Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/216580
Title: Cyclophosphamide-free Mobilisation Increases Safety While Preserving the Efficacy of Autologous Haematopoietic Stem Cell Transplantation in Refractory Crohn's Disease Patients
Author: Giordano, Antonio
Rovira Tarrats, Montserrat
Veny Álvarez-Ossorio, Marisol
Barastegui Baget, Rebeca
Marín Fernández, Pedro José
Martínez Muñoz, Ma. Carmen
Fernández Avilés, F.
Suarez Lledó Grande, María
Domenech, Ariadna
Serrahima, Anna
Lozano Molero, Miguel
Cid Vidal, Joan
Ordas Jimenez, Ingrid
Fernández Clotet, Agnès
Caballol Oliva, Berta
Gallego Barrero, Marta
Vara, Alejandro
Masamunt, Maria Carme
Giner Agudo, Àngel
Teubel, Iris
Esteller Viñal, Miriam
Corraliza Márquez, Ana Maria
Panés Díaz, Julià
Salas Martínez, Maria Azucena
Ricart, Elena (Ricart Gómez)
Keywords: Malaltia de Crohn
Autotrasplantament
Ciclofosfamida
Crohn's disease
Autotransplantation
Cyclophosphamide
Issue Date: 5-Jun-2024
Publisher: Oxford University Press
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 mu g/kg/daily for 5 days, and optional Plerixafor 240 mu g/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. Graphical Abstract
Note: Versió postprint del document publicat a: https://doi.org/10.1093/ecco-jcc/jjae076
It is part of: Journal Of Crohns & Colitis, 2024, vol. 18, num. 10, p.1701-1712
URI: https://hdl.handle.net/2445/216580
Related resource: https://doi.org/10.1093/ecco-jcc/jjae076
ISSN: 1876-4479
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)



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