Baker Jillian M, Lewis Victor A, Fernandez Conrad V, Duval Michel, Crooks Bruce N, Yuille Kim, Freedman Melvin H, Doyle John J, Dror Yigal
Division of Hematology-Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Pediatr Blood Cancer. 2009 May;52(5):683-5. doi: 10.1002/pbc.21921.
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.
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。