Suppr超能文献

促红细胞生成素和达比加群酯在癌症患者中的应用:2007年美国血液学会/美国临床肿瘤学会临床实践指南更新

Use of epoetin and darbepoetin in patients with cancer: 2007 American Society of Hematology/American Society of Clinical Oncology clinical practice guideline update.

作者信息

Rizzo J Douglas, Somerfield Mark R, Hagerty Karen L, Seidenfeld Jerome, Bohlius Julia, Bennett Charles L, Cella David F, Djulbegovic Benjamin, Goode Matthew J, Jakubowski Ann A, Rarick Mark U, Regan David H, Lichtin Alan E

机构信息

Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Blood. 2008 Jan 1;111(1):25-41. doi: 10.1182/blood-2007-08-109488. Epub 2007 Oct 22.

Abstract

PURPOSE

To update the American Society of Clinical Oncology/American Society of Hematology (ASCO/ASH) recommendations for the use of epoetin. The guideline was expanded to address use of darbepoetin and thromboembolic risk associated with these agents.

METHOD

An Update Committee ("Committee") reviewed and analyzed data published since 2002 through July 2007. MEDLINE and the Cochrane Collaboration Library databases were searched.

RECOMMENDATIONS

For patients with chemotherapy-associated anemia, the Committee continues to recommend initiating an erythropoiesis-stimulating agent (ESA) as hemoglobin (Hb) approaches, or falls below, 10 g/dL, to increase Hb and decrease transfusions. ESA treatment continues to be recommended for patients with low-risk myelodysplasia for similar reasons. There is no evidence showing increased survival as a result of ESA treatment. Conclusive evidence is lacking that, absent clinical circumstances necessitating earlier treatment, initiating ESAs at Hb levels greater than 10 g/dL either spares more patients from transfusion or substantially improves their quality of life. Starting doses and dose modifications based on response or lack thereof should follow the package insert. Continuing ESAs beyond 6 to 8 weeks in the absence of response, assuming appropriate dose increase has been attempted in nonresponders as per US Food and Drug Administration-approved label, does not seem to be beneficial, and ESA therapy should be discontinued. The Committee recommends monitoring iron stores and supplementing iron intake for ESA-treated patients. ESAs should be used cautiously with chemotherapy, or in clinical states, associated with elevated risk for thromo-embolic complications. The Committee also cautions against ESA use for patients with cancer who are not receiving chemotherapy, since recent trials report increased thromboembolic risks and decreased survival under these circumstances.

摘要

目的

更新美国临床肿瘤学会/美国血液学会(ASCO/ASH)关于促红细胞生成素使用的建议。该指南已扩展,以涵盖达贝泊汀的使用以及与这些药物相关的血栓栓塞风险。

方法

一个更新委员会(“委员会”)对2002年至2007年7月期间发表的数据进行了审查和分析。检索了MEDLINE和Cochrane协作图书馆数据库。

建议

对于化疗相关性贫血患者,委员会继续建议在血红蛋白(Hb)接近或降至10 g/dL以下时开始使用促红细胞生成素刺激剂(ESA),以提高Hb水平并减少输血。出于类似原因,对于低危骨髓增生异常综合征患者,仍建议使用ESA治疗。没有证据表明ESA治疗能提高生存率。缺乏确凿证据表明,在没有需要更早治疗的临床情况时,在Hb水平高于10 g/dL时开始使用ESA能使更多患者避免输血或显著改善其生活质量。起始剂量和根据反应与否进行的剂量调整应遵循药品说明书。在无反应的情况下,ESA治疗超过6至8周(假设已按照美国食品药品监督管理局批准的标签对无反应者尝试了适当的剂量增加)似乎并无益处,应停止ESA治疗。委员会建议对接受ESA治疗的患者监测铁储备并补充铁摄入。ESA与化疗联合使用或在血栓栓塞并发症风险升高的临床状态下应谨慎使用。委员会还告诫不要对未接受化疗的癌症患者使用ESA,因为最近的试验报告在这些情况下血栓栓塞风险增加且生存率降低。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验