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干细胞移植后威斯科特-奥尔德里奇综合征患者的预后:日本57例患者的分析

Outcome in patients with Wiskott-Aldrich syndrome following stem cell transplantation: an analysis of 57 patients in Japan.

作者信息

Kobayashi Ryoji, Ariga Tadashi, Nonoyama Shigeaki, Kanegane Hirokazu, Tsuchiya Shigeru, Morio Tomohiro, Yabe Hiromasa, Nagatoshi Yoshihisa, Kawa Keisei, Tabuchi Ken, Tsuchida Masahiro, Miyawaki Toshio, Kato Shunichi

机构信息

Department of Paediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

出版信息

Br J Haematol. 2006 Nov;135(3):362-6. doi: 10.1111/j.1365-2141.2006.06297.x.

DOI:10.1111/j.1365-2141.2006.06297.x
PMID:17032176
Abstract

A total of 57 patients with Wiskott-Aldrich syndrome (WAS) were studied after undergoing stem cell transplantation (SCT) in Japan between January 1985 and December 2004. Eleven patients received transplants from human leucocyte antigen (HLA)-matched related donors, 10 from HLA-mismatched related donors, 21 from unrelated bone marrow donors, and 15 from unrelated cord blood donors. Nine of the 57 patients rejected the initial graft. The overall 5-year survival rate was 73.7% and the 5-year failure-free survival rate was 65.7% (failure was defined as rejection or death). The overall 5-year survival rates for patients receiving bone marrow and cord blood from unrelated donors were both 80.0%. Based on univariate analysis, the factors associated with poor survival were: transplantation from an HLA-mismatched related donor, patient age of more than 5 years at the time of transplantation, and a conditioning regimen other than busulfan and cyclophosphamide (BU-CY) or busulfan, cyclophosphamide and antithymocyte globulin (BU-CY-ATG). In a multivariate analysis, a conditioning regimen other than BU-CY and BU-CY-ATG was the only independent factor associated with transplantation failure. Given the improved outcome for WAS patients following transplantation from an unrelated donor, we conclude that patients with WAS should receive SCT as soon as possible after diagnosis.

摘要

1985年1月至2004年12月期间,日本共有57例患有威斯科特-奥尔德里奇综合征(WAS)的患者在接受干细胞移植(SCT)后接受了研究。11例患者接受了来自人类白细胞抗原(HLA)匹配的相关供体的移植,10例来自HLA不匹配的相关供体,21例来自无关骨髓供体,15例来自无关脐血供体。57例患者中有9例排斥了初始移植物。总体5年生存率为73.7%,5年无失败生存率为65.7%(失败定义为排斥或死亡)。接受无关供体骨髓和脐血的患者总体5年生存率均为80.0%。基于单因素分析,与生存不良相关的因素为:来自HLA不匹配相关供体的移植、移植时患者年龄超过5岁以及除白消安和环磷酰胺(BU-CY)或白消安、环磷酰胺和抗胸腺细胞球蛋白(BU-CY-ATG)以外的预处理方案。在多因素分析中,除BU-CY和BU-CY-ATG以外的预处理方案是与移植失败相关的唯一独立因素。鉴于无关供体移植后WAS患者的预后有所改善,我们得出结论,WAS患者应在诊断后尽快接受SCT。

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