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镰状细胞病异基因匹配相关供者造血细胞移植所用方案的比较。

Comparison of Regimens Used for Allogeneic Matched Related Donor Hematopoietic Cell Transplantation for Sickle Cell Disease.

作者信息

Prior Daniel, Liang Jingchen, Deng Yanhong, Shah Niketa, Flagg Aron, Krishnamurti Lakshmanan

机构信息

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut.

Yale School of Public Health, New Haven, Connecticut.

出版信息

Transplant Cell Ther. 2025 Aug;31(8):594.e1-594.e13. doi: 10.1016/j.jtct.2025.05.004. Epub 2025 May 14.

Abstract

Prior analyses have reported on the impact of different donor types and conditioning regimen intensities on outcomes for patients with sickle cell disease (SCD) who undergo hematopoietic cell transplantation (HCT), and demonstrated superior outcomes using an HLA-matched related donor (MRD). However, the impact of conditioning regimen intensity on outcomes remains unclear, with conflicting findings across studies. In addition, the lack of data on comparative outcomes of different approaches to conditioning and graft-versus-host disease (GVHD) prophylaxis for allogeneic HCT for SCD remains a gap in the field. We compared outcomes for SCD patients who have received HLA-matched related donor (MRD) HCT for SCD using different HCT regimens. We examined de-identified records of MRD HCT for SCD on patients transplanted between 1991 and 2022 in the United States and submitted to the CIBMTR. We compared the most common transplant regimens in the registry, which included TBI 300/400 cGy + sirolimus + anti-thymocyte globulin (ATG)/alemtuzumab described by Hsieh et al; Busulfan/Fludarabine + CNI/methotrexate (MTX) + ATG/alemtuzumab as described by Krishnamurti et al.; Fludarabine/Melphalan + CNI/MTX + ATG/alemtuzumab as described by King et al.; and Busulfan/Cyclophosphamide (CY) + CNI /MTX/prednisone + ATG/alemtuzumab as described by Walters et al. For pediatric MRD HCT, EFS rates were highest with the Krishnamurti et al. (3-year EFS 94%, 95% CI 88, 100) and lowest with the Hsieh et al. regimen (3-year EFS 57%, 95% CI 25, 100, p<0.001). Rates of chronic GVHD were lowest in the Hsieh et al. cohort (3-year rate 0%) and highest in the King et al. cohort (3-year rate 20.4%, 95% CI 13.2, 28.8, p=0.040). For adult MRD HCT, EFS rates were similar between the Hsieh et al. and Krishnamurti et al. regimens, while cGVHD was significantly lower in the Hsieh et al. cohort. These real-world data have the potential to inform shared decision-making in MRD HCT for SCD. Pediatric patients had the highest EFS rates using myeloablative conditioning regimens, while non-myeloablative conditioning resulted in the lowest EFS rates. Adult patients had similar event-free survival using myeloablative and non-myeloablative conditioning regimens, with less GVHD following non-myeloablative regimens.

摘要

先前的分析报告了不同供体类型和预处理方案强度对接受造血细胞移植(HCT)的镰状细胞病(SCD)患者结局的影响,并证明使用人类白细胞抗原(HLA)匹配的相关供体(MRD)可获得更好的结局。然而,预处理方案强度对结局的影响仍不明确,各研究结果相互矛盾。此外,对于SCD异基因HCT中不同预处理方法和移植物抗宿主病(GVHD)预防措施的比较结局缺乏数据,这仍是该领域的一个空白。我们比较了使用不同HCT方案接受HLA匹配相关供体(MRD)HCT治疗SCD患者的结局。我们查阅了1991年至2022年在美国接受移植并提交至CIBMTR的SCD患者MRD HCT的去识别记录。我们比较了登记处最常见的移植方案,包括Hsieh等人描述的全身照射(TBI)300/400 cGy+西罗莫司+抗胸腺细胞球蛋白(ATG)/阿仑单抗;Krishnamurti等人描述的白消安/氟达拉滨+钙调神经磷酸酶抑制剂(CNI)/甲氨蝶呤(MTX)+ATG/阿仑单抗;King等人描述的氟达拉滨/美法仑+CNI/MTX+ATG/阿仑单抗;以及Walters等人描述的白消安/环磷酰胺(CY)+CNI/MTX/泼尼松+ATG/阿仑单抗。对于儿童MRD HCT,Krishnamurti等人方案的无事件生存率(EFS)最高(3年EFS为94%,95%置信区间[CI]为88,100),而Hsieh等人方案的EFS最低(3年EFS为57%,95%CI为25,100,p<0.001)。慢性GVHD发生率在Hsieh等人队列中最低(3年发生率为0%),在King等人队列中最高(3年发生率为20.4%,95%CI为13.2,28.8,p=0.040)。对于成人MRD HCT,Hsieh等人和Krishnamurti等人方案的EFS率相似,而Hsieh等人队列中的慢性GVHD明显更低。这些真实世界的数据有可能为SCD患者MRD HCT的共同决策提供参考。儿童患者使用清髓性预处理方案时EFS率最高,而非清髓性预处理导致EFS率最低。成人患者使用清髓性和非清髓性预处理方案时无事件生存率相似,非清髓性方案后的GVHD更少。

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