Department of Hematology/Oncology, Gunma Children's Medical Center, Gunma, Japan.
Department of Pediatrics, Gunma University Graduate School of Medicine, Gunma, Japan.
Genes Chromosomes Cancer. 2023 Apr;62(4):202-209. doi: 10.1002/gcc.23110. Epub 2022 Dec 7.
The prognosis of pediatric acute myeloid leukemia (AML) has improved via stratification therapy. However, relapse or death occurs in 30%-40% of cases. Novel genetic factors for pediatric AML need to be elucidated to improve prognosis. We detected recurrent internal tandem duplication in upstream binding transcription factor (UBTF-ITD) in 1.2% (6/503) of Japanese pediatric patients with de novo AML. No UBTF-ITD was detected in 175 adult patients with AML or in 65 cell lines that included 15 AML, 39 acute lymphoblastic leukemia, five chronic myeloid leukemia, and six neuroblastoma cell lines. All UBTF-ITDs were found in exon 13 and shared a duplicated region. UBTF-ITD was more frequently detected in patients with trisomy 8, FLT3-ITD, WT1 mutation, and/or high PRDM16 expression (trisomy 8, 3/6; FLT3-ITD, 5/6; WT1 mutation, 2/6; and high PRDM16 expression, 6/6). Gene expression patterns of patients with UBTF-ITD were similar to those of patients with NUP98::NSD1 or FUS::ERG. Survival analysis of the AML-05 cohort revealed that patients with UBTF-ITD had worse outcomes than those without UBTF-ITD (3-year event-free survival, 20% vs. 55%; 3-year overall survival, 40% vs. 74%). Moreover, among the 27 patients with trisomy 8, all three patients with UBTF -ITD had a poor prognosis resulting in early events (relapse or non-complete remission) within 1 year. Our findings suggest that UBTF-ITD may be a novel and significant prognostic factor for pediatric patients with AML.
通过分层治疗,儿童急性髓系白血病(AML)的预后有所改善。然而,仍有 30%-40%的病例会出现复发或死亡。需要阐明儿童 AML 的新遗传因素以改善预后。我们在 1.2%(6/503)的日本初发儿童 AML 患者中检测到上游结合转录因子(UBTF)内串联重复,在 175 例成人 AML 患者或包括 15 例 AML、39 例急性淋巴细胞白血病、5 例慢性髓性白血病和 6 例神经母细胞瘤细胞系在内的 65 个细胞系中均未检测到 UBTF-ITD。所有 UBTF-ITD 均位于外显子 13 中,并共享一个重复区域。UBTF-ITD 在伴有三体 8、FLT3-ITD、WT1 突变和/或高 PRDM16 表达的患者中更常被检出(三体 8,3/6;FLT3-ITD,5/6;WT1 突变,2/6;高 PRDM16 表达,6/6)。携带 UBTF-ITD 的患者的基因表达模式与 NUP98::NSD1 或 FUS::ERG 患者相似。AML-05 队列的生存分析显示,携带 UBTF-ITD 的患者预后较无 UBTF-ITD 的患者差(3 年无事件生存率,20%比 55%;3 年总生存率,40%比 74%)。此外,在 27 例伴有三体 8 的患者中,所有 3 例携带 UBTF-ITD 的患者预后均较差,在 1 年内均发生早期事件(复发或非完全缓解)。我们的研究结果表明,UBTF-ITD 可能是儿童 AML 患者的一个新的重要预后因素。