Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation

BackgroundBehçet’s Disease (BD) is an autoimmune disease mostly presenting with recurrent oral and genital aphthosis, and uveitis. Patients are rarely refractory to immunosuppressive treatments. Autologous hematopoietic stem cell transplantation (aHSCT) is a standard of care in other autoimmune dise...

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Main Authors: Mathieu Puyade, Amit Patel, Yeong Jer Lim, Norbert Blank, Manuela Badoglio, Francesca Gualandi, David D. Ma, Natalia Maximova, Raffaella Greco, Tobias Alexander, John A. Snowden
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2021.638709/full
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spelling doaj-497228ed6628488181a5e71f656c9e262021-05-06T05:10:08ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-05-011210.3389/fimmu.2021.638709638709Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow TransplantationMathieu Puyade0Mathieu Puyade1Amit Patel2Yeong Jer Lim3Norbert Blank4Manuela Badoglio5Francesca Gualandi6David D. Ma7Natalia Maximova8Raffaella Greco9Raffaella Greco10Tobias Alexander11Tobias Alexander12John A. Snowden13CHU de Poitiers, Service de Médecine Interne et Maladies Infectieuses, Poitiers, FranceCHU de Poitiers, CIC-1402 Poitiers, FranceHaematology and Transplant Unit, The Christie NHS Foundation Trust, Manchester, United KingdomHaemato-Oncology Department, Clatterbridge Cancer Centre, University of Liverpool, Liverpool, United KingdomDepartment of Hematology, Oncology and Rheumatology, Internal Medicine V, University Hospital of Heidelberg, Heidelberg, GermanyEBMT ADWP Office, Paris, FranceU.O. Ematologia Centro Trapianti Midollo - Ospedale Policlinico San Martino, Genova, ItalyDepartment of Haematology and BM Transplantation, St Vincent’s Hospital Sydney and St Vincent’s Clinical School, Faculty of Medicine, University of New South Wales (UNSW) Sydney, Sydney, NSW, AustraliaInstitute for Maternal and Child Health – IRCCS Burlo Garofolo, Trieste, Italy0Haematology and Bone Marrow Transplant Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy1Vita-Salute San Raffaele University, Milan, Italy2Department of Rheumatology and Clinical Immunology, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Charité - Universitätsmedizin Berlin, Berlin, Germany3Deutsches Rheuma-Forschungszentrum (DRFZ), an Institute of the Leibniz Association, Berlin, Germany4Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United KingdomBackgroundBehçet’s Disease (BD) is an autoimmune disease mostly presenting with recurrent oral and genital aphthosis, and uveitis. Patients are rarely refractory to immunosuppressive treatments. Autologous hematopoietic stem cell transplantation (aHSCT) is a standard of care in other autoimmune diseases. Some patients with BD have been treated with aHSCT based on compassionate use.ObjectivesEvaluate the outcome of aHSCT in adult patients with BD treated in member centers of the European Society for Blood and Marrow Transplantation (EBMT).MethodsAdults who received aHSCT primarily for BD were identified retrospectively in the EBMT registry and/or in published literature. Data were extracted from either medical records of the patient or from publications.ResultsEight out of 9 cases reported to the registry and extracted data of 2 further patients from literature were analyzed. Four were female, median age at onset of BD was 24y (range 9-50). Median age at aHSCT was 32y (27-51). Patients had received median 4 (2-11) previous lines of therapy (89% corticosteroids, 50% methotrexate, anti-TNFα therapy or cyclophosphamide). All patients had active disease before mobilization. Conditioning regimen was heterogeneous. Median follow-up was 48 months (range 6-240). No treatment-related mortality was reported. This procedure induced complete remission (CR) in 80%, partial remission in 10% and lack of response in 10% of the patients. Relapse rate was 30% (2 relapses in patients in CR and 1 relapse in the patient in PR) with panuveitis (n=1), aphthosis (n=2) and arthralgia (n=1). Six patients were in CR. No late complications were reported.ConclusionaHSCT has an acceptable safety profile and represents a feasible and relatively effective procedure in severe and conventional treatment-resistant cases of BD and has the potential to stabilize BD in patients with life-threatening involvements.https://www.frontiersin.org/articles/10.3389/fimmu.2021.638709/fullBehçet’s diseaseautologous stem cell transplantationefficacytoxicityimmune reset
collection DOAJ
language English
format Article
sources DOAJ
author Mathieu Puyade
Mathieu Puyade
Amit Patel
Yeong Jer Lim
Norbert Blank
Manuela Badoglio
Francesca Gualandi
David D. Ma
Natalia Maximova
Raffaella Greco
Raffaella Greco
Tobias Alexander
Tobias Alexander
John A. Snowden
spellingShingle Mathieu Puyade
Mathieu Puyade
Amit Patel
Yeong Jer Lim
Norbert Blank
Manuela Badoglio
Francesca Gualandi
David D. Ma
Natalia Maximova
Raffaella Greco
Raffaella Greco
Tobias Alexander
Tobias Alexander
John A. Snowden
Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
Frontiers in Immunology
Behçet’s disease
autologous stem cell transplantation
efficacy
toxicity
immune reset
author_facet Mathieu Puyade
Mathieu Puyade
Amit Patel
Yeong Jer Lim
Norbert Blank
Manuela Badoglio
Francesca Gualandi
David D. Ma
Natalia Maximova
Raffaella Greco
Raffaella Greco
Tobias Alexander
Tobias Alexander
John A. Snowden
author_sort Mathieu Puyade
title Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
title_short Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
title_full Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
title_fullStr Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
title_full_unstemmed Autologous Hematopoietic Stem Cell Transplantation for Behçet’s Disease: A Retrospective Survey of Patients Treated in Europe, on Behalf of the Autoimmune Diseases Working Party of the European Society for Blood and Marrow Transplantation
title_sort autologous hematopoietic stem cell transplantation for behçet’s disease: a retrospective survey of patients treated in europe, on behalf of the autoimmune diseases working party of the european society for blood and marrow transplantation
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-05-01
description BackgroundBehçet’s Disease (BD) is an autoimmune disease mostly presenting with recurrent oral and genital aphthosis, and uveitis. Patients are rarely refractory to immunosuppressive treatments. Autologous hematopoietic stem cell transplantation (aHSCT) is a standard of care in other autoimmune diseases. Some patients with BD have been treated with aHSCT based on compassionate use.ObjectivesEvaluate the outcome of aHSCT in adult patients with BD treated in member centers of the European Society for Blood and Marrow Transplantation (EBMT).MethodsAdults who received aHSCT primarily for BD were identified retrospectively in the EBMT registry and/or in published literature. Data were extracted from either medical records of the patient or from publications.ResultsEight out of 9 cases reported to the registry and extracted data of 2 further patients from literature were analyzed. Four were female, median age at onset of BD was 24y (range 9-50). Median age at aHSCT was 32y (27-51). Patients had received median 4 (2-11) previous lines of therapy (89% corticosteroids, 50% methotrexate, anti-TNFα therapy or cyclophosphamide). All patients had active disease before mobilization. Conditioning regimen was heterogeneous. Median follow-up was 48 months (range 6-240). No treatment-related mortality was reported. This procedure induced complete remission (CR) in 80%, partial remission in 10% and lack of response in 10% of the patients. Relapse rate was 30% (2 relapses in patients in CR and 1 relapse in the patient in PR) with panuveitis (n=1), aphthosis (n=2) and arthralgia (n=1). Six patients were in CR. No late complications were reported.ConclusionaHSCT has an acceptable safety profile and represents a feasible and relatively effective procedure in severe and conventional treatment-resistant cases of BD and has the potential to stabilize BD in patients with life-threatening involvements.
topic Behçet’s disease
autologous stem cell transplantation
efficacy
toxicity
immune reset
url https://www.frontiersin.org/articles/10.3389/fimmu.2021.638709/full
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