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Azacitidine prolongs overall survival and reduces infections and hospitalizations in patients with WHO-defined acute myeloid leukaemia compared with conventional care regimens: an update

机译:与常规护理方案相比阿扎胞苷可延长WHO定义的急性髓细胞性白血病患者的总体存活率并减少感染和住院:最新

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摘要

Azacitidine (AZA), as demonstrated in the phase III trial (AZA-001), is the first MDS treatment to significantly prolong overall survival (OS) in higher risk MDS pts ((2007) Blood >110 817). Approximately, one-third of the patients (pts) enrolled in AZA-001 were FAB RAEB-T (≥20–30% blasts) and now meet the WHO criteria for acute myeloid leukaemia (AML) ((1999) Blood >17 3835). Considering the poor prognosis (median survival <1 year) and the poor response to chemotherapy in these pts, this sub-group analysis evaluated the effects of AZA versus conventional care regimens (CCR) on OS and on response rates in pts with WHO AML.
机译:如III期试验(AZA-001)所述,阿扎胞苷(AZA)是首个可显着延长高危MDS pts总体生存率(OS)的MDS治疗方法((2007)Blood > 110 817 )。大约AZA-001的患者(pts)中有三分之一是FAB RAEB-T(≥20%到30%的胚泡),现在符合WHO的急性髓细胞白血病(AML)标准((1999年)血液> 17 3835)。考虑到这些患者的不良预后(中位生存期<1年)和对化疗的不良反应,本亚组分析评估了AZA与常规护理方案(CCR)对OS和WHO AML患者的OS和缓解率的影响。

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