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

dc.contributor.author
Giordano, Antonio
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Rovira Tarrats, Montserrat
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Veny Álvarez-Ossorio, Marisol
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Barastegui Baget, Rebeca
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Marín Fernández, Pedro José
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Martínez Muñoz, Ma. Carmen
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Fernández Avilés, F.
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Suárez-Lledó Grande, María
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Domenech, Ariadna
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Serrahima, Anna
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Lozano Molero, Miguel
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Cid Vidal, Joan
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Ordas Jimenez, Ingrid
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Fernández Clotet, Agnès
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Caballol Oliva, Berta
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Gallego Barrero, Marta
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Vara, Alejandro
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Masamunt, Maria Carme
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Giner Agudo, Àngel
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Teubel, Iris
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Esteller Viñal, Miriam
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Corraliza Márquez, Ana Maria
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Panés Díaz, Julià
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Salas Martínez, Azucena
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Ricart, Elena (Ricart Gómez)
dc.date.issued
2024-11-18T18:50:34Z
dc.date.issued
2025-06-05T05:10:09Z
dc.date.issued
2024-06-05
dc.date.issued
2024-11-15T11:34:06Z
dc.identifier
1876-4479
dc.identifier
https://hdl.handle.net/2445/216580
dc.identifier
9428813
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38757210
dc.description.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
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45 p.
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application/pdf
dc.language
eng
dc.publisher
Oxford University Press
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1093/ecco-jcc/jjae076
dc.relation
Journal Of Crohns & Colitis, 2024, vol. 18, num. 10, p.1701-1712
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https://doi.org/10.1093/ecco-jcc/jjae076
dc.rights
(c) Giordano, Antonio et al., 2024
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject
Malaltia de Crohn
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Autotrasplantament
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Ciclofosfamida
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Crohn's disease
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Autotransplantation
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Cyclophosphamide
dc.title
Cyclophosphamide-free Mobilisation Increases Safety While Preserving the Efficacy of Autologous Haematopoietic Stem Cell Transplantation in Refractory Crohn's Disease Patients
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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