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A systematic classification of megakaryocytic dysplasia and its impact on prognosis for patients with myelodysplastic syndromes

机译:巨核细胞发育不良的系统分类及其对骨髓增生综合征患者的影响

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Dys-megakaryopoiesis is defined as?≥10?% of dysplastic megakaryocytes in bone marrow smears by the World Health Organization. However, concordance rates for dysplastic megakaryocytes between different observers is low and, consequently, evaluation of dysmegakaryopoiesis is also often discordant. We performed CD41 immune staining and proposed a systematic classification of dys-megakaryopoiesis on bone marrow films: (1) micro-megakaryocytes (12?μm); (2) micro-megakaryocytes (12-40?μm) with 1 nucleus; (3) micro-megakaryocytes (12-40?μm) with 2 nuclei; (4) micro-megakaryocytes (12-40 um) with multiple (more than 2) nuclei; (5) dysplastic megakaryocytes (≥40?μm) with 1 nucleus; (6) dysplastic megakaryocytes (≥40?μm) with 2 nuclei; and (7) dysplastic megakaryocytes (≥40?μm) with multiple (more than 2) nuclei. Further, we evaluated the prognostic impact of micro-megakaryocytes and dysplastic mono-nucleated megakaryocytes on MDS patients. The best discriminator cut-off point for each group was determined by the minimal P value approach. In multivariate analyses micro-megakaryocytes?≥25?% and dysplastic mono-nucleated megakaryocytes?≥30?% were independent adverse prognostic factors (hazard ratio [HR]?=?1.58 [95?% confidence interval [CI], 1.11, 2.23]; P?=?0.010 and 1.53 [1.09, 2.16]; P?=?0.014). Our data suggest integration of micro-megakaryocytes and dysplastic mono-nucleated megakaryocytes improve predictive accuracy of the international prognostic scoring system-revised (IPSS-R) scoring system.
机译:Dys-Megakaryopoiesis被世界卫生组织的骨髓涂片中的≥10?百分比巨大的巨型细胞。然而,不同观察者之间消化不良的巨核细胞的一致性率低,因此,对痛经的评估也经常不和谐。我们进行了CD41免疫染色,并提出了骨髓膜上的Dys-Megakaryopoiesis的系统分类:(1)微巨核细胞(<12?μm); (2)微巨核细胞(12-40≤μm),1个核; (3)微巨核细胞(12-40≤μm),2个核; (4)微巨核细胞(12-40μm),多(超过2)核; (5)具有1个核的发育功能性巨核细胞(≥40≤μm); (6)具有2个核的发育功能性巨核细胞(≥40≤μm); (7)具有多个(超过2)个核的发育功能性巨核细胞(≥40≤μm)。此外,我们评估了微巨核细胞和消化障碍单核巨核细胞对MDS患者的预后影响。每组的最佳鉴别器截止点由最小的P值方法确定。在多变量分析中,微巨核细胞?≥25?%和消化塑性单核巨核细胞?≥30?%是独立的不良预后因素(危害比[Hr]?=?1.58 [95],1.11,2.23 ]; p?= 0.010和1.53 [1.09,2.16]; p?= 0.014)。我们的数据表明微巨核细胞和消化性单核巨核细胞的整合提高了国际预后评分系统修订的预测准确性(IPSS-R)评分系统。

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