• 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

Prolonged administration of erythropoietin increases erythroid response rate in myelodysplastic syndromes: a phase II trial in 281 patients.

作者信息

Terpos Evangelos, Mougiou Athina, Kouraklis Alexandra, Chatzivassili Aria, Michalis Evridiki, Giannakoulas Nicholas, Manioudaki Eleni, Lazaridou Anna, Bakaloudi Vassiliki, Protopappa Maria, Liapi Dimitra, Grouzi Elisavet, Parharidou Agapi, Symeonidis Argyris, Kokkini Garoufalia, Laoutaris Nikolaos P, Vaipoulos George, Anagnostopoulos Nikolaos I, Christakis John I, Meletis John, Bourantas Konstantinos L, Zoumbos Nicholas C, Yataganas Xenophon, Viniou Nora-Athina

机构信息

Department of Haematology, Faculty of Medicine, Imperial College of Science, Technology and Medicine, Hammersmith Hospital, London, UK.

出版信息

Br J Haematol. 2002 Jul;118(1):174-80. doi: 10.1046/j.1365-2141.2002.03583.x.

DOI:10.1046/j.1365-2141.2002.03583.x
PMID:12100145
Abstract

Treatment with recombinant human erythropoietin (rHuEpo) improves anaemia in approximately 20% of patients with myelodysplastic syndromes (MDS). We investigated the potential advantage of a prolonged administration of rHuEpo to achieve higher erythroid response rates (RR) in 281 MDS patients: 118 with refractory anaemia (RA), 77 with refractory anaemia and ringed sideroblasts (RARS), 59 with refractory anaemia with excess of blasts and blast count < 10% (RAEB-I), and 27 with RAEB and blast count between 11-20% (RAEB-II). rHuEpo was given subcutaneously at a dose of 150 U/kg thrice weekly, for a minimum of 26 weeks. Response to treatment was evaluated after 12 and 26 weeks of therapy. The overall RR was 45.1%; the RR for RA, RARS, RAEB-I and RAEB-II were 48.3%, 58.4%, 33.8% and 13% respectively. A significant increase in RR was observed at week 26 in RA, RARS and RAEB-I patients, as the response probability increased with treatment duration. The RR was higher in the good cytogenetic prognostic group and serum Epo level of > 150 U/l at baseline predicted for non-response. The median duration of response was 68 weeks and the overall risk of leukaemic transformation was 21.7%. These results suggest that prolonged administration of rHuEpo produces high and long-lasting erythroid RR in MDS patients with low blast counts, particularly in those with pretreatment serum Epo levels of < 150 U/l and good cytogenetic prognosis.

摘要

相似文献

1
Prolonged administration of erythropoietin increases erythroid response rate in myelodysplastic syndromes: a phase II trial in 281 patients.
Br J Haematol. 2002 Jul;118(1):174-80. doi: 10.1046/j.1365-2141.2002.03583.x.
2
Investigation for the presence of anti-erythropoietin antibodies in patients with myelodysplastic syndromes.骨髓增生异常综合征患者抗促红细胞生成素抗体存在情况的调查。
Eur J Haematol. 2001 Jan;66(1):31-6. doi: 10.1034/j.1600-0609.2001.00336.x.
3
Treatment of anemia in low risk myelodysplastic syndromes with granulocyte-macrophage colony-stimulating factor plus recombinant human erythropoietin.粒细胞-巨噬细胞集落刺激因子联合重组人促红细胞生成素治疗低危骨髓增生异常综合征贫血
Leukemia. 1999 Jul;13(7):1009-12. doi: 10.1038/sj.leu.2401442.
4
Treatment of anaemia in myelodysplastic syndromes with prolonged administration of recombinant human granulocyte colony-stimulating factor and erythropoietin.重组人粒细胞集落刺激因子和促红细胞生成素长期给药治疗骨髓增生异常综合征中的贫血
Br J Haematol. 2000 May;109(2):367-75. doi: 10.1046/j.1365-2141.2000.02016.x.
5
High doses of intravenous recombinant erythropoietin for the treatment of anaemia in myelodysplastic syndrome.大剂量静脉注射重组促红细胞生成素治疗骨髓增生异常综合征贫血
Br J Haematol. 1993 Jun;84(2):232-7. doi: 10.1111/j.1365-2141.1993.tb03057.x.
6
Recombinant human erythropoietin (rHuEPO) for treatment of myelodysplastic syndrome.重组人促红细胞生成素(rHuEPO)用于治疗骨髓增生异常综合征。
Stem Cells. 1993 Jan;11(1):49-55. doi: 10.1002/stem.5530110109.
7
Serum erythropoietin (EPO) levels correlate with survival and independently predict response to EPO treatment in patients with myelodysplastic syndromes.血清促红细胞生成素(EPO)水平与骨髓增生异常综合征患者的生存率相关,并能独立预测对EPO治疗的反应。
Eur J Haematol. 2002 Mar;68(3):180-5. doi: 10.1034/j.1600-0609.2002.01530.x.
8
Refractory cytopenia with multilineage dysplasia: further characterization of an 'unclassifiable' myelodysplastic syndrome.伴有多系发育异常的难治性血细胞减少症:一种“无法分类”的骨髓增生异常综合征的进一步特征描述
Leukemia. 1996 Jan;10(1):20-6.
9
Long-term follow-up of myelodysplastic syndrome patients with moderate/severe anaemia receiving human recombinant erythropoietin + 13-cis-retinoic acid and dihydroxylated vitamin D3: independent positive impact of erythroid response on survival.中危/高危骨髓增生异常综合征患者接受人重组红细胞生成素+13-顺式维甲酸和二羟维生素 D3 治疗的长期随访:红细胞反应对生存的独立正向影响。
Br J Haematol. 2012 Jul;158(1):99-107. doi: 10.1111/j.1365-2141.2012.09125.x. Epub 2012 May 10.
10
Recombinant human erythropoietin in patients with myelodysplastic syndromes.重组人促红细胞生成素用于骨髓增生异常综合征患者
Leukemia. 1991 May;5(5):432-6.

引用本文的文献

1
[Efficacy and safety analysis of hypoxia-inducible factor prolyl hydroxylase inhibitors for anemia in low-risk myelodysplastic syndromes patients].低危骨髓增生异常综合征患者贫血应用缺氧诱导因子脯氨酰羟化酶抑制剂的疗效与安全性分析
Zhonghua Xue Ye Xue Za Zhi. 2024 Mar 14;45(3):290-293. doi: 10.3760/cma.j.cn121090-20230825-00089.
2
Long-Term Efficacy of Erythropoiesis-Stimulating Agents in Patients with Low-Risk or Intermediate-1-Risk Myelodysplastic Syndrome: Multicenter Real-Life Data.低危或中危-1 风险骨髓增生异常综合征患者使用红细胞生成刺激剂的长期疗效:多中心真实世界数据。
Turk J Haematol. 2023 May 29;40(2):92-100. doi: 10.4274/tjh.galenos.2023.2022.0437. Epub 2023 Feb 17.
3
The Clinical Efficacy of Epoetin Alfa and Darbepoetin Alfa in Patients with Low-Risk or Intermediate-1-Risk Myelodysplastic Syndrome: Retrospective Multi-center Real-Life Study.
阿法依泊汀和阿法达贝泊汀治疗低危或中危-1骨髓增生异常综合征患者的临床疗效:回顾性多中心真实世界研究
Indian J Hematol Blood Transfus. 2022 Apr;38(2):299-308. doi: 10.1007/s12288-021-01458-1. Epub 2021 Jun 26.
4
Response Assessment to Erythropoietin-Zeta (Epo-Alpha Biosimilar) Therapy in Low-Risk Myelodysplastic Syndromes.低危骨髓增生异常综合征中促红细胞生成素ζ(促红细胞生成素α生物类似药)治疗的疗效评估
J Clin Med. 2022 Mar 17;11(6):1665. doi: 10.3390/jcm11061665.
5
Erythropoiesis-stimulating agents and cardiovascular events in patients with myelodysplastic syndrome and multiple myeloma.红细胞生成刺激剂与骨髓增生异常综合征和多发性骨髓瘤患者的心血管事件
Clin Epidemiol. 2018 Sep 28;10:1371-1380. doi: 10.2147/CLEP.S172306. eCollection 2018.
6
A phase 3 randomized, placebo-controlled study assessing the efficacy and safety of epoetin-α in anemic patients with low-risk MDS.一项评估低危 MDS 贫血患者使用促红细胞生成素-α的疗效和安全性的 3 期随机、安慰剂对照研究。
Leukemia. 2018 Dec;32(12):2648-2658. doi: 10.1038/s41375-018-0118-9. Epub 2018 Mar 30.
7
A phase 3 randomized placebo-controlled trial of darbepoetin alfa in patients with anemia and lower-risk myelodysplastic syndromes.一项关于聚乙二醇化促红细胞生成素α治疗贫血合并低危骨髓增生异常综合征患者的3期随机安慰剂对照试验。
Leukemia. 2017 Sep;31(9):1944-1950. doi: 10.1038/leu.2017.192. Epub 2017 Jun 19.
8
Exploring Erythropoietin and G-CSF Combination Therapy in Chronic Stroke Patients.探索促红细胞生成素与粒细胞集落刺激因子联合疗法对慢性中风患者的疗效
Int J Mol Sci. 2016 Mar 30;17(4):463. doi: 10.3390/ijms17040463.
9
Variations in erythropoiesis-stimulating agent administration in transfusion-dependent myelodysplastic syndromes impact response.输血依赖型骨髓增生异常综合征中促红细胞生成素刺激剂给药方式的差异会影响疗效。
Leuk Res. 2015 Jun;39(6):586-91. doi: 10.1016/j.leukres.2015.03.013. Epub 2015 Mar 28.
10
Resuscitating a dying marrow: the role of hematopoietic growth factors.挽救濒死的骨髓:造血生长因子的作用
Curr Hematol Malig Rep. 2014 Dec;9(4):412-20. doi: 10.1007/s11899-014-0236-z.