• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

第二例成人NUTM1融合阳性B细胞淋巴细胞白血病病例:预后不良的反复模式

The second adult case of NUTM1 fusion-positive B-cell lymphoblastic leukemia: A recurring pattern of poor prognosis.

作者信息

Chen Xue, Ma Xiaoli, Yuan Lili, Wang Fang, Zhang Yang, Cao Panxiang, Lu Yue, Chen Jiaqi, Zhou Xiaosu, Liu Hongxing

机构信息

Division of Laboratory Medicine, Hebei Yanda Lu Daopei Hospital, Langfang, 065201, China.

Department of Bone Marrow Transplantation, Hebei Yanda Lu Daopei Hospital, Langfang, 065201, China.

出版信息

Ann Hematol. 2024 Dec;103(12):6041-6043. doi: 10.1007/s00277-024-06115-x. Epub 2024 Nov 25.

DOI:10.1007/s00277-024-06115-x
PMID:39585385
Abstract

This manuscript reports a rare case of CUX1::NUTM1-positive B-cell lymphoblastic leukemia (B-ALL) in a 25-year-old female patient who experienced early relapse and a poor clinical outcome. Given the rarity of NUTM1 fusion-positive B-ALL in adults, this case contributes to the growing evidence that such cases may present with a more aggressive clinical course compared to the pediatric population. Our findings suggest the need for a re-evaluation of therapeutic strategies in adult patients with this subtype of B-ALL.

摘要

本手稿报告了一例罕见的CUX1::NUTM1阳性B细胞淋巴细胞白血病(B-ALL),患者为一名25岁女性,早期复发且临床结局不佳。鉴于成人中NUTM1融合阳性B-ALL罕见,该病例进一步证明,与儿科患者相比,此类病例的临床病程可能更具侵袭性。我们的研究结果表明,需要重新评估成年B-ALL患者这一亚型的治疗策略。

相似文献

1
The second adult case of NUTM1 fusion-positive B-cell lymphoblastic leukemia: A recurring pattern of poor prognosis.第二例成人NUTM1融合阳性B细胞淋巴细胞白血病病例:预后不良的反复模式
Ann Hematol. 2024 Dec;103(12):6041-6043. doi: 10.1007/s00277-024-06115-x. Epub 2024 Nov 25.
2
Prenatal origin of NUTM1 gene rearrangement in infant B-cell precursor acute lymphoblastic leukaemia.婴儿 B 细胞前体急性淋巴细胞白血病中 NUTM1 基因重排的产前起源。
Br J Haematol. 2024 Nov;205(5):1883-1888. doi: 10.1111/bjh.19685. Epub 2024 Aug 5.
3
is a recurrent fusion gene partner in B-cell precursor acute lymphoblastic leukemia associated with increased expression of genes on chromosome band 10p12.31-12.2.是B细胞前体急性淋巴细胞白血病中一种反复出现的融合基因伙伴,与染色体带10p12.31 - 12.2上基因的表达增加相关。
Haematologica. 2019 Oct;104(10):e455-e459. doi: 10.3324/haematol.2018.206961. Epub 2019 Mar 14.
4
Cryptic recurrent ACIN1-NUTM1 fusions in non-KMT2A-rearranged infant acute lymphoblastic leukemia.非 KMT2A 重排婴儿急性淋巴细胞白血病中隐匿性的 ACIN1-NUTM1 融合。
Genes Chromosomes Cancer. 2020 Feb;59(2):125-130. doi: 10.1002/gcc.22808. Epub 2019 Oct 4.
5
The first case of elderly -positive B-cell acute lymphoblastic leukemia.首例老年阳性B细胞急性淋巴细胞白血病病例。
Leuk Lymphoma. 2019 Nov;60(11):2821-2824. doi: 10.1080/10428194.2019.1602267. Epub 2019 May 6.
6
Favorable outcome of NUTM1-rearranged infant and pediatric B cell precursor acute lymphoblastic leukemia in a collaborative international study.一项国际合作研究中NUTM1重排的婴幼儿及儿童B细胞前体急性淋巴细胞白血病的良好预后
Leukemia. 2021 Oct;35(10):2978-2982. doi: 10.1038/s41375-021-01333-y. Epub 2021 Jul 1.
7
MLL/AF-1p fusion in therapy-related early pre-B acute lymphoblastic leukemia with t(1;11)(p32;q23) translocation developing in the relapse phase of acute promyelocytic leukemia.急性早幼粒细胞白血病复发期发生的伴t(1;11)(p32;q23)易位的治疗相关早期前B细胞急性淋巴细胞白血病中的MLL/AF-1p融合
Int J Hematol. 2003 Dec;78(5):439-42. doi: 10.1007/BF02983817.
8
Tumor suppressors BTG1 and IKZF1 cooperate during mouse leukemia development and increase relapse risk in B-cell precursor acute lymphoblastic leukemia patients.肿瘤抑制因子BTG1和IKZF1在小鼠白血病发展过程中协同作用,并增加B细胞前体急性淋巴细胞白血病患者的复发风险。
Haematologica. 2017 Mar;102(3):541-551. doi: 10.3324/haematol.2016.153023. Epub 2016 Dec 15.
9
Relapses and treatment-related events contributed equally to poor prognosis in children with ABL-class fusion positive B-cell acute lymphoblastic leukemia treated according to AIEOP-BFM protocols.根据 AIEOP-BFM 方案治疗的 ABL 类融合阳性 B 细胞急性淋巴细胞白血病患儿,复发和治疗相关事件对预后不良的影响相当。
Haematologica. 2020 Jul;105(7):1887-1894. doi: 10.3324/haematol.2019.231720. Epub 2019 Oct 10.
10
Adult acute lymphoblastic leukemia with near haploidy, hyperdiploidy and Ph positive lines: a rare entity with poor prognosis.具有近单倍体、超二倍体和Ph阳性谱系的成人急性淋巴细胞白血病:一种预后不良的罕见实体。
Leuk Lymphoma. 2006 Mar;47(3):561-3. doi: 10.1080/10428190500361094.

引用本文的文献

1
Narrative review: this or that?-uncommon challenges in mediastinal pathology.叙述性综述:这个还是那个?——纵隔病理学中的罕见挑战
Mediastinum. 2025 Jun 18;9:13. doi: 10.21037/med-25-13. eCollection 2025.

本文引用的文献

1
International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: integrating morphologic, clinical, and genomic data.国际髓系肿瘤和急性白血病分类:整合形态学、临床和基因组数据。
Blood. 2022 Sep 15;140(11):1200-1228. doi: 10.1182/blood.2022015850.
2
The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms.《世界卫生组织造血与淋巴组织肿瘤分类》第五版:淋巴肿瘤。
Leukemia. 2022 Jul;36(7):1720-1748. doi: 10.1038/s41375-022-01620-2. Epub 2022 Jun 22.
3
Two novel cases of NUTM1-rearranged B-cell acute lymphoblastic leukaemia presenting with high-risk features.
两例具有高危特征的NUTM1重排B细胞急性淋巴细胞白血病新病例。
Br J Haematol. 2022 Mar;196(6):1407-1411. doi: 10.1111/bjh.17995. Epub 2021 Dec 12.
4
Favorable outcome of NUTM1-rearranged infant and pediatric B cell precursor acute lymphoblastic leukemia in a collaborative international study.一项国际合作研究中NUTM1重排的婴幼儿及儿童B细胞前体急性淋巴细胞白血病的良好预后
Leukemia. 2021 Oct;35(10):2978-2982. doi: 10.1038/s41375-021-01333-y. Epub 2021 Jul 1.
5
Identification of a novel AVEN-NUTM1 fusion gene in acute myeloid leukemia.急性髓系白血病中一种新型AVEN-NUTM1融合基因的鉴定
Int J Lab Hematol. 2021 Aug;43(4):O207-O210. doi: 10.1111/ijlh.13519. Epub 2021 Mar 23.
6
is a recurrent fusion gene partner in B-cell precursor acute lymphoblastic leukemia associated with increased expression of genes on chromosome band 10p12.31-12.2.是B细胞前体急性淋巴细胞白血病中一种反复出现的融合基因伙伴,与染色体带10p12.31 - 12.2上基因的表达增加相关。
Haematologica. 2019 Oct;104(10):e455-e459. doi: 10.3324/haematol.2018.206961. Epub 2019 Mar 14.