首页> 美国卫生研究院文献>Springer Open Choice >Cytomorphology review of 100 newly diagnosed lower-risk MDS patients in the European LeukemiaNet MDS (EUMDS) registry reveals a high inter-observer concordance
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Cytomorphology review of 100 newly diagnosed lower-risk MDS patients in the European LeukemiaNet MDS (EUMDS) registry reveals a high inter-observer concordance

机译:在欧洲白血病网MDS(EUMDS)注册表中对100名新诊断的低危MDS患者的细胞形态学检查显示观察者之间存在高度一致性

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摘要

The European LeukemiaNet MDS (EUMDS) registry is collecting data of myelodysplastic syndrome (MDS) patients belonging to the IPSS low or intermediate-1 category, newly diagnosed by local cytologists. The diagnosis of MDS can be challenging, and some data report inter-observer variability with regard to the assessment of the MDS subtype. In order to ensure that correct diagnoses were made by the participating centres, blood and bone marrow slides of 10% of the first 1000 patients were reviewed by an 11-person panel of cytomorphologists. All slides were rated by at least 3 panel members (median 8 panel members; range 3–9). Marrow slides from 98 out of 105 patients were of good quality and therefore could be rated properly according to the WHO 2001 classification, including assessment of dysplastic lineages. The agreement between the reviewers whether the diagnosis was MDS or non-MDS was strong with an intra-class correlation coefficient (ICC) of 0.85. Six cases were detected not to fit the entry criteria of the registry, because they were diagnosed uniformly as CMML or AML by the panel members. The agreement by WHO 2001 classification was strong as well (ICC = 0.83). The concordance of the assessment of dysplastic lineages was substantial for megakaryopoiesis and myelopoiesis and moderate for erythropoiesis. Our data show that in general, the inter-observer agreement was high and a very low percentage of misdiagnosed cases had been entered into the EUMDS registry. Further studies including histomorphology are warranted.
机译:欧洲LeukemiaNet MDS(EUMDS)注册中心正在收集属于局部细胞学家新诊断的IPSS低或中1类的骨髓增生异常综合症(MDS)患者的数据。 MDS的诊断可能具有挑战性,并且一些数据报告了关于MDS亚型评估的观察者间差异。为了确保参与中心做出正确的诊断,由11人组成的细胞形态学家小组对前1000名患者中10%的血液和骨髓切片进行了检查。所有幻灯片均至少由3名小组成员进行评分(中位数为8名小组成员;范围为3–9)。 105名患者中有98名骨髓载玻片质量良好,因此可以根据WHO 2001分类标准,包括对发育不良谱系的评估,对它们进行适当的评级。审稿人之间的诊断是MDS还是非MDS的一致性很强,组内相关系数(ICC)为0.85。检测到六例不符合注册表的输入标准,因为专家组成员将它们统一诊断为CMML或AML。世卫组织2001年分类的协议也很强(ICC = 0.83)。异常增生谱系的评估一致性对于巨核细胞生成和骨髓生成是实质性的,而对于红细胞生成则是中等的。我们的数据表明,总体而言,观察员之间的同意很高,并且误诊病例的输入率非常低,已经输入到EUMDS注册表中。包括组织形态学在内的进一步研究是必要的。

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