with TALL were found with the gene rearrangement. The detecting senstivities of MRD were 10-510-6. Fortyfour of 58 patients with ALL were detected dynamically for MRD. During intensive therapy, the patients with the positive PCR results converted from the negative and with the persistant positive PCR results preferred to relapse in bone marrow, which would induce death and indicate a poor prognosis. The time of PCR results turned to negative was different individually. It might be an indicator of terminating chemotherapy that the MRD was undetectable in ALL patients with continued complete remission (CCR) for more than 3 years. The frequencies of SCE of bone marrow cells in 50 patients with ALL were detected dynamically. The frequencies of SCE in patients with primary ALL and patients with partial remission were higher than patients with complete remission (CR) (P<0.001 and P<0.01, respectively). The frequency of SCE was associated with the severity of the disease. In patients with primary ALL, the frequencies of SCE were increased both in the groups of normal and abnormal chromosome karyotype
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