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重组人促红细胞生成素用于癌症相关性贫血。临床证据综述。

Recombinant human erythropoietin in cancer-related anemia. Review of clinical evidence.

作者信息

Crawford Jeffrey

机构信息

Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Oncology (Williston Park). 2002 Sep;16(9 Suppl 10):41-53.

Abstract

The clinical development of recombinant human erythropoietin (rHuEPO) has had a remarkable impact on the clinical practice of oncology. A decade ago, randomized, placebo-controlled trials in anemic cancer patients demonstrated that rHuEPO resulted in an improvement in hemoglobin and hematocrit, a reduction in transfusion requirements, and improvement in quality-of-life (QOL) end points. Based on these trials, recombinant erythropoietin was approved for the treatment of anemia in patients with nonmyeloid malignancies in whom the anemia was caused by the effect of chemotherapy. The clinical indication was to decrease the needfor transfusion in patients for whom anemia was not due to other reversible causes. Despite this broad indication, the incorporation of rHuEPO in clinical practice was limited because of a variety of factors, including physician perception that mild-to-moderate anemia in the cancer patient was generally asymptomatic and did not warrant intervention. Subsequently, three large open-label, prospective trials of recombinant erythropoietin were performed in the community setting in anemic cancer chemotherapy patients. All three trials replicated the results of the original randomized study, but with a much larger database of more than 7,000 patients. Importantly, these trials were able to define the major impact of hemoglobin level on quality of life. Patients on these trials who improved their hemoglobin > 2 g/dL or achieved a hemoglobin > or = 12 g/ dL had the greatest improvement in symptoms of energy, activities of daily living, and overall quality of life. Furthermore, a once-per-week dosing schedule was found to be comparable to three-times-weekly administration of rHuEPO. A European randomized, placebo-controlled trial confirmed these QOL results, and a meta-analysis of other randomized clinical trials firmly supports the role of erythropoietin therapy in improving hemoglobin levels and reducing transfusion requirements. Based on this aggregate of data, the use of erythropoietin in the treatment of mild-to-moderate anemia has become a standard of care. These studies have also expanded our understanding of the problem of fatigue and the study of interventions that can improve quality of life for cancer patients.

摘要

重组人促红细胞生成素(rHuEPO)的临床开发对肿瘤学临床实践产生了显著影响。十年前,针对贫血癌症患者的随机、安慰剂对照试验表明,rHuEPO可使血红蛋白和血细胞比容得到改善,输血需求减少,生活质量(QOL)终点指标得到改善。基于这些试验,重组促红细胞生成素被批准用于治疗非髓系恶性肿瘤患者的贫血,这些患者的贫血是由化疗作用引起的。临床适应证是减少非其他可逆性病因所致贫血患者的输血需求。尽管有这一广泛适应证,但由于多种因素,rHuEPO在临床实践中的应用有限,包括医生认为癌症患者的轻至中度贫血通常无症状,无需干预。随后,在社区环境中对贫血癌症化疗患者进行了三项大型开放标签、前瞻性重组促红细胞生成素试验。所有三项试验都重复了最初随机研究的结果,但数据库规模更大,有超过7000名患者。重要的是,这些试验能够确定血红蛋白水平对生活质量的主要影响。在这些试验中,血红蛋白改善>2 g/dL或血红蛋白达到>或=12 g/dL的患者在精力、日常生活活动和总体生活质量症状方面改善最大。此外,发现每周一次的给药方案与每周三次给予rHuEPO相当。一项欧洲随机、安慰剂对照试验证实了这些生活质量结果,对其他随机临床试验的荟萃分析有力地支持了促红细胞生成素治疗在提高血红蛋白水平和减少输血需求方面的作用。基于这些汇总数据,促红细胞生成素用于治疗轻至中度贫血已成为一种标准治疗方法。这些研究还扩展了我们对疲劳问题的理解以及对可改善癌症患者生活质量干预措施的研究。

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