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环磷酰胺免预处理动员方案增加了难治性克罗恩病患者自体造血干细胞移植的安全性和疗效。

Cyclophosphamide-free Mobilisation Increases Safety While Preserving the Efficacy of Autologous Haematopoietic Stem Cell Transplantation in Refractory Crohn's Disease Patients.

机构信息

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.

出版信息

J Crohns Colitis. 2024 Oct 15;18(10):1701-1712. doi: 10.1093/ecco-jcc/jjae076.

Abstract

BACKGROUND AND AIM

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景与目的

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。

方法

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。

结果

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。

结论

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。

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