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XIAP 缺陷的异基因造血细胞移植:国际调查显示预后不良。

Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.

机构信息

Division of Bone Marrow Transplantation and Immunodeficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.

出版信息

Blood. 2013 Feb 7;121(6):877-83. doi: 10.1182/blood-2012-06-432500. Epub 2012 Nov 6.

Abstract

There have been no studies on patient outcome after allogeneic hematopoietic cell transplantation (HCT) in patients with X-linked inhibitor of apoptosis (XIAP) deficiency. To estimate the success of HCT, we conducted an international survey of transplantation outcomes. Data were reported for 19 patients. Seven patients received busulfan-containing myeloablative conditioning (MAC) regimens. Eleven patients underwent reduced intensity conditioning (RIC) regimens predominantly consisting of alemtuzumab, fludarabine, and melphalan. One patient received an intermediate-intensity regimen. Survival was poor in the MAC group, with only 1 patient surviving (14%). Most deaths were from transplantation-related toxicities, including venoocclusive disease and pulmonary hemorrhage. Of the 11 patients who received RIC, 6 are currently surviving at a median of 570 days after HCT (55%). Preparative regimen and HLH activity affected outcomes, and of RIC patients reported to be in remission from HLH, survival is 86% (P = .03). We conclude that MAC regimens should not be used for patients with XIAP deficiency. It is possible that the loss of XIAP and its antiapoptotic functions contributes to the high incidence of toxicities observed with MAC regimens. RIC regimens should be pursued with caution and, if possible, efforts should be made to ensure HLH remission before HCT in these patients.

摘要

目前尚无关于接受异基因造血细胞移植(HCT)的 X 连锁凋亡抑制蛋白(XIAP)缺陷患者的患者结局的研究。为了评估 HCT 的成功,我们对移植结局进行了国际调查。报告了 19 名患者的数据。7 名患者接受了含白消安的清髓性预处理(MAC)方案。11 名患者接受了以阿仑单抗、氟达拉滨和马法兰为主的减低强度预处理(RIC)方案。1 名患者接受了中等强度的预处理方案。MAC 组的生存率较差,只有 1 名患者存活(14%)。大多数死亡是由于与移植相关的毒性,包括静脉闭塞病和肺出血。在接受 RIC 的 11 名患者中,有 6 名在 HCT 后中位时间为 570 天(55%)时仍存活。预处理方案和 HLH 活动影响结局,且报告从 HLH 缓解的 RIC 患者的生存率为 86%(P=0.03)。我们得出结论,MAC 方案不应用于 XIAP 缺陷患者。XIAP 的缺失及其抗凋亡功能可能导致 MAC 方案观察到的毒性发生率增加。RIC 方案应谨慎采用,如果可能,应努力在这些患者进行 HCT 前确保 HLH 缓解。

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