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Status of minimal residual disease determines outcome of autologous hematopoietic SCT in adult ALL.

机译:最小残留疾病的状态决定了成年ALL中自体造血SCT的结果。

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The role of autologous hematopoietic SCT (autoHSCT) in the treatment of high-risk (HR) adult ALL is controversial. In this study, we retrospectively analyzed the results of autoHSCT according to the status of minimal residual disease (MRD) at transplantation, as a joint analysis of the European Study Group for Adult ALL (EWALL). Data on 123 recipients of autoHSCT, aged 31 (16-59) years, with B-lineage (n=77) or T-lineage (n=46) ALL were included. In a cohort of Ph-negative ALL, the probability of leukemia-free survival at 5 years was higher for patients with MRD <0.1% compared with those with MRD > or = 0.1% (57 vs 17%, P=0.0002). The difference was significant for T-lineage ALL (62 vs 8%, P=0.001), and a tendency was observed for B-lineage ALL (54 vs 26%, P=0.17). In a multivariate analysis, adjusted for other potential prognostic factors, high MRD level remained the only independent factor associated with increased risk of failure (risk ratio, 2.8; P=0.0005). We conclude that MRD determines the outcome of autoHSCT in HR adult ALL. Our results suggest the need to reevaluate the role of this treatment option in prospective trials.
机译:自体造血SCT(autoHSCT)在高危(HR)成人ALL治疗中的作用是有争议的。在这项研究中,我们回顾了根据移植时最小残留疾病(MRD)状况对autoHSCT的结果,作为欧洲成人ALL研究组(EWALL)的联合分析。纳入了123名年龄在31(16-59)岁,b谱系(n = 77)或T谱系(n = 46)ALL的autoHSCT受体的数据。在一组Ph阴性ALL患者中,MRD <0.1%的患者5年无白血病存活的可能性高于MRD>或= 0.1%的患者(57比17%,P = 0.0002)。对于T谱系ALL,差异是显着的(62对8%,P = 0.001),并且对于B谱系ALL,存在观察到的趋势(54对26%,P = 0.17)。在多因素分析中,对其他潜在的预后因素进行调整后,高MRD水平仍然是与失败风险增加相关的唯一独立因素(风险比为2.8; P = 0.0005)。我们得出结论,MRD决定了HR成人ALL中autoHSCT的结果。我们的结果表明需要重新评估该治疗方案在前瞻性试验中的作用。

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