首页> 美国卫生研究院文献>Journal of Hematology Oncology >High WT1 expression is an early predictor for relapse in patients with acute promyelocytic leukemia in first remission with negative PML-RARa after anthracycline-based chemotherapy: a single-center cohort study
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High WT1 expression is an early predictor for relapse in patients with acute promyelocytic leukemia in first remission with negative PML-RARa after anthracycline-based chemotherapy: a single-center cohort study

机译:WT1高表达是基于蒽环类药物化疗后首次缓解且PML-RARa阴性的急性早幼粒细胞白血病患者复发的早期预测指标:一项单中心队列研究

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摘要

AbstractWilms’ tumor gene 1 (WT1) expression is a well-known predictor for relapse in acute myeloid leukemia. We monitored WT1 decrement along the treatment course to identify its significant role as a marker for residual disease in acute promyelocytic leukemia (APL) and tried to suggest its significance for relapse prediction. In this single center retrospective study, we serially measured PML-RARa and WT1 expression from 117 APL patients at diagnosis, at post-induction and post-consolidation chemotherapies, and at every 3 months after starting maintenance therapy. All 117 patients were in molecular remission after treatment of at least 2 consolidation chemotherapies. We used WT1 ProfileQuant™ kit (Ipsogen) for WT1 monitoring. High WT1 expression (>120 copies/104 ABL1) after consolidation and at early period (3 months) after maintenance therapy significantly predicted subsequent relapse. All paired PML-RARa RQ-PCR were not detected except for one sample with early relapse. Patients with high WT1 expression at 3 months after maintenance therapy (n = 40) showed a significantly higher relapse rate (30.5 vs. 6.9%, P < 0.001) and inferior disease free survival (62.8 vs. 91.4%, P < 0.001). Multivariate analysis revealed that high peak leukocyte counts at diagnosis (HR = 6.4, P < 0.001) and high WT1 expression at 3 months after maintenance therapy (HR = 7.1, P < 0.001) were significant factors for prediction of relapse. Our data showed high post-remission WT1 expression was a reliable marker for prediction of subsequent molecular relapse in APL. In this high-risk group, early intervention with ATRA ± ATO, anti-CD33 antibody therapy, and WT1-specific therapy may be used for relapse prevention.
机译:摘要Wilms的肿瘤基因1(WT1)表达是急性髓细胞性白血病复发的众所周知的预测因子。我们在整个治疗过程中监测了WT1的递减情况,以确定其在急性早幼粒细胞白血病(APL)中作为残留疾病标志物的重要作用,并试图暗示其对复发预测的意义。在这项单中心回顾性研究中,我们在诊断,诱导后和巩固后化疗以及开始维持治疗后每3个月连续测量了117位APL患者的PML-RARa和WT1表达。治疗至少2例巩固化疗后,所有117例患者均处于分子缓解状态。我们使用WT1 ProfileQuant™试剂盒(Ipsogen)进行WT1监测。巩固治疗后和维持治疗后早期(3个月)WT1高表达(> 120份/ 10 4 ABL1)显着预测了随后的复发。除一个早期复发的样本外,未检测到所有配对的PML-RARa RQ-PCR。维持治疗后3个月WT1表达高的患者(n = 40)表现出明显更高的复发率(30.5 vs. 6.9%,P <0.001)和较低的无病生存期(62.8 vs. 91.4%,P <0.001)。多因素分析显示,诊断时白细胞计数最高峰(HR = 6.4,P WT1 的高表达是预测APL后续分子复发的可靠标志。在这一高危人群中,可以采用ATRA±ATO早期干预,抗CD33抗体疗法和 WT1 特异性疗法来预防复发。

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