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使用环磷酰胺、抗胸腺细胞球蛋白和全身照射对重症再生障碍性贫血儿童进行无关供体骨髓移植。

Unrelated donor marrow transplantation in children with severe aplastic anaemia using cyclophosphamide, anti-thymocyte globulin and total body irradiation.

作者信息

Kojima S, Inaba J, Yoshimi A, Takahashi Y, Watanabe N, Kudo K, Horibe K, Maeda N, Kato K, Matsuyama T

机构信息

Department of Developmental Paediatrics, Nagoya University School of Medicine, Nagoya, Japan.

出版信息

Br J Haematol. 2001 Sep;114(3):706-11. doi: 10.1046/j.1365-2141.2001.02992.x.

Abstract

We report a favourable outcome in 15 patients with severe aplastic anaemia (SAA) who were < 20 years of age and who underwent bone marrow transplantation (BMT) from a human leucocyte antigen (HLA)-matched unrelated donor. All patients were non-responders to intensive immunosuppressive therapy (IST) and were multiply transfused. The conditioning regimen consisted of cyclophosphamide (60 mg/kg/d, on d -4 and -3), anti-thymocyte globulin (2.5 mg/kg/d, on d -5 to -2) and total body irradiation (2.5 Gy x 2/d, on d -2 and -1). Patients received cyclosporine and methotrexate for prophylaxis of graft-versus-host disease (GVHD), except for the last four who received tacrolimus instead of cyclosporine. Donor/recipient pairs were identical for HLA class I and II antigens by serological typing, but four pairs were found to have a mismatch at the HLA-A, -B or -DRB1 locus by high-resolution typing. All patients achieved rapid engraftment and are alive at 2-86 months after transplantation (median follow-up, 51 months). Moderate to severe acute GVHD occurred in 5 out of 15 patients (33%); only one patient developed extensive chronic GVHD. Considering our encouraging results, unrelated donor transplantation for SAA is recommended as a salvage therapy in non-responders to IST.

摘要

我们报告了15例年龄小于20岁的重型再生障碍性贫血(SAA)患者的良好治疗结果,这些患者接受了来自人类白细胞抗原(HLA)匹配的无关供者的骨髓移植(BMT)。所有患者对强化免疫抑制治疗(IST)均无反应且多次输血。预处理方案包括环磷酰胺(60mg/kg/d,第-4天和-3天)、抗胸腺细胞球蛋白(2.5mg/kg/d,第-5天至-2天)和全身照射(2.5Gy×2/d,第-2天和-1天)。患者接受环孢素和甲氨蝶呤预防移植物抗宿主病(GVHD),但最后4例患者接受他克莫司代替环孢素。供者/受者对通过血清学分型在HLAⅠ类和Ⅱ类抗原上相同,但通过高分辨率分型发现4对在HLA-A、-B或-DRB1位点存在错配。所有患者均迅速植入,移植后2至86个月存活(中位随访时间为51个月)。15例患者中有5例(33%)发生了中度至重度急性GVHD;只有1例患者发生了广泛的慢性GVHD。鉴于我们令人鼓舞的结果,对于IST无反应者,推荐将无关供者移植作为SAA的挽救治疗方法。

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