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Cisplatin-associated anaemia treated with subcutaneous erythropoietin. A pilot study

机译:皮下促红细胞生成素治疗顺铂相关性贫血。初步研究

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In 20 patients with cisplatin-associated anaemia (haemoglobin less than 90 gl-1), recombinant human erythropoietin was administered subcutaneously three times a week on an outpatient basis. The initial dose was 50 Units Kg-1 of body weight. If response was not achieved within 3 weeks, dose was increased to 75 Units Kg-1. Using the same criteria further escalation to 100 Units Kg-1 was performed. If there was no response erythropoietin was terminated. Fifteen patients obtained an increase in haemoglobin to above 100 gl-1 which was considered as a clinical response in this study, with a dose of 50 Units Kg-1; one patient needed an erythropoietin dose of 75 Units Kg-1 and one a dose of 100 Units Kg-1. Only three patients required haemotransfusions and were considered non responders. Haemoglobin increases occurred despite continuation of cisplatin chemotherapy. In conclusion subcutaneous low dose of erythropoietin seems to be effective and safe in the treatment of cisplatin-induced anaemia.
机译:在20名顺铂相关性贫血(血红蛋白低于90 gl-1)患者中,重组人促红细胞生成素在门诊患者每周皮下给药3次。初始剂量为50单位体重Kg-1。如果在3周内未达到反应,则剂量应增加至75单位Kg-1。使用相同的标准,进一步升级为100单位Kg-1。如果没有反应,则促红细胞生成素终止。 15例患者的血红蛋白增加至100 gl-1以上,在本研究中被认为是临床反应,剂量为50单位Kg-1。一名患者需要75单位Kg-1的促红细胞生成素剂量,另一名患者需要100单位Kg-1的促红细胞生成素剂量。仅三名需要输血的患者被视为无反应。尽管继续进行顺铂化疗,仍发生血红蛋白增加。总之,皮下低剂量促红细胞生成素在治疗顺铂引起的贫血方面似乎是有效和安全的。

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