Université de Lille, Unité 1277-Canther, Institut National de la Santé et de la Recherche Médicale (INSERM), Lille, France.
Hematology Laboratory, Centre Hospitalier Universitaire (CHU) de Lille, Lille, France.
Leukemia. 2023 Jun;37(6):1245-1253. doi: 10.1038/s41375-023-01906-z. Epub 2023 Apr 21.
Tandem duplications (TDs) of the UBTF gene have been recently described as a recurrent alteration in pediatric acute myeloid leukemia (AML). Here, by screening 1946 newly diagnosed adult AML, we found that UBTF-TDs occur in about 3% of patients aged 18-60 years, in a mutually exclusive pattern with other known AML subtype-defining alterations. The characteristics of 59 adults with UBTF-TD AML included young age (median 37 years), low bone marrow (BM) blast infiltration (median 25%), and high rates of WT1 mutations (61%), FLT3-ITDs (51%) and trisomy 8 (29%). BM morphology frequently demonstrates dysmyelopoiesis albeit modulated by the co-occurrence of FLT3-ITD. UBTF-TD patients have lower complete remission (CR) rates (57% after 1 course and 76% after 2 courses of intensive chemotherapy [ICT]) than UBTF-wild-type patients. In patients enrolled in the ALFA-0702 study (n = 614 patients including 21 with UBTF-TD AML), the 3-year disease-free survival (DFS) and overall survival of UBTF-TD patients were 42.9% (95%CI: 23.4-78.5%) and 57.1% (95%CI: 39.5-82.8%) and did not significantly differ from those of ELN 2022 intermediate/adverse risk patients. Finally, the study of paired diagnosis and relapsed/refractory AML samples suggests that WT1-mutated clones are frequently selected under ICT. This study supports the recognition of UBTF-TD AML as a new AML entity in adults.
串联重复(TDs)的 UBTF 基因最近被描述为儿科急性髓系白血病(AML)的一种复发性改变。在这里,通过对 1946 例新诊断的成人 AML 进行筛选,我们发现 UBTF-TD 发生在约 3%的 18-60 岁患者中,与其他已知的 AML 亚型定义改变呈相互排斥模式。59 例 UBTF-TD AML 成人患者的特征包括年龄较小(中位数 37 岁)、骨髓(BM)原始细胞浸润程度较低(中位数 25%)、WT1 突变率较高(61%)、FLT3-ITD 率较高(51%)和 8 号染色体三体率较高(29%)。尽管存在 FLT3-ITD 共发生,但 BM 形态学常表现为骨髓发育不良。UBTF-TD 患者完全缓解(CR)率较低(1 个疗程后为 57%,2 个疗程后为 76%强化化疗[ICT])低于 UBTF 野生型患者。在 ALFA-0702 研究(n=614 例患者,包括 21 例 UBTF-TD AML 患者)中,UBTF-TD 患者的 3 年无病生存(DFS)和总生存为 42.9%(95%CI:23.4-78.5%)和 57.1%(95%CI:39.5-82.8%),与 ELN 2022 中危/高危患者无显著差异。最后,配对诊断和复发/难治性 AML 样本的研究表明,WT1 突变克隆在 ICT 下经常被选择。这项研究支持将 UBTF-TD AML 确认为成人 AML 的一种新实体。