首页> 外文期刊>Hemoglobin: International Journal for Hemoglobin Research >ALLOGENEIC STEM CELL TRANSPLANTATION IN PATIENTS WITH beta-THALASSEMIA: KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTRE EXPERIENCE
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ALLOGENEIC STEM CELL TRANSPLANTATION IN PATIENTS WITH beta-THALASSEMIA: KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTRE EXPERIENCE

机译:β-地中海贫血患者的同种异体干细胞移植:FAISAL国王专科医院和研究中心的经验

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摘要

From January 1998-July 2006, 62 stem cell transplantation (SCT) were performed on 60 patients with beta-thalassemia from HLA-related match donors. The overall survival (OS) and event free survival (EFS)for all patients were 94 and 77%. The outcome of allogeneic SCT in our experience is satisfactory with OS 92 % and EFS 77%. Transplantation at a young age and when the disease is mild offers the best outcome. More advanced disease is associated with higher rate of rejection and severe graft versus host disease.
机译:从1998年1月至2006年7月,对来自HLA相关比赛供体的60名地中海贫血患者进行了62次干细胞移植(SCT)。所有患者的总生存(OS)和无事件生存(EFS)分别为94%和77%。根据我们的经验,同种异体SCT的结果令人满意,OS为92%,EFS为77%。在年轻时以及疾病轻度时进行移植可获得最佳效果。与宿主疾病相比,更晚期的疾病与更高的排斥率和严重的移植物相关。

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