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2
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[Progress of research on allogeneic hematopoietic stem cell transplantation with reduced-intensity conditioning regimen for treatment of myelodysplastic syndrome - review].[减低强度预处理异基因造血干细胞移植治疗骨髓增生异常综合征的研究进展 - 综述]
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Am Soc Clin Oncol Educ Book. 2015:e398-412. doi: 10.14694/EdBook_AM.2015.35.e398.
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Retrospective comparison of reduced-intensity conditioning and conventional high-dose conditioning for allogeneic hematopoietic stem cell transplantation using HLA-identical sibling donors in myelodysplastic syndromes.采用 HLA 全相合同胞供者的异基因造血干细胞移植中,减低强度预处理与传统大剂量预处理用于骨髓增生异常综合征的回顾性比较。
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Optimizing stem cell transplantation in myelodysplastic syndromes: unresolved questions.优化骨髓增生异常综合征中的干细胞移植:未解决的问题。
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Cytogenetics and comorbidity predict outcomes in older myelodysplastic syndrome patients after allogeneic stem cell transplantation using reduced intensity conditioning.细胞遗传学和合并症可预测老年骨髓增生异常综合征患者在接受减低剂量预处理的异基因干细胞移植后的预后。
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Upfront allogeneic stem cell transplantation after reduced-intensity/nonmyeloablative conditioning for patients with myelodysplastic syndrome: a study by the Société Française de Greffe de Moelle et de Thérapie Cellulaire.低强度/非清髓性预处理后 upfront 异基因干细胞移植治疗骨髓增生异常综合征患者:法国骨髓移植和细胞治疗协会的一项研究
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引用本文的文献

1
Getting personal with myelodysplastic syndromes: is now the right time?深入了解骨髓增生异常综合征:现在是合适的时机吗?
Expert Rev Hematol. 2019 Apr;12(4):215-224. doi: 10.1080/17474086.2019.1592673. Epub 2019 Apr 12.

本文引用的文献

1
Myelodysplastic syndromes: toward a risk-adapted treatment approach.骨髓增生异常综合征:朝着风险适应的治疗方法发展。
Expert Rev Hematol. 2013 Oct;6(5):611-24. doi: 10.1586/17474086.2013.840997. Epub 2013 Oct 4.
2
There's risk, and then there's risk: The latest clinical prognostic risk stratification models in myelodysplastic syndromes.有风险,也有风险:骨髓增生异常综合征的最新临床预后风险分层模型。
Curr Hematol Malig Rep. 2013 Dec;8(4):351-60. doi: 10.1007/s11899-013-0172-3.
3
Current therapy of myelodysplastic syndromes.骨髓增生异常综合征的当前治疗。
Blood Rev. 2013 Sep;27(5):243-59. doi: 10.1016/j.blre.2013.07.003. Epub 2013 Jul 27.
4
Role of reduced-intensity conditioning allogeneic hematopoietic stem-cell transplantation in older patients with de novo myelodysplastic syndromes: an international collaborative decision analysis.在新诊断骨髓增生异常综合征的老年患者中,低强度预处理异基因造血干细胞移植的作用:一项国际协作决策分析。
J Clin Oncol. 2013 Jul 20;31(21):2662-70. doi: 10.1200/JCO.2012.46.8652. Epub 2013 Jun 24.
5
Bone marrow transplantation (BMT) in myelodysplastic syndromes: to BMT or not to BMT--that is the question.骨髓增生异常综合征中的骨髓移植:是否进行骨髓移植——这是个问题。
J Clin Oncol. 2013 Jul 20;31(21):2643-4. doi: 10.1200/JCO.2013.48.9146. Epub 2013 Jun 24.
6
Prognostication in myelodysplastic syndromes: beyond the International Prognostic Scoring System (IPSS).骨髓增生异常综合征的预后评估:超越国际预后评分系统(IPSS)
Am J Med. 2013 Apr;126(4):e25. doi: 10.1016/j.amjmed.2012.08.013.
7
The genetic basis of phenotypic heterogeneity in myelodysplastic syndromes.骨髓增生异常综合征表型异质性的遗传基础。
Nat Rev Cancer. 2012 Dec;12(12):849-59. doi: 10.1038/nrc3321.
8
Revised international prognostic scoring system for myelodysplastic syndromes.修订版国际预后积分系统用于骨髓增生异常综合征。
Blood. 2012 Sep 20;120(12):2454-65. doi: 10.1182/blood-2012-03-420489. Epub 2012 Jun 27.
9
Epidemiology of myelodysplastic syndromes.骨髓增生异常综合征的流行病学。
Am J Med. 2012 Jul;125(7 Suppl):S2-5. doi: 10.1016/j.amjmed.2012.04.014.
10
Allogeneic hematopoietic cell transplantation in patients age 60-70 years with de novo high-risk myelodysplastic syndrome or secondary acute myelogenous leukemia: comparison with patients lacking donors who received azacitidine.60-70 岁初治高危骨髓增生异常综合征或继发性急性髓系白血病患者的异基因造血细胞移植:与未找到供体而接受阿扎胞苷治疗的患者比较。
Biol Blood Marrow Transplant. 2012 Sep;18(9):1415-21. doi: 10.1016/j.bbmt.2012.05.003. Epub 2012 May 11.

对于高危骨髓增生异常综合征的老年患者,是否应进行异基因造血干细胞移植?

Should elderly patients with higher-risk myelodysplastic syndromes undergo allogeneic hematopoietic stem cell transplantation?

机构信息

Department of Oncology, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, CRB1 Building, Room 186, Baltimore, MD 21287, USA.

出版信息

Expert Rev Hematol. 2013 Oct;6(5):539-42. doi: 10.1586/17474086.2013.827097. Epub 2013 Oct 4.

DOI:10.1586/17474086.2013.827097
PMID:24093972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4124615/
Abstract

Myelodysplastic syndromes (MDS) include a group of hematopoietic malignancies characterized by dysplastic changes, ineffective hematopoiesis and variable risk of leukemic progression. At diagnosis, 86% of MDS patients are ≥60 years. Azacitidine, the only drug that prolongs life in high-risk (HR)-MDS patients, adds a median of only 9.5 months to life. Allogeneic stem cell transplantation (alloSCT) remains the only potentially curative approach. Despite recent improvements including use of reduced intensity conditioning (RIC) that decrease transplant-related mortality, alloSCT continues to be used rarely in elderly MDS. There is paucity of data regarding outcomes of RIC alloSCT in elderly MDS patients, especially in direct comparison with azanucleosides. In this paper, the authors discuss the recent Markov decision analysis by Koreth et al. in which investigators demonstrated superior survival of patients with HR-MDS aged 60-70 years who underwent RIC alloSCT in comparison with those who were treated with azanucleosides.

摘要

骨髓增生异常综合征(MDS)包括一组造血恶性肿瘤,其特征为发育不良改变、无效造血和白血病进展的不同风险。在诊断时,86%的 MDS 患者年龄≥60 岁。阿扎胞苷是唯一能延长高危(HR)-MDS 患者生命的药物,中位生存期仅延长 9.5 个月。异基因造血干细胞移植(alloSCT)仍然是唯一有潜在治愈作用的方法。尽管最近有所改善,包括使用降低强度的预处理(RIC)降低移植相关死亡率,但 alloSCT 在老年 MDS 患者中仍然很少使用。关于 RIC alloSCT 在老年 MDS 患者中的结果的数据很少,特别是与氮杂核苷的直接比较。在本文中,作者讨论了 Koreth 等人最近的马尔可夫决策分析,该分析表明,60-70 岁 HR-MDS 患者接受 RIC alloSCT 治疗的生存率优于接受氮杂核苷治疗的患者。