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首页> 外文期刊>Annals of Hematology >A prediction model for complete remission upon reinduction for patients with acute myeloid leukemia after failure of anthracycline and cytarabine standard chemotherapy
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A prediction model for complete remission upon reinduction for patients with acute myeloid leukemia after failure of anthracycline and cytarabine standard chemotherapy

机译:蒽环类药物和阿糖胞苷标准化疗失败后急性髓样白血病患者完全缓解后的完全缓解预测模型

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The aim of this study was to investigate clinical parameters that might predict complete remission (CR) following reinduction therapy in patients with acute myeloid leukemia (AML). We retrospectively analyzed outcomes in 142 patients who failed to achieve CR with standard anthracycline-plus-cytarabine induction chemotherapy (IND1) and who received the same regimen as a reduction therapy (IND2). The CR rate after reinduction was 54%. Multivariate analysis showed that the presence of peripheral blood (PB) blasts on the day of commencement of IND2 and ≥20% blasts in an interim BM sample taken during IND1 (C1-INT-BM) were independent risk factors for failure of remission. Our scoring system for prediction of CR after reinduction (CRAR score) included a favorable chromosome risk group, absence of PB blasts on the day of commencement of IND2, and ≤21% blasts in the C1-INT-BM. This scoring system predicted that the rates of CR in the four subgroups would be 92.1%, 68.9%, 29.5%, and 7.3%, respectively, in good agreement with observed CR rates. The CRAR scoring model might be associated with the possibility of achieving CR after reinduction, and may be helpful in choosing alternative strategy for AML patients refractory to standard induction chemotherapy, although further prospective validation is required.
机译:这项研究的目的是研究可预测急性髓细胞性白血病(AML)患者接受减量治疗后的完全缓解(CR)的临床参数。我们回顾性分析了142例标准蒽环类加阿糖胞苷诱导化疗(IND1)无法达到CR且接受与还原疗法(IND2)相同治疗方案的患者的结局。还原后的CR率是54%。多变量分析表明,IND2开始当天存在外周血(PB)爆炸,IND1(C1-INT-BM)期间采集的中期BM样本中爆炸≥20%是缓解失败的独立危险因素。我们用于预测再诱导后CR的评分系统(CRAR评分)包括一个有利的染色体风险组,在IND2开始的当天没有PB原始细胞,以及C1-INT-BM中原始细胞≤21%。该评分系统预测,四个亚组的CR率分别为92.1%,68.9%,29.5%和7.3%,与观察到的CR率非常吻合。尽管需要进一步的前瞻性验证,但CRAR评分模型可能与重新诱导后获得CR的可能性有关,并且可能有助于为难于标准诱导化疗的AML患者选择替代策略。

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