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Effectiveness of autologous haematopoietic stem cell transplantation versus natalizumab in progressive multiple sclerosis.
Kalincik, Tomas; Sharmin, Sifat; Roos, Izanne; Massey, Jennifer; Sutton, Ian; Withers, Barbara; Freedman, Mark S; Atkins, Harold; Krasulova, Eva; Kubala Havrdova, Eva; Trneny, Marek; Kozak, Tomas; Burman, Joachim; Macdonell, Richard; Torkildsen, Øivind; Bø, Lars; Lehmann, Anne Kristine; Sharrack, Basil; Snowden, John.
  • Kalincik T; CORe, Department of Medicine, University of Melbourne, Parkville, Victoria, Australia tomas.kalincik@unimelb.edu.au.
  • Sharmin S; Neuroimmunology Centre, Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Roos I; CORe, Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
  • Massey J; Neuroimmunology Centre, Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Sutton I; CORe, Department of Medicine, University of Melbourne, Parkville, Victoria, Australia.
  • Withers B; Neuroimmunology Centre, Department of Neurology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Freedman MS; Department of Neurology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
  • Atkins H; St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
  • Krasulova E; Department of Neurology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
  • Kubala Havrdova E; University of New South Wales, Sydney, New South Wales, Australia.
  • Trneny M; University of Syndey, Sydney, New South Wales, Australia.
  • Kozak T; St Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia.
  • Burman J; Department of Haematology, St Vincent's Hospital Sydney, Darlinghurst, New South Wales, Australia.
  • Macdonell R; Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Torkildsen Ø; Department of Medicine, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • Bø L; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Lehmann AK; General University Hospital in Prague, Prague, Czech Republic.
  • Sharrack B; Department of Neurology and Center of Clinical Neuroscience, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Snowden J; General University Hospital in Prague, Prague, Czech Republic.
J Neurol Neurosurg Psychiatry ; 95(8): 775-783, 2024 Jul 15.
Article en En | MEDLINE | ID: mdl-38538060
ABSTRACT

BACKGROUND:

Natalizumab was not shown to modify disability in progressive multiple sclerosis (MS). This matched observational study compared the effectiveness of autologous haematopoietic stem cell transplantation (AHSCT) with natalizumab in progressive MS.

METHODS:

Patients with primary/secondary progressive MS from seven AHSCT MS centres and the MSBase registry, treated with AHSCT or natalizumab, were matched on a propensity score derived from sex, age, Expanded Disability Status Scale (EDSS), number of relapses 12/24 months before baseline, time from MS onset, the most effective prior therapy and country. The pairwise-censored groups were compared on hazards of 6-month confirmed EDSS worsening and improvement, relapses and annualised relapse rates (ARRs), using Andersen-Gill proportional hazards models and conditional negative binomial model.

RESULTS:

39 patients treated with AHSCT (37 with secondary progressive MS, mean age 37 years, EDSS 5.7, 28% with recent disability progression, ARR 0.54 during the preceding year) were matched with 65 patients treated with natalizumab. The study found no evidence for difference in hazards of confirmed EDSS worsening (HR 1.49, 95% CI 0.70 to 3.14) and improvement (HR 1.50, 95% CI 0.22 to 10.29) between AHSCT and natalizumab over up to 4 years. The relapse activity was also similar while treated with AHSCT and natalizumab (ARR mean±SD 0.08±0.28 vs 0.08±0.25; HR 1.05, 95% CI 0.39 to 2.82). In the AHSCT group, 3 patients experienced febrile neutropenia during mobilisation, 9 patients experienced serum sickness, 6 patients required intensive care unit admission and 36 patients experienced complications after discharge. No treatment-related deaths were reported.

CONCLUSION:

This study does not support the use of AHSCT to control disability in progressive MS with advanced disability and low relapse activity.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante Autólogo / Trasplante de Células Madre Hematopoyéticas / Esclerosis Múltiple Crónica Progresiva / Natalizumab Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante Autólogo / Trasplante de Células Madre Hematopoyéticas / Esclerosis Múltiple Crónica Progresiva / Natalizumab Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article