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门诊氟达拉滨、环磷酰胺和利妥昔单抗联合异基因造血细胞移植治疗成人重型再生障碍性贫血的疗效和安全性。

Efficacy and safety of outpatient fludarabine, cyclophosphamide, and rituximab based allogeneic hematopoietic cell transplantation in adults with severe aplastic anemia.

机构信息

Cleveland Clinic, Department of Pharmacy, Cleveland, OH, USA.

Sarah Cannon Cancer Center, TriStar Centennial Medical Center, Nashville, TN, USA.

出版信息

Bone Marrow Transplant. 2024 Sep;59(9):1275-1279. doi: 10.1038/s41409-024-02323-1. Epub 2024 Jun 15.

Abstract

The age effect in severe aplastic anemia (SAA) following allogeneic hematopoietic cell transplantation (HCT) favors the use of reduced intensity conditioning (RIC) regimens in older adults. We implemented a non-myeloablative regimen consisting of fludarabine, cyclophosphamide, and rituximab (FCR) to improve HCT outcomes in SAA. Patients who underwent first HCT for SAA utilizing an FCR regimen between January 2016 and May 2022 were included. Outcomes analyzed included time to engraftment, incidence of graft failure, GVHD, viral reactivation, disease recurrence, and GVHD-free, relapse-free survival (GRFS). Among 24 patients included, median age was 43.5 years (22-62) and a variety of donor types and stem cell sources were represented. At median follow-up of 26.9 months (2.4-72.7), no cases of grade III-IV acute (aGVHD) or severe chronic GVHD (cGVHD) were recorded. Viral reactivation was minimal, and there were no cases of graft failure or PTLD, with 100% disease-free and overall survival at last follow up. The estimate of 1-year GRFS was 86.3% (95% CI: 72.8-100%), with moderate cGVHD accounting for all events. The FCR regimen in SAA was well tolerated, even in older adults, with 100% disease-free survival with low GVHD and infection rates. These encouraging findings should be validated in larger prospective trials.

摘要

异基因造血细胞移植(HCT)后重型再生障碍性贫血(SAA)的年龄效应有利于在老年患者中使用强度降低的预处理方案。我们实施了一种非清髓性方案,包括氟达拉滨、环磷酰胺和利妥昔单抗(FCR),以改善 SAA 患者的 HCT 结局。本研究纳入了 2016 年 1 月至 2022 年 5 月期间接受首次 FCR 方案治疗的 SAA 患者。分析的结果包括植入时间、移植物失败、移植物抗宿主病(GVHD)、病毒再激活、疾病复发以及无 GVHD 无复发生存(GRFS)。在纳入的 24 例患者中,中位年龄为 43.5 岁(22-62 岁),代表了各种供体类型和干细胞来源。中位随访 26.9 个月(2.4-72.7),未记录到 3-4 级急性(aGVHD)或严重慢性 GVHD(cGVHD)。病毒再激活很少,无移植物失败或 PTLD 病例,末次随访时 100%无疾病和总生存。估计 1 年 GRFS 为 86.3%(95%CI:72.8-100%),所有事件均由中度 cGVHD 引起。即使在老年患者中,FCR 方案治疗 SAA 也具有良好的耐受性,GVHD 和感染率低,无疾病生存 100%。这些令人鼓舞的发现应该在更大的前瞻性试验中得到验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c162/11368812/dac31e44d47a/41409_2024_2323_Fig1_HTML.jpg

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