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急性髓系白血病患儿的预后因素及对缓解诱导治疗的良好反应

Prognostic factors in children with acute myeloid leukaemia and excellent response to remission induction therapy.

作者信息

Karol Seth E, Coustan-Smith Elaine, Cao Xueyuan, Shurtleff Sheila A, Raimondi Susana C, Choi John K, Ribeiro Raul C, Dahl Gary V, Bowman William Paul, Taub Jeffrey W, Degar Barbara, Leung Wing, Downing James R, Pui Ching-Hon, Rubnitz Jeffrey E, Campana Dario, Inaba Hiroto

机构信息

Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.

出版信息

Br J Haematol. 2015 Jan;168(1):94-101. doi: 10.1111/bjh.13107. Epub 2014 Aug 28.

Abstract

Minimal residual disease (MRD) is a strong prognostic factor in children and adolescents with acute myeloid leukaemia (AML) but nearly one-quarter of patients who achieve MRD-negative status still relapse. The adverse prognostic factors among MRD-negative patients remain unknown. We analysed the AML02 study cohort to identify demographic and genetic prognostic factors. Among the presenting features, certain 11q23 abnormalities, such as t(6;11) and t(10;11), acute megakaryoblastic leukaemia without the t(1;22), and age ≥10 years were associated with inferior outcome in patients who had MRD-negative status after either remission induction I or II. By contrast, those with rearrangement of CBF genes had superior outcome. Our study identifies patient populations for whom close post-remission MRD monitoring to detect and treat emerging relapse and adjustment in treatment intensity might be indicated.

摘要

微小残留病(MRD)是儿童和青少年急性髓系白血病(AML)的一个强有力的预后因素,但近四分之一达到MRD阴性状态的患者仍会复发。MRD阴性患者中的不良预后因素尚不清楚。我们分析了AML02研究队列,以确定人口统计学和基因预后因素。在呈现的特征中,某些11q23异常,如t(6;11)和t(10;11)、无t(1;22)的急性巨核细胞白血病以及年龄≥10岁,与诱导缓解I或II后处于MRD阴性状态的患者预后较差相关。相比之下,那些CBF基因重排的患者预后较好。我们的研究确定了哪些患者群体可能需要在缓解后密切进行MRD监测,以检测和治疗新出现的复发情况,并调整治疗强度。

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