Bone marrow transplantation for patients with severe aplastic anemia and myelodysplastic syndrome.

S Kai, Y Shinohara
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Abstract

A survey of the results of marrow transplantation for severe aplastic anemia (SAA) and myelodysplastic syndrome (MDS) in Japan is reported. Of the 152 patients with SAA, 109 were alive between 2 and 132 months following transplantation and the probability of survival at 5 years was 70% (for the patients with grafts from HLA-matched siblings) and 100% (for the patients with grafts from monozygous twins). Survival rate at 3 years for the patients with grafts from family members other than HLA-matched siblings was 46%. The chance of survival was influenced by conditioning regimen and recipient's age. Recipients with sustained engraftment had a significantly higher survival rate than those with graft failure (83% vs 11%, p less than 0.001). Since 1985, the results of transplantation from HLA-matched siblings have improved and the 3-year survival is more than 90% for patients under 20 years old. For MDS, the actuarial survival at 3 years was 42%. The chance of survival was not influenced by the FAB classification, patient's age, patient's sex, interval from diagnosis to transplant, karyotype anomaly or graft versus host disease.

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骨髓移植治疗严重再生障碍性贫血和骨髓增生异常综合征。
报道了日本骨髓移植治疗严重再生障碍性贫血(SAA)和骨髓增生异常综合征(MDS)的结果。在152例SAA患者中,109例在移植后2 - 132个月存活,5年生存率为70%(来自hla匹配的兄弟姐妹的患者)和100%(来自同卵双胞胎的患者)。接受家庭成员移植而非hla匹配的兄弟姐妹移植的患者3年生存率为46%。生存机会受调理方案和受者年龄的影响。持续移植的受者的存活率明显高于移植失败的受者(83% vs 11%, p < 0.001)。自1985年以来,来自hla匹配的兄弟姐妹的移植结果有所改善,20岁以下患者的3年生存率超过90%。MDS的3年精算生存率为42%。生存率不受FAB分型、患者年龄、患者性别、诊断至移植间隔、核型异常或移植物抗宿主病的影响。
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The hematopoietic system [Application of nucleolar organizer region staining technique to air-dried blood smears]. [Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells]. [Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia]. [Long-term cultures of marrow cells from the patients with aplastic anemia].
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