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Autologous hematopoietic stem cell transplantation in neuromyelitis optica : A registry study of the EBMT Autoimmune Diseases Working Party

Authors :
Greco, Raffaella
Bondanza, Attilio
Oliveira, Maria Carolina
Badoglio, Manuela
Burman, Joachim
Piehl, Fredrik
Hägglund, Hans
Krasulova, Eva
Simões, Belinda Pinto
Carlson, Kristina
Pohlreich, David
Labopin, Myriam
Saccardi, Riccardo
Comi, Giancarlo
Mancardi, Gian Luigi
Bacigalupo, Andrea
Ciceri, Fabio
Farge, Dominique
Greco, Raffaella
Bondanza, Attilio
Oliveira, Maria Carolina
Badoglio, Manuela
Burman, Joachim
Piehl, Fredrik
Hägglund, Hans
Krasulova, Eva
Simões, Belinda Pinto
Carlson, Kristina
Pohlreich, David
Labopin, Myriam
Saccardi, Riccardo
Comi, Giancarlo
Mancardi, Gian Luigi
Bacigalupo, Andrea
Ciceri, Fabio
Farge, Dominique
Publication Year :
2015

Abstract

BACKGROUND: Neuromyelitis optica (NMO) is an inflammatory autoimmune disorder of the central nervous system, hallmarked by pathogenic anti-aquaporin 4 antibodies. NMO prognosis is worse compared with multiple sclerosis. OBJECTIVE: The European Group for Blood and Marrow Transplantation (EBMT) Autoimmune Diseases Working Party (ADWP) conducted a retrospective survey to analyze disease outcome following autologous stem cell transplantation (ASCT). METHODS: This retrospective multicenter study assessed the efficacy and safety of ASCT in 16 patients suffering from refractory NMO reported to the EBMT registry between 2001 and 2011. RESULTS: Fifteen patients were successfully mobilized with cyclophosphamide (Cy) and G-CSF, one with G-CSF alone. All patients received an unmanipulated autologous peripheral blood stem cell graft, after conditioning with BEAM plus anti-thymocyte globulin (ATG, n = 9 patients), thiotepa-Cy (n = 3) or Cy (200 mg/kg) plus ATG (n = 4). After a median follow-up of 47 months, three of 16 cases were progression and treatment free, while in the remaining 13 patients further treatments were administered for disability progression or relapse after ASCT. Altogether, relapse-free survival at three and five years was 31% and 10%, respectively, while progression-free survival remained 48% at three and five years. CONCLUSIONS: In these NMO patients, highly resistant to conventional treatment, ASCT allows for temporary control of the disease, despite a tendency to progress or relapse in the long term.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1235139070
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1177.1352458514541978