Suppr超能文献

伴有 t(6;9)(p23;q34);DEK-NUP214 的 AML 患者行异基因造血干细胞移植时,在首次完全缓解期进行移植具有较好的疗效。

Allogeneic stem cell transplantation in AML with t(6;9)(p23;q34);DEK-NUP214 shows a favourable outcome when performed in first complete remission.

机构信息

Hematology Department, Hospital Clínic of Barcelona, Barcelona, Spain.

IDIBAPS, Josep Carreras Leukemia Research Institute, Barcelona, Spain.

出版信息

Br J Haematol. 2020 Jun;189(5):920-925. doi: 10.1111/bjh.16433. Epub 2020 Feb 5.

Abstract

Acute myeloid leukaemia (AML) with t(6;9)(p23;q34) is a poor-risk entity, commonly associated with FLT3-ITD (internal tandem duplication). Allogeneic stem-cell tranplantation (allo-SCT) is recommended, although studies analysing the outcome of allo-SCT in this setting are lacking. We selected 195 patients with t(6;9) AML, who received a first allo-SCT between 2000 and 2016 from the EBMT (European Society for Blood and Marrow Transplantation) registry. Disease status at time of allo-SCT was the strongest independent prognostic factor, with a two-year leukaemia-free survival and relapse incidence of 57% and 19% in patients in CR1 (first complete remission), 34% and 33% in CR2 (second complete remission), and 24% and 49% in patients not in remission, respectively (P < 0·001). This study, which represents the largest one available in t(6;9) AML, supports the recommendation to submit these patients to allo-SCT in CR1.

摘要

伴有 t(6;9)(p23;q34)的急性髓系白血病(AML)是一种预后不良的疾病,通常与 FLT3-ITD(内部串联重复)相关。建议进行异基因造血干细胞移植(allo-SCT),尽管缺乏分析这种情况下 allo-SCT 结果的研究。我们从 EBMT(欧洲血液和骨髓移植学会)登记处选择了 195 例患有 t(6;9)AML 的患者,他们在 2000 年至 2016 年期间接受了第一次 allo-SCT。allo-SCT 时的疾病状态是最强的独立预后因素,分别在 CR1(第一次完全缓解)、CR2(第二次完全缓解)和未缓解的患者中,两年无白血病生存率和复发率分别为 57%和 19%、34%和 33%以及 24%和 49%(P<0·001)。这项研究代表了 t(6;9)AML 中最大的一项研究,支持将这些患者推荐至 CR1 进行 allo-SCT。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验