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同种异体造血干细胞移植治疗自身免疫性疾病:来自 EBMT 自身免疫性疾病工作组、免疫效应细胞工作组和移植后疾病工作组的回顾性研究。

Allogeneic HSCT for Autoimmune Diseases: A Retrospective Study From the EBMT ADWP, IEWP, and PDWP Working Parties.

机构信息

Unit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, Milan, Italy.

EBMT Paris Study Office/CEREST-TC - Department of Haematology, Saint Antoine Hospital - INSERM UMR 938 - Université Pierre et Marie Curie, Paris, France.

出版信息

Front Immunol. 2019 Jul 4;10:1570. doi: 10.3389/fimmu.2019.01570. eCollection 2019.

Abstract

This retrospective study assessed the use and long-term outcome of allogeneic hematopoietic stem cell transplantation (HSCT) in patients with severe autoimmune diseases (ADs), reported to the European Society for Blood and Marrow Transplantation (EBMT) registry. Between 1997 and 2014, 128 patients received allogeneic HSCT for various hematological ( = 49) and non-hematological ( = 79) refractory ADs. The median age was 12.7 years (0.2-62.2). Donors were syngeneic for seven, matched related for 46, unrelated for 51, haploidentical for 15, and cord blood for nine patients. The incidence of grades II-IV acute graft-vs.-host disease (GvHD) was 20.8% at 100 days. Cumulative incidence of chronic GvHD was 27.8% at 5-years. Non-relapse mortality (NRM) was 12.7% at 100-days. Overall survival (OS) and Progression-Free Survival (PFS) were 70.2 and 59.4% at 5-years, respectively. By multivariate analysis, age <18 years, males, and more recent year of transplant were found to be significantly associated with improved PFS. Reduced conditioning intensity was associated with a lower NRM. On a subgroup of 64 patients with detailed information a complete clinical response was obtained in 67% of patients at 1-year. This large EBMT survey suggests the potential of allogeneic HSCT to induce long-term disease control in a large proportion of refractory ADs, with acceptable toxicities and NRM, especially in younger patients.

摘要

这项回顾性研究评估了向欧洲血液和骨髓移植学会(EBMT)注册中心报告的患有严重自身免疫性疾病(AD)的患者接受同种异体造血干细胞移植(HSCT)的使用情况和长期结果。在 1997 年至 2014 年期间,有 128 名患者因各种血液学(= 49)和非血液学(= 79)难治性 AD 接受了同种异体 HSCT。中位年龄为 12.7 岁(0.2-62.2)。7 例为同基因供体,46 例为匹配相关供体,51 例为无关供体,15 例为半相合供体,9 例为脐血供体。100 天时,II-IV 级急性移植物抗宿主病(GvHD)的发生率为 20.8%。5 年时慢性 GvHD 的累积发生率为 27.8%。100 天的非复发死亡率(NRM)为 12.7%。5 年时的总生存率(OS)和无进展生存率(PFS)分别为 70.2%和 59.4%。多变量分析显示,年龄<18 岁、男性和移植年份更新与 PFS 改善显著相关。预处理强度降低与 NRM 降低相关。在有详细信息的 64 名患者亚组中,1 年内有 67%的患者获得完全临床缓解。这项大型 EBMT 调查表明,同种异体 HSCT 有可能在很大一部分难治性 AD 中诱导长期疾病控制,具有可接受的毒性和 NRM,尤其是在年轻患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6457/6622152/35c45f8cb4c2/fimmu-10-01570-g0001.jpg

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