首页> 外文期刊>Revista Cubana de Hematología, Inmunología y Hemoterapia >Supervivencia de pacientes adultos con leucemia mieloide aguda no promieloc?-tica tratados con altas dosis de antraciclinas
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Supervivencia de pacientes adultos con leucemia mieloide aguda no promieloc?-tica tratados con altas dosis de antraciclinas

机译:成年患者的存活患者急性髓性白血病不是Promieloc? - 用高剂量的蒽环类治疗

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Introduction: Acute myeloid leukemia is a heterogeneous disease characterized by the clonal expansion of undifferentiated precursors that causes bone marrow failure. Objective: To analyze the survival of adult patients with non-promyelocytic acute myeloid leukemia treated with high doses of induced anthracyclines at induction. Methods: An analytical, retrospective and longitudinal study was carried out with 53 adult patients younger than 60 years, treated at the Institute of Hematology and Immunology, from September 2013 to December 2018. These patients had a diagnosis of non-promyelocytic acute myeloid leukemia and received high doses of anthracyclines (daunoribicin) under induction therapy. Results: The probabilities of overall survival at 12 months were higher for the group of 19- 29 years, accounting for 59%, and lower for the group of 40-49 years, accounting for 21%. In the age group of 19-29 years, the probability of event-free survival was 65% and the probability of disease-free survival was 44%. In the group of 40-49 years, it decreased to 27%; while in the group of 50-59 it increased, reaching 80%. Regarding overall survival associated with the rearranged genes, it was higher for the patients who had the NPM1 and AML1-ETO genes and lower for those who had the FLT3 and BCR/ABL genes. Conclusions: Age groups and genetic alterations do not modify the survival of patients with non-promyelocytic acute myeloid leukemias treated with high doses of anthracyclines.
机译:介绍:急性髓性白血病是一种异质疾病,其特征在于未分化的前体的克隆膨胀,导致骨髓衰竭。目的:分析诱导高剂量诱导蒽环瘤治疗非高临性致细胞急性髓性白血病成年患者的存活。方法:分析,回顾性和纵向研究是在2013年9月至2018年12月在血液学和免疫学龄较小的53名成年患者中进行的。这些患者对非幼幼儿织物急性髓性白血病进行了诊断在感应治疗下接受高剂量的蒽环(Daunoribicin)。结果:19至29岁集团的12个月总体存活率的概率较高,占40-49岁组的59%,占,占21%。在19-29岁的年龄组中,无事项存活的可能性为65%,无病生存率的可能性为44%。在40-49岁的小组中,它减少到27%;虽然在50-59组中,它的增加,达到80%。关于与重排基因相关的整体存活,对于具有NPM1和AML1-ETO基因的患者而言,对于那些具有FLT3和BCR / ABL基因的人来说,它较高。结论:年龄组和遗传改变不会改变用高剂量蒽环植物治疗的非幼幼儿织物急性髓性白血病患者的存活。

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