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原发性噬血细胞性淋巴组织细胞增生症的异基因造血干细胞移植:单中心经验。

Allogeneic stem cell transplant in primary hemophagocytic lymphohistiocytosis - a single-center experience.

机构信息

Armed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.

出版信息

Ann Hematol. 2024 Sep;103(9):3775-3782. doi: 10.1007/s00277-024-05890-x. Epub 2024 Jul 24.

Abstract

Hemophagocytic Lymphohistiocytosis (HLH) is a rare disorder of immune dysregulation characterized by fever, cytopenias, and splenomegaly. Its primary form poses a therapeutic challenge due to its high fatality when left untreated. We retrospectively analyzed 28 patients who underwent related-donor allogeneic stem cell transplant for primary HLH from 2010 to 2021. Among them were 10 cases of familial HLH, 8 cases of Griscelli syndrome type 2, and 1 case each with PRF1 and STX11 mutations. All the patients underwent transplants with reduced-intensity or myeloablative conditioning and 26 of them achieved neutrophil engraftment at a median of day + 14. The donors were either fully matched (68%) or haploidentical (32%). With a median follow-up of 1 year, overall survival was 68% (n = 19) and disease-free survival was 64.4% (n = 18). OS was better in patients transplanted with a sibling donor (compared to parent donor), who achieved complete donor chimerism, and those transplanted early in the course of the disease (diagnosis to transplant duration less than 6 months).

摘要

噬血细胞性淋巴组织细胞增生症(HLH)是一种罕见的免疫失调疾病,其特征为发热、血细胞减少和脾肿大。由于未经治疗时病死率高,其原发性形式具有治疗挑战性。我们回顾性分析了 2010 年至 2021 年间接受相关供体同种异体干细胞移植治疗原发性 HLH 的 28 例患者。其中 10 例为家族性 HLH,8 例为 Griscelli 综合征 2 型,1 例分别为 PRF1 和 STX11 突变。所有患者均接受了强度降低或清髓性预处理的移植,其中 26 例在中位数为第 14 天实现了中性粒细胞植入。供体为完全匹配(68%)或半相合(32%)。中位随访 1 年后,总生存率为 68%(n=19),无病生存率为 64.4%(n=18)。与接受父母供体(与同胞供体相比)、达到完全供体嵌合以及在疾病早期(诊断至移植时间<6 个月)接受移植的患者相比,OS 更好。

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