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A favorable inductive remission rate for decitabine combined with chemotherapy as a first course in 60‐year‐old acute myeloid leukemia patients with myelodysplasia syndrome features

机译:60岁的急性髓样增生综合征的急性髓细胞白血病患者以地西他滨与化学疗法相结合的诱导缓解率作为首选疗程

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摘要

In acute myeloid leukemia (AML), myelodysplasia‐related changes contribute to a poor prognosis. This retrospective, propensity score‐matched study analyzed 108 newly diagnosed AML patients with features of myelodysplasia syndrome (MDS) (aged 14‐60 years) from 2014 to 2018, who received either idarubicin and cytarabine (IA) or decitabine, idarubicin and cytarabine (DAC+IA), and compared efficacy and toxicity between the two regimens. After propensity score matching, there were 54 patients in each group. The rate of complete remission (CR) was higher in the DAC+IA group than in the IA group (85.2% vs 68.5%, P = .040) after the first course, and toxicities were comparable in both groups. Multivariate analysis indicated that the combination with DAC was independent factor for CR rate after the first induction therapy (OR = 2.978, 95% CI:1.090‐8.137, P = .033). Subgroup analysis showed a CR advantage for DAC+IA (vs IA) for patients of intermediate‐high risk status according to National Comprehensive Cancer Network prognostic stratification. In conclusion, DAC+IA is therefore offered as a new induction choice for newly diagnosed AML patients with features of MDS, aged <60 years old, especially in intermediate‐high risk status.
机译:在急性髓细胞性白血病(AML)中,与骨髓增生异常相关的变化会导致不良的预后。这项回顾性倾向得分匹配的研究分析了2014年至2018年间108例具有骨髓增生异常综合征(MDS)特征的新诊断AML患者(年龄14-60岁),他们接受了伊达比星和阿糖胞苷(IA)或地西他滨,伊达比星和阿糖胞苷( DAC + IA),并比较了两种方案的疗效和毒性。倾向评分匹配后,每组54例。首次疗程后,DAC + IA组的完全缓解率(CR)高于IA组(85.2%vs 68.5%,P = .040),并且两组毒性均相当。多变量分析表明,与DAC的组合是首次诱导治疗后CR率的独立因素(OR = 2.978,95%CI:1.090-8.137,P = .033)。根据国家综合癌症网络的预后分层,亚组分析显示,对于中高危状态患者,DAC + IA(vs IA)具有CR优势。总之,因此,DAC + IA可作为新诊断的具有MDS特征的AML患者的新选择,这些患者年龄小于60岁,尤其是处于中高风险状态。

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