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Expression Patterns of Coagulation Factor XIII Subunit A on Leukemic Lymphoblasts Correlate with Clinical Outcome and Genetic Subtypes in Childhood B-cell Progenitor Acute Lymphoblastic Leukemia

机译:凝血因子XIII亚基A对白血病淋巴细胞的表达模式与儿童B细胞祖急性淋巴细胞白血病中的临床疗效和遗传亚型相关

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摘要

Background: Based on previous retrospective results, we investigated the association of coagulation FXIII subunit A (FXIII-A) expression pattern on survival and correlations with known prognostic factors of B-cell progenitor (BCP) childhood acute lymphoblastic leukemia (ALL) as a pilot study of the prospective multi-center BFM ALL-IC 2009 clinical trial. Methods: The study included four national centers ( = 408). Immunophenotyping by flow cytometry and cytogenetic analysis were performed by standard methods. Copy number alteration was studied in a subset of patients ( = 59). Survival rates were estimated by Kaplan-Meier analysis. Correlations between FXIII-A expression patterns and risk factors were investigated with Cox and logistic regression models. Results: Three different patterns of FXIII-A expression were observed: negative (<20%), dim (20–79%), and bright (≥80%). The FXIII-A dim expression group had significantly higher 5-year event-free survival (EFS) (93%) than the FXIII-A negative (70%) and FXIII-A bright (61%) groups. Distribution of intermediate genetic risk categories and the “B-other” genetic subgroup differed significantly between the FXIII-A positive and negative groups. Multivariate logistic regression confirmed independent association between the FXIII-A negative expression characteristics and the prevalence of intermediate genetic risk group. Conclusions: FXIII-A negativity is associated with dismal survival in children with BCP-ALL and is an indicator for the presence of unfavorable genetic alterations.
机译:背景:基于先前的回顾结果,我们研究了凝血FXIII亚基A(FXIII-A)表达模式对生存和相关性与已知的B细胞祖(BCP)儿童急性淋巴细胞白血病(全部)作为飞行员的生存和相关性预期多中心BFM All-IC 2009临床试验研究。方法:该研究包括四个国家中心(= 408)。通过流式细胞术和细胞遗传学分析的免疫蛋白酶通过标准方法进行。在患者的子集中研究了拷贝数改变(= 59)。 Kaplan-Meier分析估计生存率。 COX和Logistic回归模型研究了FXIII-A表达模式和风险因素之间的相关性。结果:观察到三种不同的FXIII模式 - A表达:阴性(<20%),暗淡(20-79%),亮(≥80%)。 FXIII-A昏暗的表达组比FXIII-A负(70%)和FXIII-A亮(61%)组具有显着更高的5年的无需存活(EF)(93%)。中间遗传风险类别的分布和“B-oder”遗传亚组在FXIII-A阳性和阴性群之间有显着差异。多变量逻辑回归证实了FXIII-A阴性表达特征与中等遗传风险组的患病率之间的独立关联。结论:FXIII-A消极性与BCP的儿童的惨淡生存有关,并且是存在不利遗传改变的指标。

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