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A new score including CD43 and CD180: Increased diagnostic value for atypical chronic lymphocytic leukemia

机译:包括CD43和CD180的新分数:非典型慢性淋巴细胞白血病的诊断价值增加

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摘要

Moreau score has been used to differentiate chronic lymphocytic leukemia (CLL) from other mature B‐cell neoplasms. However, it showed limitations in Asian patients. Therefore, we conducted a new score system replacing CD5 and CD23 with CD43 and CD180 to evaluate its diagnostic value of CLL. 237 untreated samples diagnosed with mature B‐cell neoplasms were collected and were randomly divided into an exploratory and a validation cohort by a 2:1 ratio. The expression of CD5, CD19, CD20, CD23, CD43, CD79b, CD180, CD200, FMC7, and surface immunoglobulin (SmIg) were analyzed among all the samples. A proposed score was developed based on the logistic regression model. The sensitivity and specificity of the proposed score were calculated by ROC curves. CD43/CD180, CD200, FMC7, and CD79b were included in our new CLL score, which showed a sensitivity of 91.8% and a specificity of 83.1%. These results were confirmed in a validation cohort with a sensitivity of 90.5% (p = 0.808) and a specificity of 79.5% (p = 0.639). In CD5 negative or CD23 negative CLL group, the new CLL score displayed improved sensitivity of 79.4% compared to Moreau score and CLLflow score (41.2% and 47.1%, respectively). In atypical CLL group, the new CLL score showed improved sensitivity of 84.2% compared to Moreau score and CLLflow score (61.4% and 64.9%, respectively). This proposed atypical CLL score helped to offer an accurate differentiation of CLL from non‐CLL together with morphological and molecular methods, particularly in Chinese patients with atypical immunophenotype.
机译:莫罗得分已被用于区分其它成熟B细胞肿瘤慢性淋巴细胞性白血病(CLL)。然而,这表明在亚洲患者的局限性。因此,我们进行了新的评分系统,CD43和CD180更换CD5和CD23评估CLL的诊断价值。 237个诊断为成熟B细胞肿瘤未处理的样品收集和由2随机分为探索和验证队列:1的比例。所有样品中CD5,CD19,CD20,CD23,CD43,CD79b的,CD180,CD200,FMC7,和表面免疫球蛋白(SMIG)的表达进行了分析。拟议的得分是基于逻辑回归模型开发。所提出的得分的敏感性和特异性通过ROC曲线计算。 CD43 / CD180,CD200,FMC7和CD79b的被列入我们的新CLL得分,这表明91.8%的敏感性和83.1%的特异性。这些结果与90.5%的灵敏度(P = 0.808)和79.5%(P = 0.639)具有特异性的验证队列得到了证实。在CD5阴性或CD23阴性CLL基,新CLL得分相比莫罗得分和CLLflow分数(分别为41.2%和47.1%,)显示的79.4%提高了灵敏度。在非典型CLL组,新的CLL得分相比莫罗得分和CLLflow分数(分别为61.4%和64.9%,)显示的84.2%提高了灵敏度。这项拟议非典型CLL得分帮助提供CLL的从形态学和分子生物学方法,尤其是在中国患者非典型免疫非CLL在一起准确的分化。

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