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异基因造血干细胞移植治疗无原始细胞过多骨髓增生异常综合征91例临床分析

Outcomes of allogeneic hematopoietic stem cell transplantation for myelodysplastic syndrome without excess blasts
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摘要 骨髓增生异常综合征(MDS)是以病态造血、外周血细胞减少为主要特征的克隆性血液系统疾病[1]。较低危组MDS患者的主要治疗目标是纠正血细胞减低、减轻输血依赖、延缓疾病进展以及改善生活质量[2]。这部分患者主要接受促红细胞生成素(EPO)、来那度胺(LEN)、去甲基化药物(HMA)、免疫抑制剂等药物治疗,合并严重血细胞减少、经其他治疗无效的患者推荐异基因造血干细胞移植(allo-HSCT),但针对血细胞减低、较低危组MDS患者移植治疗的报道不多,allo-HSCT后的疗效及预后影响因素尚不明确[3]。亲缘全相合造血干细胞移植(MRD-HSCT)、非亲缘全相合造血干细胞移植(MUD-HSCT)、单倍型造血干细胞移植(haplo-HSCT)治疗较高危组MDS的疗效接近[4,5,6],国内暂时缺乏较低危组MDS患者相关报道。本研究对91例接受allo-HSCT的无原始细胞过多MDS患者进行回顾性分析。
作者 俞瑜 张晓辉 王昱 陈欢 韩伟 陈瑶 张圆圆 陈育红 莫晓冬 付海霞 闫晨华 孙于谦 王峰蓉 王景枝 刘开彦 黄晓军 许兰平 Yu Yu;Zhang Xiaohui;Wang Yu;Chen Huan;Han Wei;Chen Yao;Zhang Yuanyuan;Chen Yuhong;Mo Xiaodong;Fu Haixia;Yan Chenhua;Sun Yuqian;Wang Fengrong;Wang Jingzhi;Liu Kaiyan;Huang Xiaojun;Xu Lanping(Peking University People’s Hospital,Peking University Institute of Hematology,Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation for Hematological Diseases,Beijing 100044,China)
出处 《中华血液学杂志》 CAS CSCD 北大核心 2020年第10期861-864,共4页 Chinese Journal of Hematology
基金 国家自然科学基金(81670167、81530046、81621001)。
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