Qiao Z H
Second Affiliated Hospital of Shanxi Medical College, Taiyuan.
Zhonghua Zhong Liu Za Zhi. 1993 Mar;15(2):122-4.
Anemia is a common complication of patients with multiple myeloma (MM) and myelodysplastic syndrome (MDS). Most of these patients often require blood transfusion. 12 patients, including 7 cases of MM and 5 cases of MDS, were treated with rhEPO 10,000 micrograms three times a week for 15 weeks. The hemoglobin in 6 of 7 cases of MM steadily increased and eventually reached normal level without blood transfusion. The number of erythroid precursors in bone marrow was increased significantly and serum ferritin concentration was decreased gradually during EPO administration. However 5 patients with MDS did not show any response to EPO. The adverse side effects were hardly observed in any patients received EPO treatment. It is suggested that rhEPO is a promising preparation for treating MM-associated anemia rather than MDS-associated anemia.
贫血是多发性骨髓瘤(MM)和骨髓增生异常综合征(MDS)患者的常见并发症。这些患者中的大多数常常需要输血。12例患者,包括7例MM和5例MDS患者,接受了重组人促红细胞生成素(rhEPO)治疗,剂量为每周3次,每次10000微克,共治疗15周。7例MM患者中有6例血红蛋白稳步上升,最终达到正常水平,无需输血。在使用EPO期间,骨髓中红系前体细胞数量显著增加,血清铁蛋白浓度逐渐降低。然而,5例MDS患者对EPO没有任何反应。接受EPO治疗的任何患者几乎都未观察到不良反应。提示rhEPO是治疗MM相关性贫血而非MDS相关性贫血的一种有前景的制剂。