Inflammatory Bowel Disease Unit, Gastroenterology Department. Hospital Clínic Barcelona, Fundació Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer [IDIBAPS], Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas [CIBEREHD], Barcelona, Catalonia, Spain.
Bone Marrow Transplantation Unit, Haematology Department, Institute of Haematology and Oncology Hospital Clínic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer [IDIBAPS], University of Barcelona, Josep Carreras Leukaemia Research Foundation, Barcelona, Catalonia, Spain.
J Crohns Colitis. 2024 Oct 15;18(10):1701-1712. doi: 10.1093/ecco-jcc/jjae076.
Autologous haematopoietic stem cell transplantation [AHSCT] is a therapeutic option for refractory Crohn's disease [CD]. However, high adverse event rates related to chemotherapy toxicity and immunosuppression limit its applicability. This study aims to evaluate AHSCT's safety and efficacy using a cyclophosphamide [Cy]-free mobilisation regimen.
A prospective, observational study included 14 refractory CD patients undergoing AHSCT between June 2017 and October 2022. The protocol involved outpatient mobilisation with G-CSF 12-16 μg/kg/daily for 5 days, and optional Plerixafor 240 μg/d [1-2 doses] if the CD34 + cell count target was unmet. Standard conditioning with Cy and anti-thymocyte globulin was administered. Clinical, endoscopic, and radiological assessments were conducted at baseline and during follow-up.
All patients achieved successful outpatient mobilisation [seven patients needed Plerixafor] and underwent transplantation. Median follow-up was 106 weeks (interquartile range [IQR] 52-348). No mobilisation-related serious adverse events [SAEs] or CD worsening occurred. Clinical and endoscopic remission rates were 71% and 41.7% at 26 weeks, 64% and 25% at 52 weeks, and 71% and 16.7% at the last follow-up, respectively. The percentage of patients who restarted CD therapy for clinical relapse and/or endoscopic/radiological activity was 14% at 26 weeks, 57% at 52 weeks, and 86% at the last follow-up, respectively. Peripheral blood cell populations and antibody levels post-AHSCT were comparable to Cy-based mobilisation.
Cy-free mobilisation is safe and feasible in refractory CD patients undergoing AHSCT. Although relapse occurs in a significant proportion of patients, clinical and endoscopic responses are achieved upon CD-specific therapy reintroduction.
自体造血干细胞移植(AHSCT)是治疗难治性克罗恩病(CD)的一种选择。然而,由于化疗毒性和免疫抑制相关的高不良事件发生率,限制了其适用性。本研究旨在评估使用无环磷酰胺(Cy)动员方案的 AHSCT 的安全性和疗效。
本前瞻性观察性研究纳入了 2017 年 6 月至 2022 年 10 月期间进行 AHSCT 的 14 例难治性 CD 患者。方案包括门诊动员,每天给予 G-CSF 12-16μg/kg,连用 5 天,如果 CD34+细胞计数目标未达到,则可选择普乐沙福 240μg/d[1-2 剂]。采用 Cy 和抗胸腺细胞球蛋白标准预处理。在基线和随访期间进行临床、内镜和影像学评估。
所有患者均成功进行门诊动员[7 例患者需要普乐沙福]并接受移植。中位随访时间为 106 周(四分位距 [IQR] 52-348)。无动员相关严重不良事件(SAE)或 CD 恶化发生。26 周时临床和内镜缓解率分别为 71%和 41.7%,52 周时分别为 64%和 25%,末次随访时分别为 71%和 16.7%。因临床复发和/或内镜/影像学活动而重新开始 CD 治疗的患者比例分别为 26 周时 14%,52 周时 57%,末次随访时 86%。AHSCT 后外周血细胞群和抗体水平与基于 Cy 的动员相似。
在进行 AHSCT 的难治性 CD 患者中,无 Cy 动员是安全且可行的。尽管很大一部分患者出现复发,但重新开始 CD 特异性治疗后可获得临床和内镜缓解。