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Karyotype is an independent prognostic parameter in therapy-related acute myeloid leukemia (t-AML): an analysis of 93 patients with t-AML in comparison to 1091 patients with de novo AML

机译:染色体核型是与治疗相关的急性髓细胞性白血病(t-AML)的独立预后参数:对93例t-AML患者和1091例从头AML患者进行分析

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The aim of this study was to compare the pattern of karyotype abnormalities of therapy-related acute myeloid leukemia (t-AML) (n=93) with de novo AML (n=1091), and to evaluate their impact on prognosis. Favorable, intermediate, and unfavorable cytogenetics were observed in 25.8, 28.0, and 46.2% of t-AML, and in 22.2, 57.3, and 20.4% of de novo AML. The median overall survival (OS) was shorter in t-AML than in de novo AML (10 vs 15 months, P=0.0007). Favorable and unfavorable cytogenetics had a prognostic impact with respect to OS in both t-AML (P=0.001 and 0.0001) and de novo AML (PP=0.001 for t-AML, PPP=0.001), while age and WBC count had no impact on OS. In conclusion, these data indicate that cytogenetics are an important prognostic parameter in t-AML. Furthermore, t-AML is an unfavorable factor independent of cytogenetics with respect to survival.
机译:这项研究的目的是比较与治疗相关的急性髓性白血病(t-AML)(n = 93)和新生AML(n = 1091)的核型异常模式,并评估其对预后的影响。在t-AML的25.8%,28.0%和46.2%,以及从头AML的22.2%,57.3%和20.4%中观察到有利,中等和不利的细胞遗传学。 t-AML的中位总体生存期(OS)短于从头AML(10 vs 15个月,P = 0.0007)。良好和不利的细胞遗传学对t-AML(P = 0.001和0.0001)和从头AML(t-AML为PP = 0.001,PPP = 0.001)的OS均对预后有影响,而年龄和WBC计数则无影响在OS上。总之,这些数据表明细胞遗传学是t-AML的重要预后参数。此外,就存活而言,t-AML是独立于细胞遗传学的不利因素。

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