Kasper C, Terhaar A, Fosså A, Welt A, Seeber S, Nowrousian M R
Department of Internal Medicine (Cancer Research), West German Cancer Center, University of Essen Medical School, Germany.
Eur J Haematol. 1997 Apr;58(4):251-6. doi: 10.1111/j.1600-0609.1997.tb01663.x.
The efficacy and safety of recombinant human erythropoietin (rhEPO) were tested when given subcutaneously (s.c.) in an escalating dose of 2000-10,000 units (U) daily in 60 patients with cancer-related anaemia (CRA). A positive response, defined as an increase in haemoglobin more than 2 g/dl and independence of blood transfusions was observed in 23 of 48 evaluable patients (48%) within a median of 8 wk. In detail, rhEPO corrected anaemia in 11 of 14 patients (79%) with malignant lymphoma, in 8 of 15 patients (53%) with multiple myeloma and in 4 of 10 patients (40%) with a solid tumour. The median dose of rhEPO in successful cases was 5000 U daily. Four patients with agnogenic myeloid metaplasia and 5 with myelodysplastic disorder failed to respond to rhEPO. No patient had any severe side effects. Pretreatment serum erythropoietin levels appeared to be a weak predictor for response to rhEPO treatment. In conclusion, rhEPO seems to be safe and effective in correcting CRA in certain groups of patients.
对60例癌症相关性贫血(CRA)患者皮下注射重组人促红细胞生成素(rhEPO),剂量从每日2000单位(U)逐步递增至10000单位,以测试其疗效和安全性。48例可评估患者中有23例(48%)出现阳性反应,定义为血红蛋白增加超过2g/dl且无需输血,中位时间为8周。具体而言,rhEPO使14例恶性淋巴瘤患者中的11例(79%)、15例多发性骨髓瘤患者中的8例(53%)以及10例实体瘤患者中的4例(40%)贫血得到纠正。成功案例中rhEPO的中位剂量为每日5000U。4例原因不明的髓样化生患者和5例骨髓增生异常综合征患者对rhEPO无反应。无患者出现任何严重副作用。治疗前血清促红细胞生成素水平似乎是rhEPO治疗反应的弱预测指标。总之,rhEPO在纠正特定组患者的CRA方面似乎安全有效。