儿童急性淋巴母细胞白血病与唐氏综合征:SHOP/LAL-99和05方案分析

M. García-Bernal , R. Cilveti , M. Villa , J. Molina , R. Fernández-Delgado , I. Badell
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引用次数: 0

摘要

简介和目的唐氏综合症易患儿童白血病。关于急性淋巴细胞白血病(ALL),大多数国际组显示较差的结果相比,非唐氏患者。患者和方法通过本研究,我们分析了在过去十年中接受SHOP(西班牙儿童血液和肿瘤学会)治疗的唐氏综合征患者和18岁以下ALL患者的结果。结果目前从32个中心的1000例患者中获得的数据证实:与急性白血病相关的患者表现出临床和生物学上的低风险治疗,因此可以将其归类为低风险组,因此可以接受中等强度的计划化疗。然而,感染性和毒性并发症的数量大于非唐氏患者,因此总生存期(OS)和无事件生存期(EFS)都受到明显影响。结论未来的目标是优化这些白血病的生物学方面的知识,以确定哪些特征可以采取行动来改善其预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Leucemia aguda linfoblástica infantil y síndrome de Down: análisis de los protocolos SHOP/LAL-99 y 05

Introduction and objective

Down syndrome bears a known predisposition to childhood leukemia. In regards to acute lymphoblastic leukemia (ALL), most international groups show poorer results when compared to non-Down patients.

Patients and methods

With this study we analyze the results obtained with Down syndrome patients and ALL younger than 18 years who were treated with SHOP (Spanish Pediatric Hematology and Oncology Societies) protocols for the past decade.

Results

Current data obtained from 1000 patients out of 32 centers confirm several aspects: those are related to acute leukemia showing clinical and biological low risk treats, thereof they may be categorized in low risk groups hence receive scheduled chemotherapy of moderate intensity. However, the number of infectious and toxic complications is greater than those for non-Down patients, therefore both overall survival (OS) and event free survival (EFS) are markedly affected.

Conclusions

The future aim is to optimize the knowledge on biological aspects of these leukemia, in order to determine those features to be acted upon to improve their outcome.

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