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镶嵌型唐氏综合征相关急性髓系白血病在诱导和巩固治疗中并不需要高剂量阿糖胞苷治疗。

Mosaic Down syndrome-associated acute myeloid leukemia does not require high-dose cytarabine treatment for induction and consolidation therapy.

机构信息

Division of Hematology and Oncology, Shizuoka Children's Hospital, Aoi-ku, Shizuoka, Japan.

出版信息

Int J Hematol. 2010 May;91(4):630-5. doi: 10.1007/s12185-010-0549-1. Epub 2010 Mar 18.

Abstract

The present study aimed to identify optimal treatment intensity in children with mosaic Down syndrome (DS) and acute megakaryoblastic leukemia (AMKL). A retrospective review of AMKL patients was undertaken to identify mosaic DS children. Between November 1992 and November 2007, seven children were diagnosed as mosaic DS and AMKL. The median age at diagnosis was 29 months (range 4-34 months). Three patients had a past history of transient abnormal myelopoiesis. UPN1-4 were treated with intermediate-dose cytarabine and UPN4 received additional one course of high-dose cytarabine. All of these patients were remained in first CR. UPN5-7 were treated with high-dose cytarabine according to the AML99 protocol. UPN5 with GATA1 mutation suffered from acute pneumonia and pancreatitis and discontinued chemotherapy. UPN7 relapsed after cessation of chemotherapy and was rescued with allo-PBSCT. The cumulative doses of cytarabine were 3.5-10.65 g/m(2) in the UPN1-4 and 40.4-78.4 g/m(2) in the UPN5-7. The 8-year overall survival was 100% and the 8-year event-free survival 85.7%, respectively. Our retrospective study reveals that patients with mosaic DS and AMKL have a good prognosis. Reduction in intensity may work in patients with mosaic DS as well as with AML-DS.

摘要

本研究旨在确定嵌合体唐氏综合征(DS)和急性巨核细胞白血病(AMKL)患儿的最佳治疗强度。对 AMKL 患者进行回顾性分析以确定嵌合体 DS 患儿。1992 年 11 月至 2007 年 11 月,诊断出 7 例嵌合体 DS 和 AMKL。诊断时的中位年龄为 29 个月(范围 4-34 个月)。3 例有一过性骨髓异常增生史。UPN1-4 采用中剂量阿糖胞苷治疗,UPN4 接受额外 1 个疗程的高剂量阿糖胞苷治疗。所有这些患者均处于首次完全缓解(CR)。UPN5-7 根据 AML99 方案接受高剂量阿糖胞苷治疗。GATA1 突变的 UPN5 发生急性肺炎和胰腺炎,停止化疗。UPN7 化疗停止后复发,采用allo-PBSCT 挽救。UPN1-4 的阿糖胞苷累积剂量为 3.5-10.65g/m(2),UPN5-7 的阿糖胞苷累积剂量为 40.4-78.4g/m(2)。8 年总生存率为 100%,8 年无事件生存率为 85.7%。我们的回顾性研究表明,嵌合体 DS 和 AMKL 患儿预后良好。降低治疗强度可能适用于嵌合体 DS 患者以及 AML-DS 患者。

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