Dunn C J, Wagstaff A J
Adis International Limited, Auckland, New Zealand.
Drugs Aging. 1995 Aug;7(2):131-56. doi: 10.2165/00002512-199507020-00007.
Epoetin alfa is a recombinant form of erythropoietin, a glycoprotein hormone which stimulates red blood cell production by stimulating the activity of erythroid progenitor cells. This review discusses the use of the drug in the management of anaemia in diseases often associated with advancing age [renal failure, cancer, rheumatoid arthritis (RA) and other chronic diseases, and the myelodysplastic syndromes (MDS)] and in surgical patients. Intravenous and subcutaneous therapy with epoetin alfa raises haematocrit and haemoglobin levels, and reduces transfusion requirements, in anaemic patients with end-stage renal failure undergoing haemodialysis or peritoneal dialysis. The drug is also effective in the correction of anaemia in patients with chronic renal failure not yet requiring dialysis and does not appear to affect renal haemodynamics adversely or to precipitate the onset of end-stage renal failure. Response rates of 32 to 82% with epoetin alfa therapy have been reported in patients with anaemia associated with cancer or cytotoxic chemotherapy. Limited data in patients with anaemia associated with RA show correction of anaemia after epoetin alfa treatment. Response rates to the drug of 0 to 56% have been noted in patients with MDS. Epoetin alfa also reduces anaemia, increases the capacity for autologous blood donation and reduces the need for allogeneic blood transfusion in patients scheduled to undergo surgery. Hypertension occurs in 30 to 35% of patients with end-stage renal failure who receive epoetin alfa, but this can be managed successfully with correction of fluid status and antihypertensive medication where necessary, and is minimised by avoiding rapid increases in haematocrit. Although vascular access thrombosis has not been conclusively linked to therapy with the drug, increased heparinisation may be required when it is administered to patients on haemodialysis. Epoetin alfa does not appear to exert any direct cerebrovascular adverse effects. Thus, epoetin alfa is a well established and effective therapy for the management of anaemia associated with renal failure. It also improves haematocrit and quality of life in patients with anaemia associated with cancer or chemotherapy. Epoetin alfa increases the capacity for blood donation and reduces the decrease in haematocrit seen in patients donating autologous blood prior to surgery. It also reduces, but may not eliminate, the need for allogeneic blood transfusion.(ABSTRACT TRUNCATED AT 400 WORDS)
促红细胞生成素α是促红细胞生成素的重组形式,促红细胞生成素是一种糖蛋白激素,通过刺激红系祖细胞的活性来刺激红细胞生成。本综述讨论了该药物在治疗常与年龄增长相关的疾病(肾衰竭、癌症、类风湿关节炎(RA)和其他慢性病以及骨髓增生异常综合征(MDS))所致贫血中的应用,以及在外科手术患者中的应用。对于接受血液透析或腹膜透析的终末期肾衰竭贫血患者,静脉和皮下注射促红细胞生成素α可提高血细胞比容和血红蛋白水平,并减少输血需求。该药物对尚未需要透析的慢性肾衰竭患者纠正贫血也有效,且似乎不会对肾脏血流动力学产生不利影响,也不会促使终末期肾衰竭的发生。据报道,促红细胞生成素α治疗癌症或细胞毒性化疗相关贫血患者的有效率为32%至82%。关于RA相关贫血患者的数据有限,显示促红细胞生成素α治疗后贫血得到纠正。MDS患者对该药物的有效率为0%至56%。促红细胞生成素α还可减轻手术患者的贫血,增加自体献血能力,减少异体输血需求。接受促红细胞生成素α治疗的终末期肾衰竭患者中,30%至35%会出现高血压,但必要时可通过纠正液体状态和使用抗高血压药物成功控制,且通过避免血细胞比容快速升高可将其降至最低。虽然血管通路血栓形成与该药物治疗尚未有确凿关联,但在给血液透析患者使用时可能需要增加肝素化。促红细胞生成素α似乎不会产生任何直接的脑血管不良反应。因此,促红细胞生成素α是治疗肾衰竭相关贫血的一种成熟且有效的疗法。它还可改善癌症或化疗相关贫血患者的血细胞比容和生活质量。促红细胞生成素α可增加献血能力,减少手术前自体献血患者血细胞比容的下降。它还可减少但可能无法消除异体输血的需求。(摘要截选至400字)