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化疗相关性贫血:达贝泊汀 α 的故事。

Chemotherapy-induced anemia: the story of darbepoetin alfa.

机构信息

Respiratory Oncology Unit (Pulmonology), University Hospital Gasthuisberg, Leuven, Belgium.

出版信息

Curr Med Res Opin. 2013 Apr;29(4):325-37. doi: 10.1185/03007995.2013.766593. Epub 2013 Feb 11.

Abstract

BACKGROUND

Prior to the approval of the first erythropoiesis-stimulating agent (ESA) in the early 1990s, red blood cell transfusions were the primary means of treating severe chemotherapy-induced anemia (CIA), with little recourse for those with more mild forms of the condition. The introduction of the ESAs allowed treatment of mild-to-moderate CIA in patients with cancer. It has been a decade since darbepoetin alfa (DA), a second-generation ESA with a longer half-life, became available to patients with CIA.

OBJECTIVE AND METHODS

We present a review of studies on DA in CIA, from its development through to the present day. Medline was searched for randomized clinical trials on DA. Additional trials and meta-analyses on ESAs were incorporated into this review when relevant.

RESULTS

The first publications on DA generally focused on optimal dosing, efficacy and tolerability. In these, it was shown that DA is an effective and well tolerated treatment option to achieve hematopoietic response, regardless of dosing interval. Subsequently, the focus shifted towards meta-analyses on survival data of all ESAs. These reported conflicting results regarding mortality and/or disease progression. However, guidelines for ESA use were updated and, when followed, these make ESAs a well tolerated and effective tool for managing CIA.

CONCLUSIONS

As the past decade has broadened our knowledge on the benefits and risks of CIA management, continued high-quality studies will help to optimize treatment with ESAs in order to maximize quality of life for these patients. The limitation of a literature review of this nature is the complete reliance on previously published research and the availability of these studies using the methodology outlined above.

摘要

背景

在 20 世纪 90 年代初第一种红细胞生成刺激剂(ESA)获得批准之前,红细胞输注是治疗严重化疗诱导性贫血(CIA)的主要手段,对于病情较轻的患者则没有太多的治疗选择。ESA 的引入使得癌症患者的轻至中度 CIA 得到了治疗。自第二个半衰期较长的 ESA 达贝泊汀 α(DA)上市以来,已经过去了十年,用于 CIA 的治疗。

目的和方法

我们回顾了 CIA 中 DA 的研究,从开发到现在。在 Medline 上搜索了关于 DA 的随机临床试验。当相关时,将有关 ESA 的其他试验和荟萃分析纳入了本综述。

结果

关于 DA 的第一批出版物通常侧重于最佳剂量、疗效和耐受性。在这些研究中,DA 是一种有效的且耐受性良好的治疗选择,可以实现血液学反应,无论剂量间隔如何。随后,重点转向了关于所有 ESA 的生存数据的荟萃分析。这些报告的死亡率和/或疾病进展结果相互矛盾。然而,ESA 使用指南进行了更新,并且遵循这些指南使 ESA 成为管理 CIA 的一种耐受性良好且有效的工具。

结论

随着过去十年我们对 CIA 管理的益处和风险的了解不断加深,持续进行高质量的研究将有助于优化 ESA 的治疗,从而最大程度地提高这些患者的生活质量。这种性质的文献综述的局限性在于完全依赖以前发表的研究,以及使用上述方法进行这些研究的可用性。

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