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慢性移植物抗宿主病:抗 T 细胞球蛋白 ATG-Fresenius 预防性应用或不应用于移植物抗宿主病预防的随机试验的长期结果。

Chronic graft-versus-host disease: long-term results from a randomized trial on graft-versus-host disease prophylaxis with or without anti-T-cell globulin ATG-Fresenius.

机构信息

Service d'Hématologie-Greffe de Moelle, Hôpital Saint Louis, Paris, France.

出版信息

Blood. 2011 Jun 9;117(23):6375-82. doi: 10.1182/blood-2011-01-329821. Epub 2011 Apr 5.

Abstract

Previous randomized graft-versus-host disease (GVHD)-prophylaxis trials have failed to demonstrate reduced incidence and severity of chronic GVHD (cGVHD). Here we reanalyzed and updated a randomized phase 3 trial comparing standard GVHD prophylaxis with or without pretransplantation ATG-Fresenius (ATG-F) in 201 adult patients receiving myeloablative conditioning before transplantation from unrelated donors. The cumulative incidence of extensive cGVHD after 3 years was 12.2% in the ATG-F group versus 45.0% in the control group (P < .0001). The 3-year cumulative incidence of relapse and of nonrelapse mortality was 32.6% and 19.4% in the ATG-F group and 28.2% and 33.5% in the control group (hazard ratio [HR] = 1.21, P = .47, and HR = 0.68, P = .18), respectively. This nonsignificant reduction in nonrelapse mortality without increased relapse risk led to an overall survival rate after 3 years of 55.2% in the ATG-F group and 43.3% in the control group (HR = 0.84, P = .39, nonsignificant). The HR for receiving immunosuppressive therapy (IST) was 0.31 after ATG-F (P < .0001), and the 3-year probability of survival free of IST was 52.9% and 16.9% in the ATG-F versus control, respectively. The addition of ATG-F to standard cyclosporine, methotrexate GVHD prophylaxis lowers the incidence and severity of cGVHD, and the risk of receiving IST without raising the relapse rate. ATG-F prophylaxis reduces cGVHD morbidity.

摘要

先前的随机移植物抗宿主病 (GVHD) 预防试验未能证明慢性 GVHD (cGVHD) 的发生率和严重程度降低。在这里,我们重新分析和更新了一项随机 3 期试验,该试验比较了在异基因供体造血细胞移植前接受清髓性预处理的 201 例成人患者中,标准 GVHD 预防与移植前应用抗胸腺细胞球蛋白 - 弗雷森纽斯 (ATG-F) 预防的效果。3 年后广泛 cGVHD 的累积发生率在 ATG-F 组为 12.2%,而对照组为 45.0%(P<0.0001)。ATG-F 组和对照组 3 年复发率和非复发死亡率分别为 32.6%和 19.4%,28.2%和 33.5%(风险比[HR] = 1.21,P =.47 和 HR = 0.68,P =.18)。非复发死亡率的这种无显著降低而复发风险无增加导致 ATG-F 组 3 年后总生存率为 55.2%,对照组为 43.3%(HR = 0.84,P =.39,无统计学意义)。ATG-F 后接受免疫抑制治疗(IST)的 HR 为 0.31(P<0.0001),ATG-F 组和对照组 3 年无 IST 生存的概率分别为 52.9%和 16.9%。在标准环孢素、甲氨蝶呤 GVHD 预防的基础上添加 ATG-F 可降低 cGVHD 的发生率和严重程度,并降低 IST 的风险而不增加复发率。ATG-F 预防可降低 cGVHD 的发病率。

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