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American Society of Hematology/American Society of Clinical Oncology clinical practice guideline update on the use of epoetin and darbepoetin in adult patients with cancer

机译:美国血液学会/美国临床肿瘤学会临床实践指南更新关于成年癌症患者使用依泊汀和达比泊汀的情况

摘要

Purpose: To update American Society of Hematology/American Society of Clinical Oncology recommendations for use of erythropoiesis-stimulating agents (ESAs) in patients with cancer. Methods: An Update Committee reviewed data published between January 2007 and January 2010. MEDLINE and the Cochrane Library were searched. Results: The literature search yielded one new individual patient data analysis and four literature-based meta-analyses, two systematic reviews, and 13 publications reporting new results from randomized controlled trials not included in prior or new reviews. Recommendations: For patients undergoing myelosuppressive chemotherapy who have a hemoglobin (Hb) level less than 10 g/dL, the Update Committee recommends that clinicians discuss potential harms (eg, thromboembolism, shorter survival) and benefits (eg, decreased transfusions) of ESAs and compare these with potential harms (eg, serious infections, immune-mediated adverse reactions) and benefits (eg, rapid Hb improvement) of RBC transfusions. Individual preferences for assumed risk should contribute to shared decisions on managing chemotherapy-induced anemia. The Committee cautions against ESA use under other circumstances. If used, ESAs should be administered at the lowest dose possible and should increase Hb to the lowest concentration possible to avoid transfusions. Available evidence does not identify Hb levels 10 g/dL either as thresholds for initiating treatment or as targets for ESA therapy. Starting doses and dose modifications after response or nonresponse should follow US Food and Drug Administration-approved labeling. ESAs should be discontinued after 6 to 8 weeks in nonresponders. ESAs should be avoided in patients with cancer not receiving concurrent chemotherapy, except for those with lower risk myelodysplastic syndromes. Caution should be exercised when using ESAs with chemotherapeutic agents in diseases associated with increased risk of thromboembolic complications. Table 1 lists detailed recommendations.
机译:目的:更新美国血液病学会/美国临床肿瘤学会关于在癌症患者中使用促红细胞生成素(ESA)的建议。方法:更新委员会审查了2007年1月至2010年1月之间发布的数据。检索了MEDLINE和Cochrane库。结果:文献检索产生了一项新的个人患者数据分析和四项基于文献的荟萃分析,两项系统评价以及13篇文献报道了先前或新评价中未包括的随机对照试验的新结果。建议:对于接受骨髓抑制化学疗法的血红蛋白(Hb)水平低于10 g / dL的患者,更新委员会建议临床医生讨论ESA的潜在危害(例如血栓栓塞,生存期缩短)和获益(例如输血减少)。将其与RBC输血的潜在危害(例如,严重感染,免疫介导的不良反应)和益处(例如,快速的血红蛋白改善)进行比较。个体对假定风险的偏好应有助于共同决定治疗化疗引起的贫血。委员会告诫不要在其他情况下使用ESA。如果使用ESA,应以尽可能低的剂量给药,并应将Hb增加到尽可能低的浓度,以避免输血。现有证据不能将Hb水平10 g / dL确定为开始治疗的阈值或ESA治疗的目标。反应或无反应后的起始剂量和剂量调整应遵循美国食品药品监督管理局批准的标签。对于无反应者,应在6至8周后停用ESA。对于患有低风险骨髓增生异常综合症的患者,应避免在未同时接受化疗的癌症患者中使用ESA。在与血栓栓塞性并发症风险增加相关的疾病中使用ESA和化学治疗剂时应谨慎。表1列出了详细的建议。

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