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31例异基因造血干细胞移植患者疗效观察 被引量:1

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摘要 目的:观察异基因造血干细胞移植治疗恶性血液病的临床疗效。方法:选取住院接受异基因移植患者31例,采用改良马利兰/环磷酰胺(Bu/Cy)方案预处理,对移植后造血重建、移植物抗宿主病(GVHD)及生存率进行分析。结果:31例患者全部植活,100%获造血重建,GVHD发生率为19.4%,移植后100 d内移植相关死亡率为3.2%,移植后100 d无病存活率为96.8%,移植后100 d~1年内移植相关死亡率为10%。结论:造血干细胞移植是目前治疗恶性血液病有效的治疗手段。
出处 《贵阳医学院学报》 CAS 2011年第6期646-648,共3页 Journal of Guiyang Medical College
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