Lund Anton, Lundby Carsten, Olsen Niels V
Department of Neuroscience and Pharmacology, The Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Eur J Clin Invest. 2014 Dec;44(12):1230-8. doi: 10.1111/eci.12357. Epub 2014 Nov 9.
The discovery of potential anti-apoptotic and cytoprotective effects of recombinant human erythropoietin (rHuEPO) has led to clinical trials investigating the use of high-dose, short-term rHuEPO therapy for tissue protection in conditions such as stroke and myocardial infarction. Experimental studies have been favourable, but the clinical efficacy has yet to be validated.
We have reviewed clinical studies regarding the use of high-dose, short-term rHuEPO therapy for tissue protection in humans with the purpose to detail the safety and efficacy of rHuEPO for this indication. A systematic literature search was performed using the PubMed/MEDLINE database for randomized, placebo-controlled clinical trials.
Twenty-six randomized controlled trials that enrolled 3176 patients were included. The majority of trials (20 trials including 2724 patients) reported no effect of rHuEPO therapy on measures of tissue protection. Five trials including 1025 patients reported safety concerns in the form of increased mortality or adverse event rates. No studies reported reduced mortality.
Evidence is sparse to support a tissue-protective benefit of rHuEPO in humans. Moreover, a number of studies indicate that short-term administration of high-dose rHuEPO is associated with an increased risk of mortality and serious adverse events. Further work is needed to elucidate the mechanisms of toxicity of rHuEPO in humans.
重组人促红细胞生成素(rHuEPO)潜在的抗凋亡和细胞保护作用的发现,引发了关于在中风和心肌梗死等病症中使用高剂量、短期rHuEPO疗法进行组织保护的临床试验。实验研究结果良好,但临床疗效尚未得到验证。
我们回顾了关于使用高剂量、短期rHuEPO疗法对人类进行组织保护的临床研究,目的是详细阐述rHuEPO用于该适应症的安全性和有效性。使用PubMed/MEDLINE数据库进行系统的文献检索,以查找随机、安慰剂对照的临床试验。
纳入了26项随机对照试验,共3176例患者。大多数试验(20项试验,包括2724例患者)报告rHuEPO疗法对组织保护指标无影响。5项试验(包括1025例患者)报告了以死亡率增加或不良事件发生率增加形式出现的安全问题。没有研究报告死亡率降低。
支持rHuEPO对人类具有组织保护益处的证据不足。此外,多项研究表明,短期给予高剂量rHuEPO与死亡率增加和严重不良事件风险增加相关。需要进一步开展工作以阐明rHuEPO在人类中的毒性机制。