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European LeukemiaNet study on the reproducibility of bone marrow features in masked polycythemia vera and differentiation from essential thrombocythemia

机译:欧洲白血病肿瘤骨髓特征再现性与基本血小伤症的骨髓特征再现性研究

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The purpose of the study was to assess consensus and interobserver agreement among an international panel of six hematopathologists regarding characterization and reproducibility of bone marrow (BM) histologic features used to diagnose early stage myeloproliferative neoplasms, in particular differentiation of so-called masked/prodromal polycythemia vera (mPV) from JAK2-mutated essential thrombocythemia (ET). The six members of the hematopathology panel evaluated 98 BM specimens independently and in a blinded fashion without knowledge of clinical data. The specimens included 48 cases of mPV according to the originally published hemoglobin threshold values for this entity (male: 16.0-18.4 g/dL, female: 15.0-16.4 g/dL), 31 cases with overt PV according to the updated 2016 WHO criteria, and 19 control cases. The latter group included cases of JAK2-mutated ET, primary myelofibrosis, myelodysplastic syndrome, and various reactive conditions. Inter-rater agreement between the panelists was very high (overall agreement 92.6%, kappa 0.812), particularly with respect to separating mPV from ET. Virtually all cases of mPV were correctly classified as PV according to their BM morphology. In conclusion, a central blinded review of histology slides by six hematopathologists demonstrated that highly reproducible specific histological pattern characterize PV and confirmed the notion that there are no significant differences between mPV and overt PV in relation to BM morphology.
机译:该研究的目的是评估六种血液病理学家国际小组之间的共识和Interobserver协议,关于骨髓(BM)组织学特征的表征和再现性,用于诊断早期肌酚肌肉瘤的特征,特别是所谓的掩蔽/前驱性多胆症的分化来自JAK2-突变的基本血小板血症(ET)的VERA(MPV)。造血病理学面板的六个成员独立评估了98个BM标本,并以盲目的方式进行了盲目的方式,而不知道临床数据。根据本实体最初出版的血红蛋白阈值(男性:16.0-18.4g / dl,女性:15.0-16.4g / dl),根据最新的2016年,根据2016年的最新标准,根据最初发表的血红蛋白阈值,包括48例MPV和19个控制案例。后者群包括JAK2-突变的ET,原发性髓颤,骨髓增生术综合征和各种反应性条件的病例。小组成员之间的帧间间协议非常高(总协议92.6%,Kappa 0.812),特别是与分离IE的MPV。几乎所有MPV的病例都根据其BM形态正确归类为PV。总之,通过六个造血学家对组织学载玻片的核心盲化审查证明了高度可重复的特定组织学模式表征PV并确认了在与BM形态相关的MPV和公开PV之间没有显着差异的观点。

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