Markham A, Bryson H M
Adis International Limited, Auckland, New Zealand.
Drugs. 1995 Feb;49(2):232-54. doi: 10.2165/00003495-199549020-00008.
Epoetin alfa is a recombinant form of the principal hormone responsible for erythrogenesis, erythropoietin. Already an established treatment for anaemia associated with renal failure, epoetin alfa may also be used to correct anaemia in other patient groups. The drug increases the capacity for autologous blood donation in patients scheduled to undergo surgery and attenuates the decrease in haematocrit often seen in untreated autologous donors. However, transfusion requirements did not significantly decrease in many trials. Epoetin alfa also accelerates red blood cell recovery after allogeneic--but not autologous--bone marrow transplant. Limited data in patients with adult rheumatoid arthritis suggest that while epoetin alfa increases haematocrit/haemoglobin levels, overall clinical rheumatological status may not improve. However, the drug did improve quality of life in a small cohort of children with juvenile rheumatoid arthritis in addition to correcting anaemia. Response rates to treatment with epoetin alfa in patients with anaemia associated with cancer range between 32 and 85%. Anaemia associated with cancer chemotherapy also responds well to treatment with the drug as does anaemia associated with zidovudine therapy in patients with acquired immune deficiency syndrome (AIDS). Studies evaluating the use of epoetin alfa as treatment for anaemia of prematurity have used different methodologies and dosages, making overall analysis difficult. Nevertheless, it appears that high dosages are necessary for response. Results from 1 study suggest that treatment with epoetin alfa appears to be more costly than transfusional support in this application; the relevance of this finding is questionable, however, given that the aim of treatment with epoetin alfa is elimination of transfusion requirements. The incidence of many adverse events associated with epoetin alfa treatment in patients with renal failure (hypertension, seizures and thromboembolic events) has been minimal in patients without renal failure. Adverse events occurred at a similar rate in placebo and epoetin alfa recipients in placebo-controlled trials evaluating the use of the drug as treatment for anaemia in patients with cancer receiving chemotherapy or patients with AIDS receiving zidovudine. In summary, epoetin alfa is an effective alternative to blood transfusion, reducing anaemia and producing consequent improvements in quality of life in many nonrenal applications. It was more effective than placebo in a number of double-blind trials and may be particularly useful as treatment for anaemia associated with other drugs such as cisplatin and zidovudine.
促红细胞生成素α是负责红细胞生成的主要激素促红细胞生成素的重组形式。促红细胞生成素α已成为治疗与肾衰竭相关贫血的既定疗法,也可用于纠正其他患者群体的贫血。该药物可提高计划接受手术患者的自体献血能力,并减轻未治疗的自体献血者中常见的血细胞比容下降。然而,在许多试验中输血需求并未显著降低。促红细胞生成素α还可加速异基因(而非自体)骨髓移植后红细胞的恢复。成年类风湿关节炎患者的有限数据表明,虽然促红细胞生成素α可提高血细胞比容/血红蛋白水平,但整体临床风湿病状况可能并未改善。然而,该药物除了纠正贫血外,还确实改善了一小群幼年类风湿关节炎患儿的生活质量。与癌症相关贫血患者使用促红细胞生成素α治疗的缓解率在32%至85%之间。与癌症化疗相关的贫血对该药物治疗反应良好,获得性免疫缺陷综合征(AIDS)患者中与齐多夫定治疗相关的贫血也是如此。评估促红细胞生成素α用于治疗早产儿贫血的研究采用了不同的方法和剂量,使得全面分析变得困难。然而,似乎需要高剂量才能产生反应。一项研究的结果表明,在这种应用中,促红细胞生成素α治疗似乎比输血支持成本更高;然而,鉴于促红细胞生成素α治疗的目的是消除输血需求,这一发现的相关性值得怀疑。在没有肾衰竭的患者中,与促红细胞生成素α治疗相关的许多不良事件(高血压、癫痫发作和血栓栓塞事件)的发生率极低。在评估该药物用于接受化疗的癌症患者或接受齐多夫定的AIDS患者贫血治疗的安慰剂对照试验中,安慰剂和促红细胞生成素α接受者的不良事件发生率相似。总之,促红细胞生成素α是输血的有效替代方法,可减少贫血并在许多非肾脏应用中相应改善生活质量。在一些双盲试验中,它比安慰剂更有效,可能特别适用于治疗与顺铂和齐多夫定等其他药物相关的贫血。