Autologous haematopoiesis stem cell transplantation (AHSCT) for treatment-refractory autoimmune diseases in children

IF 5.1 2区 医学 Q1 RHEUMATOLOGY RMD Open Pub Date : 2024-07-01 DOI:10.1136/rmdopen-2024-004381
Özlem Satirer, Joerg C Henes, Michaela Döring, Till Lesk, Susanne Benseler, Jasmin Beate Kuemmerle-Deschner
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Abstract

Objectives To evaluate the long-term effectiveness and safety of autologous haematopoiesis stem cell transplantation (AHSCT) for severe, refractory autoimmune diseases in paediatric patients. Methods A single-centre study of consecutive children and adolescents with refractory autoimmune diseases undergoing AHSCT was performed. Demographics, clinical, laboratory features, pre-AHSCT medications, disease activity and functional status were captured. The primary outcome was progression-free survival, secondary outcomes included overall survival, disease-specific treatment responses, disease activity at the last follow-up and AHSCT safety. Results The study included seven patients: two systemic sclerosis, one pansclerotic morphoea, one eosinophilic fasciitis, one juvenile dermatomyositis and two patients with systemic juvenile idiopathic arthritis; four women, three men median age at AHSCT of 10 years (7–19), median follow-up post-AHSCT of 17 years. Median progression-free survival and overall survival was 4.2 years (95% CI: 0.98 to 8.3) and 17 years (95% CI: 11.8 to 22.1), respectively. Progression-free survival rates at 1 and 2 years post-AHSCT were 100% and 77%, respectively. All children survived. All patients are in clinical remission, only four require ongoing immunotherapy. Safety: Three experienced infections, including HHV6, Candida and Ralstonia sepsis; one developed a systemic inflammatory response syndrome; two new onset secondary autoimmune diseases including autoimmune haemolytic anaemia, Graves’ disease and one was found to have a breast fibroadenoma. Treatment toxicity: one cyclophosphamide-associated transient renal failure and pericardial effusion, one patient with amenorrhoea/infertility. Conclusions AHSCT was an effective and safe approach for children and adolescents with treatment-refractory autoimmune diseases. The indication and timing of transplantation requires a careful consideration and a multidisciplinary approach. Data are available upon reasonable request.
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自体造血干细胞移植(AHSCT)治疗儿童难治性自身免疫性疾病
目的 评估自体造血干细胞移植(AHSCT)治疗严重难治性自身免疫性疾病的长期有效性和安全性。方法 对连续接受自体造血干细胞移植的难治性自身免疫性疾病儿童和青少年进行单中心研究。研究记录了患者的人口统计学特征、临床和实验室特征、AHSCT 前的用药情况、疾病活动和功能状态。主要结果是无进展生存期,次要结果包括总生存期、疾病特异性治疗反应、最后一次随访时的疾病活动性和 AHSCT 的安全性。结果 该研究包括七名患者:两名系统性硬化症患者、一名泛硬化性变形症患者、一名嗜酸性粒细胞筋膜炎患者、一名幼年皮肌炎患者和两名系统性幼年特发性关节炎患者;其中四名女性,三名男性,AHSCT时的中位年龄为10岁(7-19岁),AHSCT后的中位随访时间为17年。无进展生存期和总生存期的中位数分别为4.2年(95% CI:0.98-8.3)和17年(95% CI:11.8-22.1)。AHSCT后1年和2年的无进展生存率分别为100%和77%。所有患儿均存活。所有患者均临床缓解,只有四名患者需要持续接受免疫治疗。安全性:三名患者出现感染,包括HHV6、白色念珠菌和拉氏菌败血症;一名患者出现全身炎症反应综合征;两名患者新发继发性自身免疫性疾病,包括自身免疫性溶血性贫血和巴塞杜氏病;一名患者被发现患有乳腺纤维腺瘤。治疗毒性:一名患者出现环磷酰胺相关的一过性肾衰竭和心包积液,一名患者闭经/不孕。结论 对于患有难治性自身免疫性疾病的儿童和青少年来说,AHSCT是一种有效而安全的方法。移植的适应症和时机需要仔细考虑,并采用多学科方法。如有合理要求,可提供相关数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
RMD Open
RMD Open RHEUMATOLOGY-
CiteScore
7.30
自引率
6.50%
发文量
205
审稿时长
14 weeks
期刊介绍: RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.
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