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急性淋巴细胞白血病患儿首次缓解期的诱导死亡及治疗相关死亡率:基于奥地利柏林-法兰克福-明斯特研究组的人群分析

Induction death and treatment-related mortality in first remission of children with acute lymphoblastic leukemia: a population-based analysis of the Austrian Berlin-Frankfurt-Münster study group.

作者信息

Prucker C, Attarbaschi A, Peters C, Dworzak M N, Pötschger U, Urban C, Fink F-M, Meister B, Schmitt K, Haas O A, Gadner H, Mann G

机构信息

Department of Paediatric Haematology and Oncology, St Anna Children's Hospital, Vienna, Austria.

出版信息

Leukemia. 2009 Jul;23(7):1264-9. doi: 10.1038/leu.2009.12. Epub 2009 Feb 12.

Abstract

In the management of the childhood acute lymphoblastic leukemia (ALL), 5% of failures are due to induction death and treatment-related deaths in first complete remission. We retrospectively analyzed the incidence, pattern and causes of death and its risk factors for 896 children with ALL enrolled into five Austrian (A) Berlin-Frankfurt-Münster (BFM) trials between 1981 and 1999. The estimated 10-year cumulative incidence of death significantly decreased from 6+/-1% (n=16/268) in trials ALL-BFM-A 81 and ALL-A 84 to 2+/-1% (n=15/628) in trials ALL-BFM-A 86, 90 and 95 (P=0.006). A significant reduction of death was evident during induction therapy (2.2% in trials ALL-BFM-A 81 and ALL-A 84 and 0.2% in trials ALL-BFM-A 86, 90 and 95, P=0.001). Of 31 patients, 21 (68%) patients died from infectious and 10 (32%) from noninfectious complications. Treatment in trial ALL-BFM-A 81, infant age and female gender were independent predictors of an enhanced risk for death. Conclusively, we found a progressive reduction of death rates that may be explained by the increasing experience in specialized hemato-oncologic centers and improved supportive and intensive care. We also identified a distinct subset of patients who are especially prone to death and may need a special focus when receiving intense chemotherapy.

摘要

在儿童急性淋巴细胞白血病(ALL)的治疗中,5%的治疗失败是由于诱导期死亡和首次完全缓解期与治疗相关的死亡。我们回顾性分析了1981年至1999年间纳入奥地利5项柏林-法兰克福-明斯特(BFM)试验的896例ALL患儿的死亡发生率、模式、原因及其危险因素。估计的10年累积死亡率从ALL-BFM-A 81和ALL-A 84试验中的6±1%(n = 16/268)显著下降至ALL-BFM-A 86、90和95试验中的2±1%(n = 15/628)(P = 0.006)。诱导治疗期间死亡显著减少(ALL-BFM-A 81和ALL-A 84试验中为2.2%,ALL-BFM-A 86、90和95试验中为0.2%,P = 0.001)。在31例死亡患者中,21例(68%)死于感染性并发症,10例(32%)死于非感染性并发症。ALL-BFM-A 81试验中的治疗、婴儿年龄和女性性别是死亡风险增加的独立预测因素。总之,我们发现死亡率逐渐降低,这可能是由于专业血液肿瘤中心经验的增加以及支持治疗和重症监护的改善。我们还确定了一个特别容易死亡的患者亚组,在接受强化化疗时可能需要特别关注。

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