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