Suppr超能文献

德国移植中心关于范可尼贫血造血干细胞移植的共识

Consensus of German transplant centers on hematopoietic stem cell transplantation in Fanconi anemia.

作者信息

Chao M M, Ebell W, Bader P, Beier R, Burkhardt B, Feuchtinger T, Handgretinger R, Hanenberg H, Koehl U, Kratz C, Kremens B, Lang P, Meisel R, Mueller I, Roessig C, Sauer M, Schlegel P G, Schulz A, Strahm B, Thol F, Sykora K W

机构信息

Pediatric Hematology/Oncology, Hannover Medical School, Hannover, Germany.

Pediatric Hematology/Oncology and Stem Cell Transplantation, Charité University Medicine Berlin, Berlin, Germany.

出版信息

Klin Padiatr. 2015 May;227(3):157-65. doi: 10.1055/s-0035-1548841. Epub 2015 May 18.

Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is currently the only curative therapy for the severe hematopoietic complications associated with Fanconi anemia (FA). In Germany, it is estimated that 10-15 transplants are performed annually for FA. However, because FA is a DNA repair disorder, standard conditioning regimens confer a high risk of excessive regimen-related toxicities and mortality, and reduced intensity regimens are linked with graft failure in some FA patients. Moreover, development of graft-versus-host disease is a major contributing factor for secondary solid tumors. The relative rarity of the disorder limits HSCT experience at any single center. Consensus meetings were convened to develop a national approach for HSCT in FA. This manuscript outlines current experience and knowledge about HSCT in FA and, based on this analysis, general recommendations reached at these meetings.

摘要

异基因造血干细胞移植(HSCT)目前是治疗与范可尼贫血(FA)相关的严重造血并发症的唯一治愈性疗法。在德国,据估计每年进行10 - 15例FA患者的移植手术。然而,由于FA是一种DNA修复障碍疾病,标准预处理方案会带来与方案相关的过度毒性和死亡的高风险,而降低强度的预处理方案在一些FA患者中与移植失败有关。此外,移植物抗宿主病的发生是继发性实体瘤的一个主要促成因素。该疾病相对罕见限制了任何单一中心的HSCT经验。为此召开了共识会议,以制定FA患者HSCT的全国性方法。本手稿概述了目前关于FA患者HSCT的经验和知识,并基于此分析,阐述了这些会议达成的一般性建议。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验