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人类同种异体骨髓移植受者移植物抗宿主病的治疗:一项比较抗胸腺细胞球蛋白和皮质类固醇的随机试验。

Treatment of graft-versus-host disease in human allogeneic marrow graft recipients: a randomized trial comparing antithymocyte globulin and corticosteroids.

作者信息

Doney K C, Weiden P L, Storb R, Thomas E D

出版信息

Am J Hematol. 1981;11(1):1-8. doi: 10.1002/ajh.2830110102.

Abstract

This prospective randomized trial compared the effect of antihuman thymocyte globulin (ATG) versus corticosteroids as treatment of graft-versus-host disease (GVHD) in recipients of HLA-identical allogeneic bone marrow transplants. Patients undergoing transplantation as therapy for either hematologic malignancies or aplastic anemia were given methotrexate as postgrafting immunosuppression. Patients who nevertheless developed acute GVHD of moderate severity were randomized to receive either corticosteroid therapy or ATG therapy. Thirty-seven patients were randomized: 20 patients received corticosteroids, and 17 received ATG. Both ATG and corticosteroids were in general well tolerated, although all patients receiving ATG developed fever and chills. Both treatment modalities were associated with a mild decrease in severity of GVHD after therapy. There was, however, no significant difference between treatment groups, whether assessed by improvement in specific organ involvement, improvement in the overall grade of GVHD, need for additional therapy for acute GVHD, or the proportion of patients who developed chronic GVHD. Infectious complications and survival were also not different between treatment groups. Thus, corticosteroids were as effective as ATG for the treatment of acute GVHD in recipients of HLA-identical marrow transplants and, therefore, appear to be a reasonable choice as primary therapy for acute GVHD.

摘要

这项前瞻性随机试验比较了抗人胸腺细胞球蛋白(ATG)与皮质类固醇对 HLA 同基因异基因骨髓移植受者移植物抗宿主病(GVHD)的治疗效果。接受移植治疗血液系统恶性肿瘤或再生障碍性贫血的患者,在移植后接受甲氨蝶呤作为免疫抑制治疗。然而,发生中度急性 GVHD 的患者被随机分为接受皮质类固醇治疗或 ATG 治疗。37 名患者被随机分组:20 名患者接受皮质类固醇治疗,17 名接受 ATG 治疗。尽管所有接受 ATG 治疗的患者都出现了发热和寒战,但 ATG 和皮质类固醇总体上耐受性良好。两种治疗方式在治疗后 GVHD 严重程度均有轻度降低。然而,无论是通过特定器官受累情况的改善、GVHD 总体分级的改善、急性 GVHD 是否需要额外治疗,还是发生慢性 GVHD 的患者比例来评估,治疗组之间均无显著差异。治疗组之间的感染并发症和生存率也没有差异。因此,皮质类固醇在治疗 HLA 同基因骨髓移植受者的急性 GVHD 方面与 ATG 同样有效,因此,似乎是急性 GVHD 初始治疗的合理选择。

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