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使用氟达拉滨且不进行放疗对具有范可尼贫血(FA)和高风险特征的患者进行异基因造血干细胞移植。

Allogeneic hematopoietic stem cell transplantation of patients with FA and high risk features using fludarabine without radiation.

作者信息

Baker Jillian M, Lewis Victor A, Fernandez Conrad V, Duval Michel, Crooks Bruce N, Yuille Kim, Freedman Melvin H, Doyle John J, Dror Yigal

机构信息

Division of Hematology-Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

出版信息

Pediatr Blood Cancer. 2009 May;52(5):683-5. doi: 10.1002/pbc.21921.

Abstract

Several factors unique to Fanconi anemia (FA) limit the success of allogeneic hematopoietic stem cell transplantation (HSCT) in this population. In this report, we describe a multi-center pilot study of five consecutive FA patients with high-risk features for transplant prepared with fludarabine, without radiation. Four patients engrafted quickly, experienced minimal toxicity and are well at 43-65 months post-transplant. One patient had a C-mismatched unrelated donor transplant and had unsustained engraftment. This fludarabine based regimen without radiation was safe and effective for four high-risk patients, suggesting that eliminating radiation should be further studied as an approach to HSCT in children with FA.

摘要

范可尼贫血(FA)所特有的几个因素限制了该人群中异基因造血干细胞移植(HSCT)的成功率。在本报告中,我们描述了一项多中心试点研究,该研究纳入了连续5例具有移植高风险特征的FA患者,采用氟达拉滨进行预处理,未进行放疗。4例患者迅速植入,毒性极小,移植后43 - 65个月情况良好。1例患者接受了C位点不匹配的无关供体移植,植入未持续。这种基于氟达拉滨且无放疗的方案对4例高风险患者安全有效,这表明应进一步研究消除放疗作为FA患儿HSCT方法的可能性。

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