Storb R, Deeg H J, Farewell V, Doney K, Appelbaum F, Beatty P, Bensinger W, Buckner C D, Clift R, Hansen J
Blood. 1986 Jul;68(1):119-25.
Forty-six patients with severe aplastic anemia (median age, 23 years) were treated with high-dose cyclophosphamide followed by infusion of marrow from an HLA-identical family member. To evaluate postgrafting prophylaxis for graft-v-host disease (GVHD), they were entered into a prospective randomized trial comparing the effect of a combination of methotrexate and cyclosporine (n = 22) to that of methotrexate alone (n = 24). Forty-four of the forty-six patients had evidence of sustained marrow engraftment. Only one patient in each of the two study groups showed graft rejection. A significant reduction in the cumulative incidence of grades II to IV acute GVHD was seen in patients given methotrexate/cyclosporine (18%) compared with those given methotrexate alone (53%) (P = .012). In three patients given methotrexate alone, grade III developed, and in six, grade IV acute GVHD developed, compared with none given methotrexate/cyclosporine. Eighteen of the 22 patients given methotrexate/cyclosporine and 15 of the 24 given methotrexate alone are alive between 5.5 and 44.5 months (median, 18 months), with actuarial survival rates at 2 years of 82% and 60%, respectively (P = .062). The incidence of fatal infections was higher in patients given methotrexate alone, whereas there are as yet no significant differences in the incidence of chronic GVHD. We conclude that methotrexate/cyclosporine treatment resulted in a significant decrease in the incidence and severity of acute GVHD in patients who received transplants for severe aplastic anemia and thus an improvement in survival.
46例严重再生障碍性贫血患者(中位年龄23岁)接受了大剂量环磷酰胺治疗,随后输注来自HLA匹配的家庭成员的骨髓。为了评估移植后预防移植物抗宿主病(GVHD)的效果,他们进入了一项前瞻性随机试验,比较甲氨蝶呤和环孢素联合使用(n = 22)与单独使用甲氨蝶呤(n = 24)的效果。46例患者中有44例有持续骨髓植入的证据。两个研究组中各只有1例患者出现移植排斥。与单独使用甲氨蝶呤的患者(53%)相比,接受甲氨蝶呤/环孢素治疗的患者中,II至IV级急性GVHD的累积发生率显著降低(18%)(P = 0.012)。单独使用甲氨蝶呤的3例患者发生了III级GVHD,6例发生了IV级急性GVHD,而接受甲氨蝶呤/环孢素治疗的患者均未出现。接受甲氨蝶呤/环孢素治疗的22例患者中有18例,单独使用甲氨蝶呤的24例患者中有15例在5.5至44.5个月(中位时间18个月)存活,2年的实际生存率分别为82%和60%(P = 0.062)。单独使用甲氨蝶呤的患者中致命感染的发生率较高,而慢性GVHD的发生率尚无显著差异。我们得出结论,甲氨蝶呤/环孢素治疗可使接受严重再生障碍性贫血移植的患者急性GVHD的发生率和严重程度显著降低,从而提高生存率。