• 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

相似文献

1
Hypomethylating agents after allogeneic blood stem cell transplantation.异基因造血干细胞移植后的去甲基化药物
Stem Cell Investig. 2016 Nov 28;3:84. doi: 10.21037/sci.2016.11.04. eCollection 2016.
2
Hypomethylating agents for treatment and prevention of relapse after allogeneic blood stem cell transplantation.用于异基因造血干细胞移植后治疗及预防复发的低甲基化药物。
Int J Hematol. 2018 Feb;107(2):138-150. doi: 10.1007/s12185-017-2364-4. Epub 2017 Nov 15.
3
Treatment of relapsed AML and MDS after allogeneic stem cell transplantation with decitabine and DLI-a retrospective multicenter analysis on behalf of the German Cooperative Transplant Study Group.使用地西他滨和供者淋巴细胞输注治疗异基因干细胞移植后复发的急性髓系白血病和骨髓增生异常综合征——代表德国移植协作研究组的一项回顾性多中心分析
Ann Hematol. 2018 Feb;97(2):335-342. doi: 10.1007/s00277-017-3185-5. Epub 2017 Nov 18.
4
Chemotherapy versus Hypomethylating Agents for the Treatment of Relapsed Acute Myeloid Leukemia and Myelodysplastic Syndrome after Allogeneic Stem Cell Transplant.化疗与去甲基化药物治疗异基因造血干细胞移植后复发的急性髓系白血病和骨髓增生异常综合征的对比
Biol Blood Marrow Transplant. 2016 Jul;22(7):1324-1329. doi: 10.1016/j.bbmt.2016.03.023. Epub 2016 Mar 26.
5
Optimizing outcomes following allogeneic hematopoietic progenitor cell transplantation in AML: the role of hypomethylating agents.优化 AML 患者异基因造血祖细胞移植后的结局:去甲基化药物的作用。
Curr Cancer Drug Targets. 2013 Jul;13(6):661-9. doi: 10.2174/15680096113139990005.
6
Treatment of acute myeloid leukemia or myelodysplastic syndrome relapse after allogeneic stem cell transplantation with azacitidine and donor lymphocyte infusions--a retrospective multicenter analysis from the German Cooperative Transplant Study Group.用阿扎胞苷和供体淋巴细胞输注治疗异基因干细胞移植后急性髓系白血病或骨髓增生异常综合征复发——来自德国移植协作研究组的一项回顾性多中心分析
Biol Blood Marrow Transplant. 2015 Apr;21(4):653-60. doi: 10.1016/j.bbmt.2014.12.016. Epub 2014 Dec 23.
7
Hematopoietic Cell Transplantation in Myelodysplastic Syndromes after Treatment with Hypomethylating Agents.经去甲基化药物治疗后的骨髓增生异常综合征中的造血细胞移植
Biol Blood Marrow Transplant. 2017 Sep;23(9):1509-1514. doi: 10.1016/j.bbmt.2017.05.034. Epub 2017 Jun 30.
8
Optimizing DNA hypomethylating therapy in acute myeloid leukemia and myelodysplastic syndromes.优化急性髓系白血病和骨髓增生异常综合征的 DNA 低甲基化治疗。
Bioessays. 2021 Oct;43(10):e2100125. doi: 10.1002/bies.202100125. Epub 2021 Aug 31.
9
Decitabine in combination with donor lymphocyte infusions can induce remissions in relapsed myeloid malignancies with higher leukemic burden after allogeneic hematopoietic cell transplantation.地西他滨联合供体淋巴细胞输注可使异基因造血细胞移植后白血病负荷较高的复发髓系恶性肿瘤患者获得缓解。
Leuk Res. 2018 Sep;72:20-26. doi: 10.1016/j.leukres.2018.07.005. Epub 2018 Jul 7.
10
Maintenance With Hypomethylating Agents After Allogeneic Stem Cell Transplantation in Acute Myeloid Leukemia and Myelodysplastic Syndrome: A Systematic Review and Meta-Analysis.急性髓系白血病和骨髓增生异常综合征异基因干细胞移植后使用去甲基化药物维持治疗:一项系统评价和荟萃分析。
Front Med (Lausanne). 2022 Feb 15;9:801632. doi: 10.3389/fmed.2022.801632. eCollection 2022.

引用本文的文献

1
Flow cytometry of DNMT1 as a biomarker of hypomethylating therapies.DNA 甲基转移酶 1 的流式细胞术作为低甲基化治疗的生物标志物。
Cytometry B Clin Cytom. 2024 Jan;106(1):11-24. doi: 10.1002/cyto.b.22158. Epub 2024 Feb 12.
2
Generalist in allogeneic hematopoietic stem cell transplantation for MDS or AML: Epigenetic therapy.异基因造血干细胞移植治疗 MDS 或 AML 的通科医生:表观遗传学治疗。
Front Immunol. 2022 Oct 4;13:1034438. doi: 10.3389/fimmu.2022.1034438. eCollection 2022.
3
Prediction of Response and Survival Following Treatment with Azacitidine for Relapse of Acute Myeloid Leukemia and Myelodysplastic Syndromes after Allogeneic Hematopoietic Stem Cell Transplantation.阿扎胞苷治疗异基因造血干细胞移植后急性髓系白血病和骨髓增生异常综合征复发的疗效及生存预测
Cancers (Basel). 2020 Aug 12;12(8):2255. doi: 10.3390/cancers12082255.
4
Clinical applications of donor lymphocyte infusion from an HLA-haploidentical donor: consensus recommendations from the Acute Leukemia Working Party of the EBMT.供者淋巴细胞输注在 HLA 单倍体相合供者中的临床应用:来自 EBMT 急性白血病工作组的共识建议。
Haematologica. 2020 Jan;105(1):47-58. doi: 10.3324/haematol.2019.219790. Epub 2019 Sep 19.
5
[Efficacy of low-dose decitabine in the early relapse of malignant hematological diseases after allogeneic hematopoietic stem cell transplantation].低剂量地西他滨治疗异基因造血干细胞移植后恶性血液病早期复发的疗效
Zhonghua Xue Ye Xue Za Zhi. 2019 Aug 14;40(8):681-684. doi: 10.3760/cma.j.issn.0253-2727.2019.08.011.
6
Management of myelodysplastic syndromes after failure of response to hypomethylating agents.对低甲基化药物反应失败后的骨髓增生异常综合征的管理。
Ther Adv Hematol. 2019 May 9;10:2040620719847059. doi: 10.1177/2040620719847059. eCollection 2019.
7
Minimal residual disease-directed immunotherapy for high-risk myelodysplastic syndrome after allogeneic hematopoietic stem cell transplantation.异基因造血干细胞移植后高危骨髓增生异常综合征微小残留病导向免疫治疗。
Front Med. 2019 Jun;13(3):354-364. doi: 10.1007/s11684-018-0665-5. Epub 2019 Jun 11.
8
Relapse of Acute Myeloid Leukemia after Allogeneic Stem Cell Transplantation: Prevention, Detection, and Treatment.异基因造血干细胞移植后急性髓系白血病的复发:预防、检测和治疗。
Int J Mol Sci. 2019 Jan 8;20(1):228. doi: 10.3390/ijms20010228.
9
Histone deacetylase 6 in cancer.组蛋白去乙酰化酶 6 在癌症中的作用。
J Hematol Oncol. 2018 Sep 3;11(1):111. doi: 10.1186/s13045-018-0654-9.

本文引用的文献

1
Clinical Effects of Driver Somatic Mutations on the Outcomes of Patients With Myelodysplastic Syndromes Treated With Allogeneic Hematopoietic Stem-Cell Transplantation.驱动体细胞突变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预后的临床影响。
J Clin Oncol. 2016 Oct 20;34(30):3627-3637. doi: 10.1200/JCO.2016.67.3616.
2
Phase I study of azacitidine following donor lymphocyte infusion for relapsed acute myeloid leukemia post allogeneic stem cell transplantation.供体淋巴细胞输注后使用阿扎胞苷治疗异基因造血干细胞移植后复发的急性髓系白血病的I期研究。
Leuk Res. 2016 Oct;49:1-6. doi: 10.1016/j.leukres.2016.07.010. Epub 2016 Jul 22.
3
Azacitidine Use After Allogeneic Stem Cell Transplantation-Results From the Polish Adult Leukemia Group.异基因造血干细胞移植后使用阿扎胞苷——来自波兰成人白血病研究组的结果
Transplant Proc. 2016 Jun;48(5):1802-5. doi: 10.1016/j.transproceed.2016.01.078.
4
Clinical activity of azacitidine in patients who relapse after allogeneic stem cell transplantation for acute myeloid leukemia.阿扎胞苷对急性髓系白血病异基因干细胞移植后复发患者的临床活性。
Haematologica. 2016 Jul;101(7):879-83. doi: 10.3324/haematol.2015.140996. Epub 2016 Apr 14.
5
Decitabine+ CAG +DLI in relapsed acute myeloid leukemia after allogeneic stem cell transplantation.地西他滨 + CAG + 供者淋巴细胞输注用于异基因造血干细胞移植后复发的急性髓系白血病
J BUON. 2016 Jan-Feb;21(1):280-1.
6
Model-based adaptive phase I trial design of post-transplant decitabine maintenance in myelodysplastic syndrome.基于模型的骨髓增生异常综合征移植后地西他滨维持治疗的I期适应性试验设计
J Hematol Oncol. 2015 Oct 23;8:118. doi: 10.1186/s13045-015-0208-3.
7
Tolerability and Clinical Activity of Post-Transplantation Azacitidine in Patients Allografted for Acute Myeloid Leukemia Treated on the RICAZA Trial.RICAZA试验中接受急性髓系白血病同种异体移植患者移植后阿扎胞苷的耐受性和临床活性
Biol Blood Marrow Transplant. 2016 Feb;22(2):385-390. doi: 10.1016/j.bbmt.2015.09.004. Epub 2015 Sep 9.
8
Maintenance Therapy with Decitabine after Allogeneic Stem Cell Transplantation for Acute Myelogenous Leukemia and Myelodysplastic Syndrome.急性髓系白血病和骨髓增生异常综合征异基因干细胞移植后使用地西他滨进行维持治疗
Biol Blood Marrow Transplant. 2015 Oct;21(10):1761-9. doi: 10.1016/j.bbmt.2015.05.026. Epub 2015 Jun 5.
9
International phase 3 study of azacitidine vs conventional care regimens in older patients with newly diagnosed AML with >30% blasts.阿扎胞苷对比传统治疗方案用于新诊断的原始细胞比例>30%的老年急性髓系白血病患者的国际3期研究。
Blood. 2015 Jul 16;126(3):291-9. doi: 10.1182/blood-2015-01-621664. Epub 2015 May 18.
10
Hypomethylation and up-regulation of PD-1 in T cells by azacytidine in MDS/AML patients: A rationale for combined targeting of PD-1 and DNA methylation.阿扎胞苷导致骨髓增生异常综合征/急性髓系白血病患者T细胞中PD-1低甲基化及上调:联合靶向PD-1与DNA甲基化的理论依据
Oncotarget. 2015 Apr 20;6(11):9612-26. doi: 10.18632/oncotarget.3324.

异基因造血干细胞移植后的去甲基化药物

Hypomethylating agents after allogeneic blood stem cell transplantation.

作者信息

Schroeder Thomas, Rautenberg Christina, Haas Rainer, Kobbe Guido

机构信息

Department of Hematology, Oncology and Clinical Immunology, University of Duesseldorf, Medical Faculty, Duesseldorf, Germany.

出版信息

Stem Cell Investig. 2016 Nov 28;3:84. doi: 10.21037/sci.2016.11.04. eCollection 2016.

DOI:10.21037/sci.2016.11.04
PMID:28066786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5182210/
Abstract

Allogeneic blood stem cell transplantation (allo-SCT) is a potentially curative treatment for patients with myeloid malignancies such as acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS), but relapse remains the major cause of treatment failure. So far, therapeutic options for patients with AML or MDS who relapse after allo-SCT generally consisted of palliative care, low-dose or intensive chemotherapy as well as cellular therapies such as donor lymphocyte infusions (DLI) and second transplantation in selected cases. Nevertheless, the prognosis of patients with myeloid malignancies relapsing after allo-SCT remains dismal therefore asking for novel treatment strategies. Considering their well-balanced profile of good efficacy and moderate toxicity in the non-transplant setting, the hypomethylating agents (HMA) azacitidine (Aza) and decitabine (DAC) have also been tested either alone or in combination with DLI in the post-transplant period. This review summarizes the current knowledge about the use of these two HMA as pre-emptive, salvage or consolidation therapy mostly retrieved from retrospective studies but also from a few prospective trials. Within this review, we also comment on some practical issues such as optimal dose and schedule, the choice of HMA candidates and the role of additional cellular interventions. Finally, we also give an overview on the assumed mode of actions, ongoing research, clinical studies and potential combination partners aiming to improve this treatment approach.

摘要

异基因造血干细胞移植(allo-SCT)是治疗急性髓系白血病(AML)和骨髓增生异常综合征(MDS)等髓系恶性肿瘤患者的一种潜在治愈性疗法,但复发仍然是治疗失败的主要原因。到目前为止,allo-SCT后复发的AML或MDS患者的治疗选择通常包括姑息治疗、低剂量或强化化疗以及细胞疗法,如供体淋巴细胞输注(DLI),在特定情况下还包括二次移植。然而,allo-SCT后复发的髓系恶性肿瘤患者的预后仍然很差,因此需要新的治疗策略。考虑到它们在非移植环境中疗效良好且毒性适中的平衡特性,去甲基化药物(HMA)阿扎胞苷(Aza)和地西他滨(DAC)也已在移植后单独或与DLI联合进行了测试。本综述总结了目前关于这两种HMA作为抢先、挽救或巩固治疗的应用知识,这些知识大多来自回顾性研究,但也有一些前瞻性试验。在本综述中,我们还对一些实际问题进行了评论,如最佳剂量和给药方案、HMA候选药物的选择以及额外细胞干预的作用。最后,我们还概述了假定的作用方式、正在进行的研究、临床研究以及旨在改进这种治疗方法的潜在联合治疗伙伴。