Ruutu T, Volin L, Tenhunen R
Br J Haematol. 1987 Apr;65(4):425-8. doi: 10.1111/j.1365-2141.1987.tb04144.x.
We report on two patients with a myelodysplastic syndrome in whom the blood cell counts markedly improved during treatment with haem arginate. One patient received haem arginate only, the other haem arginate in combination with low dose androgen. The drug was given as weekly infusions of 2-3 mg/kg body weight for 8-12 weeks. In one patient the percentage of ringed and other abnormal sideroblasts in the bone marrow was clearly reduced as a result of the treatment. In both patients the effect on blood cell counts lasted for several months after the cessation of the haem arginate treatment. Eleven other patients showed no clear response. No adverse effects of the infusions were observed. Further studies on the possible therapeutic role of haem arginate are indicated.
我们报告了两名骨髓增生异常综合征患者,他们在接受精氨酸血红素治疗期间血细胞计数显著改善。一名患者仅接受精氨酸血红素治疗,另一名患者则接受精氨酸血红素与低剂量雄激素联合治疗。药物通过每周静脉输注2 - 3mg/kg体重,持续8 - 12周。治疗后,一名患者骨髓中环形及其他异常铁粒幼细胞的百分比明显降低。两名患者在精氨酸血红素治疗停止后,血细胞计数改善的效果持续了数月。其他11名患者未显示出明显反应。未观察到输注的不良反应。有必要对精氨酸血红素可能的治疗作用进行进一步研究。