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Revised international prognostic scoring system for myelodysplastic syndromes

机译:修订的骨髓增生异常综合症国际预后评分系统

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摘要

The International Prognostic Scoring Sytem (IPSS) is an important standard for ssessing prognosis of primary untreated adult patients with myelodysplastic syndromes (MDS). To refine the IPSS, MDS patient databases from international institutions were coalesced to assemble a much larger combined database (Revised-IPSS [IPSS-R], n = 7012, IPSS, n = 816) for analysis. Multiple statistically weighted clinical features were used to generate a prognostic categorization model. Bone marrow cytogenetics, marrow blast percentage, and cytopenias remained the basis of the new system. Novel components of the current analysis included: 5 rather than 3 cytogenetic prognostic subgroups with specific and new classifications of a number of less common cytogenetic subsets, splitting the low marrow blast percentage value, and depth of cytopenias. This model defined 5 rather than the 4 major prognostic categories that are present in the IPSS. Patient age, performance status, serum ferritin, and lactate dehydrogenase were significant additive features for survival but not for acute myeloid leukemia transformation. This system comprehensively integrated the numerous known clinical features into a method analyzing MDS patient prognosis more precisely than the initial IPSS. As such, this IPSS-R should prove beneficial for predicting the clinical outcomes of untreated MDS patients and aiding design and analysis of clinical trials in this disease.
机译:国际预后评分系统(IPSS)是评估未治疗的成年骨髓增生异常综合征(MDS)成人患者预后的重要标准。为了完善IPSS,合并了国际机构的MDS患者数据库,以建立一个更大的组合数据库(修订版IPSS [IPSS-R],n = 7012,IPSS,n = 816)进行分析。使用多个统计加权的临床特征生成预后分类模型。骨髓细胞遗传学,骨髓胚细胞百分比和血细胞减少症仍然是新系统的基础。当前分析的新组成部分包括:5个而不是3个细胞遗传学预后亚组,具有许多较不常见的细胞遗传学亚组的特定和新分类,将低的骨髓胚细胞百分比值和血细胞减少的深度分开。该模型定义了IPSS中存在的5种而不是4种主要的预后类别。患者的年龄,工作状态,血清铁蛋白和乳酸脱氢酶是存活的重要附加特征,但对于急性髓样白血病转化却没有。与初始IPSS相比,该系统将众多已知的临床特征全面集成到了MDS患者预后的分析方法中。这样,该IPSS-R应该被证明对预测未经治疗的MDS患者的临床结果以及帮助设计和分析该疾病的临床试验是有益的。

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