Jacobs P, Wood L, Martell R W
Br J Haematol. 1985 Oct;61(2):267-72. doi: 10.1111/j.1365-2141.1985.tb02825.x.
Twelve consecutive adults with severe acute aplastic anaemia, not having a bone marrow transplantation option, were prospectively randomized to receive either cyclosporin A alone or an equivalent amount of this immunosuppressive agent in combination with antilymphocyte serum. The minimum follow-up is 36 months, with half the patients developing nephrotoxicity, which was easily reversible in all but one. No response could be attributed to either regimen. Cyclosporin A does not appear to have a place as primary form of treatment for adults with severe acute aplastic anaemia, either on its own or in combination with antilymphocyte serum.
12例患有严重急性再生障碍性贫血且没有骨髓移植选择的成年患者被前瞻性随机分组,分别单独接受环孢素A或等量的这种免疫抑制剂与抗淋巴细胞血清联合治疗。最短随访时间为36个月,半数患者出现肾毒性,除1例患者外其余患者的肾毒性均易于逆转。两种治疗方案均未显示出疗效。对于患有严重急性再生障碍性贫血的成年人,环孢素A无论是单独使用还是与抗淋巴细胞血清联合使用,似乎都不适合作为主要治疗方式。