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      Haematopoietic SCT in severe autoimmune diseases: updated guidelines of the European Group for Blood and Marrow Transplantation

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          Abstract

          In 1997, the first consensus guidelines for haematopoietic SCT (HSCT) in autoimmune diseases (ADs) were published, while an international coordinated clinical programme was launched. These guidelines provided broad principles for the field over the following decade and were accompanied by comprehensive data collection in the European Group for Blood and Marrow Transplantation (EBMT) AD Registry. Subsequently, retrospective analyses and prospective phase I/II studies generated evidence to support the feasibility, safety and efficacy of HSCT in several types of severe, treatment-resistant ADs, which became the basis for larger-scale phase II and III studies. In parallel, there has also been an era of immense progress in biological therapy in ADs. The aim of this document is to provide revised and updated guidelines for both the current application and future development of HSCT in ADs in relation to the benefits, risks and health economic considerations of other modern treatments. Patient safety considerations are central to guidance on patient selection and HSCT procedural aspects within appropriately experienced and Joint Accreditation Committee of International Society for Cellular Therapy and EBMT accredited centres. A need for prospective interventional and non-interventional studies, where feasible, along with systematic data reporting, in accordance with EBMT policies and procedures, is emphasized.

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          Most cited references171

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          International consensus report on the investigation and management of primary immune thrombocytopenia.

          Previously published guidelines for the diagnosis and management of primary immune thrombocytopenia (ITP) require updating largely due to the introduction of new classes of therapeutic agents, and a greater understanding of the disease pathophysiology. However, treatment-related decisions still remain principally dependent on clinical expertise or patient preference rather than high-quality clinical trial evidence. This consensus document aims to report on new data and provide consensus-based recommendations relating to diagnosis and treatment of ITP in adults, in children, and during pregnancy. The inclusion of summary tables within this document, supported by information tables in the online appendices, is intended to aid in clinical decision making.
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              Immunosuppressive therapy in lupus nephritis: the Euro-Lupus Nephritis Trial, a randomized trial of low-dose versus high-dose intravenous cyclophosphamide.

              Glomerulonephritis is a severe manifestation of systemic lupus erythematosus (SLE) that is usually treated with an extended course of intravenous (IV) cyclophosphamide (CYC). Given the side effects of this regimen, we evaluated the efficacy and the toxicity of a course of low-dose IV CYC prescribed as a remission-inducing treatment, followed by azathioprine (AZA) as a remission-maintaining treatment. In this multicenter, prospective clinical trial (the Euro-Lupus Nephritis Trial [ELNT]), we randomly assigned 90 SLE patients with proliferative glomerulonephritis to a high-dose IV CYC regimen (6 monthly pulses and 2 quarterly pulses; doses increased according to the white blood cell count nadir) or a low-dose IV CYC regimen (6 fortnightly pulses at a fixed dose of 500 mg), each of which was followed by AZA. Intent-to-treat analyses were performed. Followup continued for a median of 41.3 months in the low-dose group and 41 months in the high-dose group. Sixteen percent of those in the low-dose group and 20% of those in the high-dose group experienced treatment failure (not statistically significant by Kaplan-Meier analysis). Levels of serum creatinine, albumin, C3, 24-hour urinary protein, and the disease activity scores significantly improved in both groups during the first year of followup. Renal remission was achieved in 71% of the low-dose group and 54% of the high-dose group (not statistically significant). Renal flares were noted in 27% of the low-dose group and 29% of the high-dose group. Although episodes of severe infection were more than twice as frequent in the high-dose group, the difference was not statistically significant. The data from the ELNT indicate that in European SLE patients with proliferative lupus nephritis, a remission-inducing regimen of low-dose IV CYC (cumulative dose 3 gm) followed by AZA achieves clinical results comparable to those obtained with a high-dose regimen.
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                Author and article information

                Journal
                Bone Marrow Transplant
                Bone Marrow Transplant
                Bone Marrow Transplantation
                Nature Publishing Group
                0268-3369
                1476-5365
                June 2012
                17 October 2011
                : 47
                : 6
                : 770-790
                Affiliations
                [1 ]simpleDepartment of Haematology, Sheffield Teaching Hospitals NHS Trust , Sheffield, UK
                [2 ]simpleDepartment of Oncology, University of Sheffield , Sheffield, UK
                [3 ]simpleDepartment of Haematology, Careggi University Hospital , Firenze, Italy
                [4 ]simpleService de Gastroentérologie, INSERM U 662, Hôpital St Louis , Paris, France
                [5 ]simpleDepartment of Gastroenterology, Sacco University Hospital , Milan, Italy
                [6 ]simpleCharite Hospital Berlin , Berlin, Germany
                [7 ]simpleDepartment of Autoimmune Diseases, Hospital Clinic , Barcelona, Spain
                [8 ]simpleCentre for Rheumatology, Royal Free and University College Medical School , Hampstead, London, UK
                [9 ]simpleNottingham Digestive Diseases Centre, University of Nottingham , Nottingham, UK
                [10 ]simpleHôpital Saint Antoine, Service d'Hématologie et Thérapie Cellulaire, AP-HP, UPMC Univ Paris 06 , Paris, France
                [11 ]simpleDepartment of Neuroscience, Ophthalmology and Genetics, University of Genova , Genova, Italy
                [12 ]simpleInstitute for Neuroimmunology and Clinical MS Research , Hamburg, Germany
                [13 ]simpleSt Vincent's Hospital , Sydney, NSW, Australia
                [14 ]simpleUniversitaetsspital Basel , Basel, Switzerland
                [15 ]simpleBMT Unit, St Anna Children's Hospital , Vienna, Austria
                [16 ]simpleBMT Unit, Department of Pediatrics, Institute of Maternal and Child Health Burlo Garofolo , Trieste, Italy
                [17 ]simpleSCT Unit, Hematology Department, Hospital Clinic , Barcelona, Spain
                [18 ]simpleNewcastle University , Newcastle-Upon-Tyne, UK
                [19 ]simpleDepartment of Internal Medicine, INSERM U 796, Hôpital St Louis , Paris, France
                Author notes
                [* ]simpleDepartment of Haematology, Sheffield Teaching Hospitals NHS Trust, University of Sheffield , Glossop Road, Sheffield S10 2JF, UK. E-mail: john.snowden@ 123456sth.nhs.uk
                [* ]simpleEBMT Autoimmune Diseases Working Party (ADWP), EBMT Paris Office , Paris, France. E-mail: dominique.farge-bancel@ 123456sls.aphp.fr
                [20]

                Representative of the Bone Marrow Transplantation Society of Australia and New Zealand (BMTSANZ).

                [21]

                Representative of the EBMT Paediatric Diseases Working Party (PDWP).

                Article
                bmt2011185
                10.1038/bmt.2011.185
                3371413
                22002489
                9f3c5d36-f20d-4692-88ad-c69f9805f9e8
                Copyright © 2012 Macmillan Publishers Limited

                This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 03 May 2011
                : 04 July 2011
                : 04 July 2011
                Categories
                Special Report

                Transplantation
                guidelines,autoimmune diseases,recommendations,haematopoietic sct,autologous,allogeneic

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