• 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

β-促红细胞生成素每周一次:化疗所致贫血患者疗效与安全性综述

Epoetin beta once weekly: review of its efficacy and safety in patients with chemotherapy-induced anemia.

作者信息

Spaëth Dominique

机构信息

Oncologie Médicale, Centre d'Oncologie de Gentilly, 2 rue Marie Marvingt, 54100 Nancy, France.

出版信息

Expert Rev Anticancer Ther. 2008 Jun;8(6):875-85. doi: 10.1586/14737140.8.6.875.

DOI:10.1586/14737140.8.6.875
PMID:18533797
Abstract

Epoetin beta effectively increases hemoglobin levels, reduces the need for transfusions and improves the quality of life in patients with symptomatic chemotherapy-induced anemia with a range of solid tumors and lymphoid malignancies. Recent evidence-based guidelines recommend the once weekly administration of epoetin beta. This once-weekly regimen is generally well tolerated, and studies to date have reported that epoetin beta has a neutral effect on survival of patients with cancer. The once-weekly administration regimen is convenient for the physician and patient alike. Methods to further optimize this treatment are discussed.

摘要

β-促红细胞生成素能有效提高血红蛋白水平,减少输血需求,并改善患有一系列实体瘤和淋巴恶性肿瘤的有症状化疗所致贫血患者的生活质量。最近基于证据的指南推荐每周一次使用β-促红细胞生成素。这种每周一次的治疗方案通常耐受性良好,且迄今为止的研究报告称β-促红细胞生成素对癌症患者的生存具有中性影响。每周一次的给药方案对医生和患者而言都很方便。文中还讨论了进一步优化这种治疗的方法。

相似文献

1
Epoetin beta once weekly: review of its efficacy and safety in patients with chemotherapy-induced anemia.β-促红细胞生成素每周一次:化疗所致贫血患者疗效与安全性综述
Expert Rev Anticancer Ther. 2008 Jun;8(6):875-85. doi: 10.1586/14737140.8.6.875.
2
Antianemic effect of once weekly regimen of epoetin alfa 40,000 units in anemic cancer patients receiving chemotherapy.对于接受化疗的贫血癌症患者,每周一次注射40,000单位促红细胞生成素α的抗贫血效果。
J Med Assoc Thai. 2007 Jun;90(6):1082-8.
3
Once-weekly epoetin beta therapy in patients with solid tumours and chemotherapy-induced anaemia: a randomized, double-blind, dose-finding study.实体瘤和化疗所致贫血患者的每周一次促红细胞生成素β治疗:一项随机、双盲、剂量探索性研究。
Eur J Cancer Care (Engl). 2008 Nov;17(6):619-23. doi: 10.1111/j.1365-2354.2007.00892.x. Epub 2008 Aug 13.
4
Epoetin Beta once-weekly therapy in anemic patients with solid tumors and non-myeloid hematological malignancies receiving chemotherapy.对接受化疗的实体瘤和非髓系血液系统恶性肿瘤贫血患者进行促红细胞生成素β每周一次的治疗。
Oncology. 2008;74(1-2):112-8. doi: 10.1159/000139139. Epub 2008 Jun 12.
5
[Efficacy of weekly epoetin Beta in the treatment of chemotherapy-induced anemia in solid tumors].[每周一次使用β-促红细胞生成素治疗实体瘤化疗所致贫血的疗效]
Therapie. 2009 Jan-Feb;64(1):17-25. doi: 10.2515/therapie/2009002. Epub 2009 May 26.
6
Epoetin beta therapy in patients with solid tumours.β-促红细胞生成素治疗实体瘤患者。
Crit Rev Oncol Hematol. 2006 Apr;58(1):46-52. doi: 10.1016/j.critrevonc.2005.08.010. Epub 2005 Oct 5.
7
Treatment of cancer-related anemia with epoetin alfa: a review.促红细胞生成素α治疗癌症相关性贫血的综述
Cancer Treat Rev. 2004 Oct;30(6):563-75. doi: 10.1016/j.ctrv.2004.04.005.
8
Efficacy of once-weekly intravenous administration of epoetin-beta as a maintenance treatment for anemia in Japanese hemodialysis patients: a multicenter, open-label clinical study.日本血液透析患者中每周一次静脉注射依泊汀β作为贫血维持治疗的疗效:一项多中心、开放标签的临床研究。
Ther Apher Dial. 2008 Dec;12(6):469-74. doi: 10.1111/j.1744-9987.2008.00637.x.
9
Once-weekly epoetin beta (30,000 IU) in anemic patients with lung cancer receiving chemotherapy.接受化疗的肺癌贫血患者每周一次使用促红细胞生成素β(30,000国际单位)。
Lung Cancer. 2007 Jan;55(1):89-94. doi: 10.1016/j.lungcan.2006.09.020. Epub 2006 Nov 3.
10
Erythropoiesis-stimulating agents: favorable safety profile when used as indicated.促红细胞生成素:按指示使用时安全性良好。
Strahlenther Onkol. 2008 Mar;184(3):121-36. doi: 10.1007/s00066-008-1841-3.

引用本文的文献

1
Recombinant human epoetin beta in the treatment of chemotherapy-related anemia.重组人促红素β在化疗相关性贫血治疗中的应用。
Ther Clin Risk Manag. 2009 Feb;5(1):261-70. doi: 10.2147/tcrm.s3320. Epub 2009 Mar 26.