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对于11名接受急性白血病造血干细胞移植的唐氏综合征患儿,治疗失败的主要原因是复发,而非方案相关毒性。

Relapse, not regimen-related toxicity, was the major cause of treatment failure in 11 children with Down syndrome undergoing haematopoietic stem cell transplantation for acute leukaemia.

作者信息

Meissner B, Borkhardt A, Dilloo D, Fuchs D, Friedrich W, Handgretinger R, Peters C, Schrauder A, Schuster F R, Vormoor J, Maecker B, Sykora K W, Zintl F, Welte K, Sauer M

机构信息

Department of Paediatric Haematology and Oncology, Hannover Medical School, Hannover, Germany.

出版信息

Bone Marrow Transplant. 2007 Nov;40(10):945-9. doi: 10.1038/sj.bmt.1705844. Epub 2007 Sep 3.

Abstract

We report a retrospective analysis of 11 children with Down syndrome (DS) treated by SCT in eight German/Austrian SCT centres. Indications for transplantation were acute lymphoblastic leukaemia (N=8) and acute myeloid leukaemia (N=3). A reduced intensity conditioning (RIC) containing 2 Gy TBI was given to two patients, another five received a myeloablative regimen with 12 Gy TBI. Treosulphan or busulphan was used in the remaining four children. Four of eleven (36%) patients are alive. All of them were treated with a myeloablative regimen. One of the four surviving children relapsed 9 months after SCT and is currently receiving palliative outpatient treatment. The main cause of death was relapse (5/11). Two children died of regimen-related toxicity (RRT), one from severe exfoliative dermatitis and multiorgan failure after a treosulphan-containing regimen, the other from GvHD-related infections after RIC. Acute GvHD of the skin was observed in 10 of 10 evaluable patients, and chronic GvHD in 4 of 8. Our data show that DS patients can tolerate commonly used, fully myeloablative preparative regimens. The major cause of death is relapse rather than RRT resulting in an event-free survival of 18% and over all survival of 36%.

摘要

我们报告了对11名唐氏综合征(DS)患儿进行回顾性分析的结果,这些患儿在德国/奥地利的8个造血干细胞移植(SCT)中心接受了治疗。移植指征为急性淋巴细胞白血病(n = 8)和急性髓细胞白血病(n = 3)。两名患者接受了含2 Gy全身照射(TBI)的减低强度预处理(RIC),另外五名患者接受了12 Gy TBI的清髓性方案。其余四名儿童使用了曲奥舒凡或白消安。11名患者中有4名(36%)存活。他们均接受了清髓性方案治疗。四名存活儿童中有一名在SCT后9个月复发,目前正在接受姑息性门诊治疗。主要死亡原因是复发(5/11)。两名儿童死于方案相关毒性(RRT),一名死于含曲奥舒凡方案后的严重剥脱性皮炎和多器官功能衰竭,另一名死于RIC后的移植物抗宿主病(GvHD)相关感染。10名可评估患者中有10名出现皮肤急性GvHD,8名中有4名出现慢性GvHD。我们的数据表明,DS患者能够耐受常用的、完全清髓性的预处理方案。主要死亡原因是复发而非RRT,无事件生存率为18%,总生存率为36%。

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