微小残留病指导的急性髓细胞白血病分层治疗

常英军, 赵晓甦. 微小残留病指导的急性髓细胞白血病分层治疗[J]. 临床血液学杂志, 2023, 36(5): 309-315. doi: 10.13201/j.issn.1004-2806.2023.05.003
引用本文: 常英军, 赵晓甦. 微小残留病指导的急性髓细胞白血病分层治疗[J]. 临床血液学杂志, 2023, 36(5): 309-315. doi: 10.13201/j.issn.1004-2806.2023.05.003
CHANG Yingjun, ZHAO Xiaosu. Minimal residual disease directed therapy for patients with acute myeloid leukemia[J]. J Clin Hematol, 2023, 36(5): 309-315. doi: 10.13201/j.issn.1004-2806.2023.05.003
Citation: CHANG Yingjun, ZHAO Xiaosu. Minimal residual disease directed therapy for patients with acute myeloid leukemia[J]. J Clin Hematol, 2023, 36(5): 309-315. doi: 10.13201/j.issn.1004-2806.2023.05.003

微小残留病指导的急性髓细胞白血病分层治疗

  • 基金项目:
    首都特色重点项目(No:Z221100007422008);国家自然科学基金面上项目(No:82070185)
详细信息
    作者简介:

    常英军,主任医师,二级教授,博士研究生(博士后)导师。科技部重点领域创新团队负责人,2021年入选第六批国家“万人计划”科技创新领军人才;同年获人民名医“优秀风范”称号。现任北京大学医学部血液系主任、北京大学人民医院血液科副主任。中华医学会血液学分分会第十一届委员会委员、实验诊断学组副组长,中华医学会血液学分会第九届、第十届青年委员会副主任委员,美国免疫学会国际会员,海峡两岸医药卫生交流协会血液病学专业委员会第三届委员会副主任委员、中国病理生理学会实验血液学会委员等。承担“863”项目、国家自然科学基金委重大项目子课题、首都特色项目重点课题和京津冀基础研究合作项目等10余项课题。以主要完成人身份获国家科技进步二等奖2项,中华医学科技一等奖2项、二等奖2项及教育部高校科技进步一等奖1项。现为Exp Hematol & Oncol副主编、《白血病·淋巴瘤》副总编辑;J Hematol OncolExpert Rev HematolAdvance in Therapy和《中华血液学杂志》等杂志的编委;任LancetLancet Heamatol等20余种国际杂志的审稿专家。截至目前,以通讯(包括共同通讯)或第一(包括共同第一)作者身份在J Clin OncolBloodCell Discov等国内外学术期刊上发表论文120余篇

    通讯作者: 常英军,E-mail:rmcyj@bjmu.edu.cn
  • 中图分类号: R733.71

Minimal residual disease directed therapy for patients with acute myeloid leukemia

More Information
  • 微小残留病(MRD)已被常规用于急性髓细胞白血病(AML)患者的疗效评估和复发预测。本文从异基因造血干细胞移植适应证、移植方式、预处理方案以及移植后复发预防等方面讨论了MRD指导的个体化分层治疗。未来的研究应聚焦AML患者MRD检测及干预新方法的建立。
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  • 图 1  MRD的概念及其与临床预后的关系

    图 2  MRD指导的AML个体化治疗策略

    表 1  AML患者各种MRD检测方法优缺点比较

    检测方法 敏感性 常规应用 评价
    MFC 10-5~10-3 优点:简便快捷、花费低,适用90%以上的AML患者;缺点:抗原漂移,不能确定特定白血病亚群,分析过程复杂
    RQ-PCR
       融合基因/基因突变 10-6~10-4 优点:特异性好,敏感性高,相对便宜,易标准化;缺点:耗时间,要求靶基因在疾病治疗过程中稳定表达,适用部分患者,RNA不稳定,仅适用30%~60%的患者
       WT1 10-2 优点:适用80%~90%的AML患者;缺点:敏感性低,缺乏疾病特异性
    dd-PCR 10-6~10-4 优点:绝对定量,不需要标准化曲线;缺点:同RQ-PCR
    测序技术
       群体细胞水平 10-6~10-3 优点:可以同时检测多种突变位点,可观察克隆演变,高通量;缺点:花费高,结果易受背景噪音影响,无标准化
       单细胞水平 10-4~10-3 优点:可以同时检测多种突变位点,可在单细胞水平观察克隆演变,可实现单细胞水平同时检测DNA、RNA和表面表型;缺点:花费高,单细胞核酸量有限,结果易受背景噪音影响,无标准化,等位基因遗漏
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出版历程
收稿日期:  2023-03-07
刊出日期:  2023-05-01

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