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阿巴西普预防移植物抗宿主病可降低伴用白消安、氟达拉滨和噻替哌的异基因造血干细胞移植治疗重型β地中海贫血的严重急性移植物抗宿主病。

Graft-versus-host Disease Prophylaxis With Abatacept Reduces Severe Acute Graft-versus-host Disease in Allogeneic Hematopoietic Stem Cell Transplant for Beta-thalassemia Major With Busulfan, Fludarabine, and Thiotepa.

机构信息

Division of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

Division of Pharmacology, Seattle Cancer Care Alliance and Fred Hutchinson Cancer Research Center, Seattle, WA.

出版信息

Transplantation. 2021 Apr 1;105(4):891-896. doi: 10.1097/TP.0000000000003327.

Abstract

BACKGROUND

We hypothesized that the addition of 4 doses of abatacept to our standard acute graft-versus-host disease (GVHD) prophylaxis would reduce the incidence of day +100 severe acute GVHD in children with transfusion-dependent beta-thalassemia major undergoing a myeloablative allogeneic hematopoietic stem cell transplant (HSCT), without impacting engraftment.

METHODS

Twenty-four children with beta-thalassemia major received abatacept at a dose of 10 mg/kg intravenously on days -1, +5, +14, and +28 after HSCT in addition to calcineurin inhibitors and methylprednisolone. Outcomes were compared to 8 beta-thalassemia patients who received standard acute GVHD prophylaxis.

RESULTS

There was no difference in engraftment between the 2 groups. No patient had grades III-IV acute GVHD by day +100 in the abatacept cohort compared with 50% in the standard acute GVHD prophylaxis group (P = 0.001). Viral reactivation occurred in 5 children in the standard acute GVHD cohort and in 20 children in the abatacept cohort (P = 0.2). Thalassemia-free survival after HSCT was 100% in the abatacept cohort compared to 62.5% in the standard cohort at last follow-up (P = 0.007).

CONCLUSIONS

Adding abatacept to our routine GVHD prophylaxis reduced the incidence of day +100 severe acute GVHD without impacting engraftment or survival.

摘要

背景

我们假设在我们标准的急性移植物抗宿主病(GVHD)预防方案中添加 4 剂阿巴西普,可以降低输血依赖型重型β地中海贫血儿童接受清髓性异基因造血干细胞移植(HSCT)后第 100 天重度急性 GVHD 的发生率,而不会影响植入。

方法

24 例重型β地中海贫血儿童在 HSCT 后第-1、+5、+14 和+28 天,接受阿巴西普 10mg/kg 静脉注射,同时接受钙调神经磷酸酶抑制剂和甲基强的松龙。将这些结果与接受标准急性 GVHD 预防方案的 8 例β地中海贫血患者进行比较。

结果

两组间的植入无差异。阿巴西普组在第 100 天无 III-IV 级急性 GVHD 患者,而标准急性 GVHD 预防组为 50%(P=0.001)。标准急性 GVHD 预防组有 5 例患儿出现病毒再激活,而阿巴西普组有 20 例患儿出现病毒再激活(P=0.2)。在最后一次随访时,阿巴西普组 HSCT 后无地中海贫血生存为 100%,而标准组为 62.5%(P=0.007)。

结论

在我们常规的 GVHD 预防方案中添加阿巴西普可降低第 100 天重度急性 GVHD 的发生率,而不影响植入和生存。

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