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染色体 7q 缺失对接受异基因造血干细胞移植治疗的骨髓增生异常综合征患者结局的临床影响。

Clinical impact of the loss of chromosome 7q on outcomes of patients with myelodysplastic syndromes treated with allogeneic hematopoietic stem cell transplantation.

机构信息

Department of Hematology, Nagasaki University Hospital, Nagasaki, Japan.

Department of Hematology, Kanazawa University Hospital, Kanazawa, Japan.

出版信息

Bone Marrow Transplant. 2019 Sep;54(9):1471-1481. doi: 10.1038/s41409-019-0469-5. Epub 2019 Feb 4.

DOI:10.1038/s41409-019-0469-5
PMID:30718803
Abstract

We conducted a nationwide retrospective study to evaluate the prognostic influence of +1, der(1;7)(q10;p10) [hereafter der(1;7)] and -7/del(7q) after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for de novo myelodysplastic syndromes (MDS). In this database, 69 MDS patients with der(1;7), 75 with -7/del(7q), and 511 with normal karyotype (NK) underwent allo-HSCT at advanced disease status. The 3-year overall survival (OS) and cumulative incidence of relapse (CIR) were 50.4 and 19.4% for those with der(1;7), 36.2 and 38.4% for -7/del(7q), and 51.1 and 20.7% for NK, respectively. In the multivariate analysis, the presence of -7/del(7q) correlated with a significantly shorter OS (HR [95% CI], 1.38 [1.00-1.89]; P = 0.048) and higher CIR (HR, 2.11 [1.36-3.28]; P = 0.001) than those with NK. There were 23 patients with der(1;7), 29 with -7/del(7q), and 347 with NK who underwent allo-HSCT at early disease status. The 3-year OS and CIR were as follows: 47.3 and 9.5% for the der(1;7) group, 70.5 and 13.8% for -7/del(7q), and 70.9 and 5.6% for NK, respectively. No significant differences were observed in OS and CIR among three groups. The impact of the loss of chromosome 7q on OS and CIR may differ based on its type and disease status after allo-HSCT for MDS.

摘要

我们进行了一项全国性的回顾性研究,以评估 +1、der(1;7)(q10;p10)[以下简称 der(1;7)]和-7/del(7q)在异基因造血干细胞移植(allo-HSCT)治疗新诊断骨髓增生异常综合征(MDS)后的预后影响。在该数据库中,69 例 der(1;7)、75 例-7/del(7q)和 511 例核型正常(NK)的 MDS 患者在疾病进展期接受 allo-HSCT。der(1;7)、-7/del(7q)和 NK 患者的 3 年总生存率(OS)和累积复发率(CIR)分别为 50.4%和 19.4%、36.2%和 38.4%、51.1%和 20.7%。多变量分析显示,-7/del(7q)的存在与 OS 显著缩短相关(HR[95%CI],1.38[1.00-1.89];P=0.048)和 CIR 更高(HR,2.11[1.36-3.28];P=0.001)与 NK 相比。有 23 例 der(1;7)、29 例-7/del(7q)和 347 例 NK 在疾病早期接受 allo-HSCT。3 年 OS 和 CIR 如下:der(1;7)组为 47.3%和 9.5%,-7/del(7q)组为 70.5%和 13.8%,NK 组为 70.9%和 5.6%。三组之间的 OS 和 CIR 无显著差异。染色体 7q 缺失对 OS 和 CIR 的影响可能因 MDS 患者 allo-HSCT 后丢失的类型和疾病状态而异。

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引用本文的文献

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The der(1;7)(q10;p10) defining a distinct profile from -7/del(7q) in myelodysplastic syndromes: A systematic review and meta-analysis.伴有 der(1;7)(q10;p10) 的骨髓增生异常综合征具有独特的 -7/del(7q) 缺失谱:系统评价和荟萃分析。
Cancer Med. 2024 Jan;13(1):e6890. doi: 10.1002/cam4.6890. Epub 2024 Jan 1.
2
Allogeneic transplantation of bone marrow versus peripheral blood stem cells from HLA-identical relatives in patients with myelodysplastic syndromes and oligoblastic acute myeloid leukemia: a propensity score analysis of a nationwide database.异基因骨髓移植与 HLA 完全相合的亲属外周血造血干细胞移植治疗骨髓增生异常综合征和少部分急性髓系白血病患者:全国数据库的倾向性评分分析。
Ann Hematol. 2023 May;102(5):1215-1227. doi: 10.1007/s00277-023-05167-9. Epub 2023 Mar 15.
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Outcomes after allogeneic hematopoietic stem cell transplantation in acute myeloid leukemia patients with der(1;7)(q10;p10).急性髓系白血病伴der(1;7)(q10;p10)患者异基因造血干细胞移植后的结局
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