Spicka I, Svára F, Novosadová L, Mácel I, Válková V, Sulková S, Merta M, Klener P
I.interní klinika 1.lékarské fakulty Univerzity Karlovy a Vseobecné fakultní nemocnice v Praze, Praha, Czech Republic.
Sb Lek. 1997;98(2):127-33.
The efficacy of recombinant human erythropoietin (r-HuEPO) in patients with multiple myeloma (MM) has been confirmed in several clinical trials. We report our experience of r-HuEPO treatment in 5 myeloma patients with renal failure. The therapy with r-HuEPO (Eprex, Janssen-Cilag or Recormon, Boehringer, Mannheim) was started after 4-8 months from diagnosis, the drug was administered intravenously (in one patient subcutaneously after cessation of hemodialysis treatment), two or three times weekly. The initial doses were 4-12,000 units/week (mean 8,400). In all patients good response during the first month of therapy was observed. Median Hb and hematocrit increased from 70 g/l and 20.8% to 87 g/l and 26% after 1 month and to 105 g/l and 30.3% after 4-6 months, respectively. The need for blood transfusion decreased significantly--from 2.72 TU/month to 0.13 TU/month. WHO performance status and patients self-assessment of quality of live improved substantially after r-HuEPO. No serious adverse events, including hypertension and/or thromboembolic events were observed. In accordance with some previous reports we conclude r-HuEPO is effective and safe treatment in patients with MM and renal failure. Moreover, lower doses of growth factor could be effective in this particular group of patients.
重组人促红细胞生成素(r-HuEPO)在多发性骨髓瘤(MM)患者中的疗效已在多项临床试验中得到证实。我们报告了5例骨髓瘤合并肾衰竭患者接受r-HuEPO治疗的经验。r-HuEPO(益比奥,杨森-西拉格公司生产;或利血宝,勃林格殷格翰公司生产)治疗在确诊后4至8个月开始,药物通过静脉给药(1例患者在停止血液透析治疗后皮下给药),每周两到三次。初始剂量为4000至12000单位/周(平均8400单位)。所有患者在治疗的第一个月均观察到良好反应。治疗1个月后,血红蛋白(Hb)中位数和血细胞比容分别从70g/L和20.8%升至87g/L和26%,4至6个月后分别升至105g/L和30.3%。输血需求显著下降——从每月2.72单位降至每月0.13单位。r-HuEPO治疗后,世界卫生组织(WHO)的体能状态评分和患者对生活质量的自我评估均有显著改善。未观察到严重不良事件,包括高血压和/或血栓栓塞事件。根据之前的一些报告,我们得出结论,r-HuEPO对MM合并肾衰竭患者是一种有效且安全的治疗方法。此外,较低剂量的生长因子对这一特定患者群体可能有效。