Shaver Aaron C, Seegmiller Adam C
Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Clin Lab Med. 2017 Dec;37(4):771-785. doi: 10.1016/j.cll.2017.07.005. Epub 2017 Aug 31.
Among the most thoroughly evaluated modalities for assessment of minimal residual disease (MRD) in B acute lymphoblastic leukemia is multiparameter flow cytometry. Flow cytometric evaluation of MRD for B-ALL requires complete understanding of the immunophenotype of hematogones, the normal counterpart of leukemic B lymphoblasts. Assessment of multiple flow cytometry markers, in concert with each other in multidimensional histograms, is necessary to distinguish hematogones from malignant blasts. Emerging therapies targeting CD19 and other B-cell markers can disrupt the most frequently MRD assessment, requiring a revised approach as use of targeted therapies becomes widespread.
多参数流式细胞术是评估B细胞急性淋巴细胞白血病微小残留病(MRD)时评估最为全面的方法之一。对B-ALL的MRD进行流式细胞术评估需要全面了解造血细胞的免疫表型,造血细胞是白血病B淋巴母细胞的正常对应物。在多维直方图中相互配合评估多个流式细胞术标记物,对于区分造血细胞和恶性母细胞是必要的。针对CD19和其他B细胞标记物的新兴疗法可能会干扰最常用的MRD评估方法,随着靶向疗法的广泛应用,需要采用一种修订后的方法。