Papadopoulou Vasiliki, Schiavini Giulia, Stalder Gregoire, Basset Valentin, Schoumans Jacqueline, Nabergoj Mitja, Schaller Muriel
Hematology Service and Laboratory, Department of Oncology, Lausanne University Hospital, 1011 Lausanne, Switzerland.
Hematology Service, Department of Oncology, Cantonal Hospital of Valais, 1951 Sion, Switzerland.
Biomedicines. 2024 Oct 9;12(10):2282. doi: 10.3390/biomedicines12102282.
AML with mutation is the largest subcategory of AML, representing about 35% of AML cases. It is characterized by CD34 negativity, which suggests a relatively differentiated state of the bulk of leukemic blasts. Notably, a significant subset of NPM1-mutated AML cases also exhibit HLA-DR negativity, classifying them as "double-negative", and mimicking, therefore, the CD34 HLA-DR immunophenotype of acute promyelocytic leukemia (APL). This study focuses on the "acute promyelocytic leukemia-like" ("APL-like") subset of NPM1-mutated AML, which can be challenging to distinguish from APL at presentation, prior to confirming RARa translocations. We aim to investigate the hematologic and immunophenotypic parameters that may aid to its distinction from APL. Additionally, we explore differences in genetic profile and prognosis between "APL-like" and "non-APL-like" NPM1-mutated AML cases. We conducted a retrospective evaluation of 77 NPM1-mutated AML cases and 28 APL cases. Morphological characteristics, hematologic parameters (such as DD/WBC and PT/WBC), and specific immunophenotypic markers (including SSC, CD64, and CD4) can assist in the early distinction of "APL-like" NPM1-mutated AML from APL. Regarding differences in genetic profiles and outcomes between "APL-like" and non-"APL-like" NPM1-mutated AML cases, we observed a significantly higher incidence of IDH1/2 /TET2 mutations, along with a significantly lower incidence of DNMT3A mutations in the "APL-like" subset compared to the non-"APL-like" subset. The frequency of Ras-pathway and FLT3 mutations did not differ between these last two groups, nor did their prognoses. Our findings contribute to a comprehensive characterization of NPM1-mutated AML, enhancing diagnostic accuracy and aiding in the detailed classification of the disease. This information may potentially guide targeted therapies or differentiation-based treatment strategies.
伴有 突变的急性髓系白血病(AML)是AML中最大的亚类,约占AML病例的35%。其特征为CD34阴性,这表明大部分白血病原始细胞处于相对分化状态。值得注意的是,相当一部分NPM1突变的AML病例也表现出HLA - DR阴性,将它们归类为“双阴性”,因此类似于急性早幼粒细胞白血病(APL)的CD34 HLA - DR免疫表型。本研究聚焦于NPM1突变AML的“急性早幼粒细胞白血病样”(“APL样”)亚类,在确认RARa易位之前,该亚类在初诊时可能难以与APL区分。我们旨在研究有助于将其与APL区分的血液学和免疫表型参数。此外,我们还探讨了“APL样”和“非APL样”NPM1突变AML病例在基因谱和预后方面的差异。我们对77例NPM1突变的AML病例和28例APL病例进行了回顾性评估。形态学特征、血液学参数(如DD/WBC和PT/WBC)以及特定的免疫表型标志物(包括SSC、CD64和CD4)有助于早期将“APL样”NPM1突变的AML与APL区分开来。关于“APL样”和非“APL样”NPM1突变AML病例在基因谱和预后方面的差异,我们观察到与非“APL样”亚类相比,“APL样”亚类中IDH1/2 /TET2基因突变的发生率显著更高,而DNMT3A基因突变的发生率显著更低。最后这两组之间Ras通路和FLT3基因突变的频率以及它们的预后并无差异。我们的研究结果有助于对NPM1突变的AML进行全面表征,提高诊断准确性并有助于对该疾病进行详细分类。这些信息可能潜在地指导靶向治疗或基于分化的治疗策略。