首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Time from diagnosis to treatment initiation predicts survival in younger, but not older, acute myeloid leukemia patients.
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Time from diagnosis to treatment initiation predicts survival in younger, but not older, acute myeloid leukemia patients.

机译:从诊断到开始治疗的时间可预测较年轻但较不严重的急性髓细胞性白血病患者的存活率。

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摘要

Acute myeloid leukemia (AML) is considered an oncologic emergency. Delaying induction chemotherapy until molecular testing results return, may benefit some patients but harm others. We examined the effect of time from AML diagnosis to treatment (TDT) on complete remission (CR) and overall survival (OS), using patient characteristics available at diagnosis. Regression models were applied to older (> or = 60 years) and younger (< 60 years) adults, controlling for age, baseline white blood cell count, secondary AML (sAML), and performance status. Median patient age was 60 years (range, 17-87 years), TDT 4 days (range, 1-78 days), and 45% had sAML. Cytogenetic risk distribution was: favorable, 8%; intermediate, 66%; unfavorable, 26%. CR rate was 67% and median OS was 68 weeks in patients younger than 60 years; 55% and 33 weeks in older patients, respectively. In univariate and multivariate analyses, longer TDT was associated with worse CR and OS in younger (univariate: P < .001 in both; multivariate: P < .001 and P = .001, respectively), but not older patients (univariate: P = .45, P = .19; multivariate: P = .63, P = .30, respectively). Results did not change with inclusion of cytogenetic data or in risk group subsets. AML therapy should be initiated immediately in younger patients. Delaying treatment does not seem harmful in older patients, allowing individualized approaches.
机译:急性髓细胞性白血病(AML)被认为是一种肿瘤急症。将诱导化疗推迟到分子检测结果恢复之前,可能会使某些患者受益,但对其他患者却会造成伤害。我们使用诊断时可用的患者特征检查了从AML诊断到治疗(TDT)时间对完全缓解(CR)和总体生存(OS)的影响。回归模型适用于年龄较大(>或= 60岁)和年轻人(<60岁)的年龄,基线白细胞计数,继发性AML(sAML)和表现状态。患者年龄中位数为60岁(范围为17-87岁),TDT为4天(范围为1-78天),其中sAML为45%。细胞遗传风险分布为:有利,8%;中级,66%;不利,为26%。 60岁以下患者的CR率为67%,中位OS​​为68周;老年患者分别为55%和33周。在单因素和多因素分析中,较长的TDT与年轻的CR和OS较差相关(单因素:两者均P <.001;多因素:分别为P <.001和P = .001),而老年患者则没有(单因素:P = .45,P = .19;多变量:分别为P = .63,P = .30)。结果未随细胞遗传学数据或危险组亚组的变化而变化。年轻患者应立即开始AML治疗。延迟治疗对老年患者似乎无害,可以采取个体化治疗方法。

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