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European Bone Marrow Working Group trial on reproducibility of World Health Organization criteria to discriminate essential thrombocythemia from prefibrotic primary myelofibrosis

机译:欧洲骨髓工作组关于世界卫生组织标准的可重复性试验,用于将原发性血小板增多症与原发性原发性骨髓纤维化区别开来

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Background The World Health Organization classification of myeloproliferative neoplasms discriminates between essential thrombocythemia and the prefibrotic phase of primary myelofibrosis. This discrimination is clinically relevant because essential thrombocythemia is associated with a favorable prognosis whereas patients with primary myelofibrosis have a higher risk of progression to myelofibrosis or blast crisis. Design and Methods To assess the reproducibility of the classification, six hematopathologists from five European countries re-classified 102 non-fibrotic bone marrow trephines, obtained because of sustained thrombocytosis. Results Consensus on histological classification defined as at least four identical diagnoses occurred for 63% of the samples. Inter-observer agreement showed low to moderate kappa values (0.28 to 0.57, average 0.41). The percentage of unclassifiable myeloproliferative neoplasms rose from 2% to 23% when minor criteria for primary myelofibrosis were taken into account. In contrast, the frequency of primary myelofibrosis dropped from 23% to 7%, indicating that the majority of patients with a histological diagnosis of primary myelofibrosis did not fulfill the complete criteria for this disease. Thus, over 50% of cases in this series either could not be reproducibly classified or fell into the category of unclassifiable myeloproliferative neoplasms. Conclusions World Health Organization criteria for discrimination of essential thrombocythemia from prefibrotic primary myelofibrosis are poorly to only moderately reproducible and lead to a higher proportion of non-classifiable myeloproliferative neoplasms than histology alone.
机译:背景世界卫生组织对骨髓增生性肿瘤的分类将原发性血小板增多症与原发性骨髓纤维化的纤维化前期区分开来。这种区别在临床上是相关的,因为原发性血小板增多症与预后良好相关,而原发性骨髓纤维化的患者发展为骨髓纤维化或母细胞危象的风险更高。设计和方法为了评估分类的可重复性,来自五个欧洲国家的六位血液病理学家对由于持续的血小板增多症而获得的102例非纤维化的骨髓白喉细胞进行了重新分类。结果组织学分类的共识定义为63%的样本至少进行了四次相同的诊断。观察员之间的共识表明,卡伯值低至中(0.28至0.57,平均值为0.41)。当考虑到原发性骨髓纤维化的次要标准时,无法分类的骨髓增生性肿瘤的比例从2%上升到23%。相反,原发性骨髓纤维化的发生率从23%下降到7%,这表明大多数经组织学诊断为原发性骨髓纤维化的患者并未达到该疾病的完整标准。因此,该系列中超过50%的病例无法重现分类或属于无法分类的骨髓增生性肿瘤。结论世界卫生组织用于区分原发性纤维化前原发性骨髓纤维化的原发性血小板增多症的标准差,只能中等程度地重现,导致无法分类的骨髓增生性肿瘤所占比例要高于单独的组织学。

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