Common genetic abnormalities and phenotypic scoring in Saudi patients with acute B-lymphoblastic leukemia

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Maha A Alanazi, F. Alzahrani, S. Shaikh, Amir H Msmar, F. Hassan
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引用次数: 0

Abstract

Introduction: B-acute lymphoblastic leukemia (B-ALL) is a malignant neoplasm of hematopoietic stem cells originating in bone marrow and characterized by proliferation of blast cells of lymphoid series. The aim of this study was to predictive scoring system (SS) using a fully standardized EuroFlow eight-color panel. Methods: The expression of the different cluster of differentiation (CD) markers involved in the B-ALL EuroFlow panel was investigated by measuring their positivity, percentage, and median fluorescence intensity. Results: CD9, CD123, and TdT were used to predict TCF3PBX1 with 80.0% sensitivity (SN) and 100% specificity (SP). CD20 and CD66 were used to predict hypoploidy with 63.0% SN and 100% SP. As a result, no useful discriminative SS was developed. Conclusions: Four SSs were proposed for the prediction of the most common cytogenetic abnormalities of Saudi B-ALL.
沙特急性B淋巴细胞白血病患者常见遗传异常和表型评分
简介:B型急性淋巴细胞白血病(B-ALL)是一种起源于骨髓的造血干细胞恶性肿瘤,其特征是淋巴系母细胞增殖。本研究的目的是使用完全标准化的EuroFlow八色面板建立预测评分系统(SS)。方法:通过测量B-ALL EuroFlow面板中不同分化簇(CD)标记的阳性率、百分比和中位荧光强度来研究其表达。结果:CD9、CD123和TdT用于预测TCF3PBX1,敏感性(SN)为80.0%,特异性(SP)为100%。CD20和CD66用于预测具有63.0%SN和100%SP的低倍性。因此,没有开发出有用的判别性SS。结论:提出了四种SS来预测沙特B-ALL最常见的细胞遗传学异常。
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来源期刊
Electronic Journal of General Medicine
Electronic Journal of General Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.60
自引率
4.80%
发文量
79
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