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Myelodysplastic syndrome with chromosome 5 abnormalities: a nationwide survey in Japan

机译:伴有5号染色体异常的骨髓增生异常综合征:日本的全国性调查

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摘要

Chromosome 5 abnormalities, deletion of the long arm of chromosome 5 (del(5q)) or monosomy 5 (-5), arise in about 10% of myelodysplastic syndromes (MDS), either as the sole cytogenetic abnormality or as part of complicated karyotype, and has distinct clinical implications for MDS. However, the prognostic factors of MDS patients with chromosome 5 abnormalities are not determined yet. In this study, 183 Japanese MDS patients with chromosome 5 abnormalities were analyzed. Estimated incidence of del(5q) and 5q- syndrome among MDS patients was 8.4 and 1.3%, respectively. Significant shorter overall survival (OS) and leukemia-free survival (LFS) were observed in -5 patients than del(5q) patients. Among del(5q) patients, addition of monosomy 7 or complex karyotype with more than three abnormalities were significantly related to shorter OS.LFS of del(5q) patients was divided into two risk groups by international prognostic scoring system (IPSS): low/intermediate (Int)-1 and Int-2/high groups. LFS sorted by World Health Organization classification-based prognostic scoring system (WPSS) was also divided into two groups: very low/low/Int and high/very high, and WPSS was able to predict the outcome of del(5q) patients more clearly than IPSS.Together with additional cytogenetic data, WPSS might be useful for clinical decision making in MDS patients with del(5q).
机译:约5%的骨髓增生异常综合征(MDS)中出现5号染色体异常,即5号染色体的长臂缺失(del(5q))或5号单体性(-5),这是唯一的细胞遗传学异常或作为复杂核型的一部分,并且对MDS具有明显的临床意义。然而,MDS患者5号染色体异常的预后因素尚未确定。在这项研究中,分析了183名日本MDS患者的5号染色体异常。 MDS患者中del(5q)和5q-综合征的估计发生率分别为8.4%和1.3%。与del(5q)患者相比,-5患者的总体生存期(OS)和无白血病生存期(LFS)显着缩短。在del(5q)患者中,增加7号单体性或复杂性染色体核型多于三个异常与OS较短有关.del(5q)患者的LFS根据国际预后评分系统(IPSS)分为两个风险组:低/中级(Int)-1和Int-2 / high组。根据世界卫生组织基于分类的预后评分系统(WPSS)排序的LFS也分为两组:极低/低/ Int和高/非常高,并且WPSS能够更清晰地预测del(5q)患者的结果结合其他细胞遗传学数据,WPSS可能对del(5q)的MDS患者的临床决策有用。

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