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慢性粒单核细胞白血病白血病转化的表型亚型。

Phenotypic subtypes of leukaemic transformation in chronic myelomonocytic leukaemia.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

Br J Haematol. 2023 Nov;203(4):581-592. doi: 10.1111/bjh.19060. Epub 2023 Aug 22.

Abstract

Chronic myelomonocytic leukaemia (CMML) is a haematological disorder with high risk of transformation to acute myeloid leukaemia (AML). To characterize the phenotypic and genomic patterns of CMML progression, we evaluated a cohort of 189 patients with AML evolving from CMML. We found that transformation occurs through distinct trajectories characterized by genomic profiles and clonal evolution: monocytic (Mo-AML, 53%), immature myeloid (My-AML, 43%) or erythroid (Ery-AML, 2%). Mo-AML, characterized by expansion of monoblasts and promonocytes (low CD34, CD117 expression; high CD14, CD33, CD56 and CD64 expression), were defined by SRSF2, TET2 and RAS pathway mutation co-dominance and were more likely to evolve from SRSF2-TET2 co-mutant CMML through emergence/expansion of RAS pathway mutant clones. Conversely, My-AML, characterized by expansion of immature myeloid blasts (high frequency of CD34, CD38, CD117; low frequency of CD14, CD64 and CD56 expression) were less likely to exhibit SRSF2-TET2 co-mutations or RAS pathway mutations and had higher frequency of CEBPA mutations. Ery-AML was defined by complex karyotypes and TP53 mutations. A trend towards improved OS and EFS with hypomethylating agent-venetoclax combination was observed in My-AML, but not Mo-AML. These findings define distinct progression of CMML and set the basis for future studies evaluating the role of phenotype-specific therapeutics.

摘要

慢性粒单核细胞白血病 (CMML) 是一种具有向急性髓系白血病 (AML) 转化高风险的血液系统疾病。为了描述 CMML 进展的表型和基因组模式,我们评估了一组 189 例由 CMML 演变而来的 AML 患者。我们发现,转化通过具有基因组特征和克隆进化的不同轨迹发生:单核细胞(Mo-AML,53%)、未成熟髓系(My-AML,43%)或红细胞(Ery-AML,2%)。Mo-AML 的特征是原始单核细胞和前单核细胞的扩增(低 CD34、CD117 表达;高 CD14、CD33、CD56 和 CD64 表达),由 SRSF2、TET2 和 RAS 通路突变共显性定义,并且更有可能通过 SRSF2-TET2 共突变 CMML 通过 RAS 通路突变克隆的出现/扩增而演变。相反,My-AML 的特征是未成熟髓系原始细胞的扩增(高频率的 CD34、CD38、CD117;低频率的 CD14、CD64 和 CD56 表达),不太可能表现出 SRSF2-TET2 共突变或 RAS 通路突变,并且 CEBPA 突变的频率更高。Ery-AML 由复杂的核型和 TP53 突变定义。在 My-AML 中观察到与低甲基化剂维奈托克联合应用的 OS 和 EFS 改善趋势,但在 Mo-AML 中未观察到。这些发现定义了 CMML 的不同进展,并为未来评估表型特异性治疗作用的研究奠定了基础。

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