Service de Médecine Interne et Unité INSERM U 976, Hôpital Saint-Louis, Assistance-Publique Hôpitaux de Paris, Paris-7 Université Denis Diderot, 1 avenue Claude Vellefaux, 75 010 Paris France.
Haematologica. 2010 Feb;95(2):284-92. doi: 10.3324/haematol.2009.013458. Epub 2009 Sep 22.
Autologous hematopoietic stem cell transplantation has been used since 1996 for the treatment of severe autoimmune diseases refractory to approved therapies. We evaluated the long-term outcomes of these transplants and aimed to identify potential prognostic factors.
In this observational study we analyzed all first autologous hematopoietic stem cell transplants for autoimmune diseases reported to the European Group for Blood and Marrow Transplantation (EBMT) registry between 1996-2007. The primary end-points for analysis were overall survival, progression-free survival and transplant-related mortality at 100 days.
Nine hundred patients with autoimmune diseases (64% female; median age, 35 years) who underwent a first autologous hematopoietic stem cell transplant were included. The main diseases were multiple sclerosis (n=345), systemic sclerosis (n=175), systemic lupus erythematosus (n=85), rheumatoid arthritis (n=89), juvenile arthritis (n=65), and hematologic immune cytopenia (n=37). Among all patients, the 5-year survival was 85% and the progression-free survival 43%, although the rates varied widely according to the type of autoimmune disease. By multivariate analysis, the 100-day transplant-related mortality was associated with the transplant centers' experience (P=0.003) and type of autoimmune disease (P=0.03). No significant influence of transplant technique was identified. Age less than 35 years (P=0.004), transplantation after 2000 (P=0.0015) and diagnosis (P=0.0007) were associated with progression-free survival.
This largest cohort studied worldwide shows that autologous hematopoietic stem cell transplantation can induce sustained remissions for more than 5 years in patients with severe autoimmune diseases refractory to conventional therapy. The type of autoimmune disease, rather than transplant technique, was the most relevant determinant of outcome. Results improved with time and were associated with the transplant centers' experience. These data support ongoing and planned phase III trials to evaluate the place of autologous hematopoietic stem cell transplantation in the treatment strategy for severe autoimmune diseases.
自 1996 年以来,自体造血干细胞移植已被用于治疗对已批准疗法有抗药性的严重自身免疫性疾病。我们评估了这些移植的长期结果,并旨在确定潜在的预后因素。
在这项观察性研究中,我们分析了 1996-2007 年间向欧洲血液和骨髓移植组(EBMT)登记处报告的所有用于治疗自身免疫性疾病的自体造血干细胞移植。分析的主要终点是 100 天的总生存率、无进展生存率和移植相关死亡率。
900 例患有自身免疫性疾病的患者(64%为女性;中位年龄为 35 岁)接受了首次自体造血干细胞移植。主要疾病为多发性硬化症(n=345)、系统性硬化症(n=175)、系统性红斑狼疮(n=85)、类风湿关节炎(n=89)、幼年特发性关节炎(n=65)和血液免疫性血细胞减少症(n=37)。在所有患者中,5 年生存率为 85%,无进展生存率为 43%,尽管根据自身免疫性疾病的类型,这些比率差异很大。通过多变量分析,100 天的移植相关死亡率与移植中心的经验(P=0.003)和自身免疫性疾病的类型(P=0.03)相关。未发现移植技术有显著影响。年龄小于 35 岁(P=0.004)、2000 年后移植(P=0.0015)和诊断(P=0.0007)与无进展生存率相关。
这项全球最大的队列研究表明,自体造血干细胞移植可在对常规治疗有抗药性的严重自身免疫性疾病患者中诱导持续缓解超过 5 年。自身免疫性疾病的类型,而不是移植技术,是最重要的预后决定因素。结果随着时间的推移而改善,并与移植中心的经验相关。这些数据支持正在进行和计划进行的 III 期试验,以评估自体造血干细胞移植在严重自身免疫性疾病治疗策略中的地位。