首页> 美国卫生研究院文献>other >Allogeneic HSCT for Autoimmune Diseases: A Retrospective Study From the EBMT ADWP IEWP and PDWP Working Parties
【2h】

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

机译:自身免疫性疾病的异基因HSCT:EBMT ADWPIEWP和PDWP工作组的回顾性研究

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

>Background: 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.>Methods: Between 1997 and 2014, 128 patients received allogeneic HSCT for various hematological (n = 49) and non-hematological (n = 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.>Results: 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.>Conclusions: 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.
机译:>背景:这项回顾性研究评估了同种异体造血干细胞移植(HSCT)在重度自身免疫性疾病(AD)患者中的使用和长期结果,该报道已向欧洲血液和骨髓移植学会( >方法::在1997年至2014年之间,有128例因各种血液学(n = 49)和非血液学(n = 79)难治性AD接受了异基因HSCT。中位年龄为12.7岁(0.2-62.2)。供体为7个同系,配对为46个,不相关为51个,单倍体为15个,脐带血为9例。>结果:II-IV级急性移植物抗宿主病的发生率(GvHD)在100天时为20.8%。五年中慢性GvHD的累积发生率为27.8%。 100天的非复发死亡率(NRM)为12.7%。 5年总生存(OS)和无进展生存(PFS)分别为70.2%和59.4%。通过多变量分析,发现年龄小于18岁,男性和较新的移植年份与PFS改善显着相关。调节强度降低与NRM降低有关。在64位具有详细信息的患者亚组中,在1年时67%的患者获得了完整的临床反应。>结论:这项大型EBMT调查表明,同种异体HSCT可能诱发长期疾病可以控制大部分难治性AD,具有可接受的毒性和NRM,尤其是在年轻患者中。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号