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Disease modifying therapy in the treatment of tumefactive multiple sclerosis: A retrospective cohort study.
Galetta, Kristin; Ham, Andrew Siyoon; Vishnevetsky, Anastasia; Bhattacharyya, Shamik; Mateen, Farrah J.
Afiliação
  • Galetta K; Department of Neurology, Stanford University, Palo Alto, CA, USA; Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA. Electronic address: Kgaletta@stanford.edu.
  • Ham AS; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA. Electronic address: Asham@mgh.harvard.edu.
  • Vishnevetsky A; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA. Electronic address: Avishnevetsky@partners.org.
  • Bhattacharyya S; Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA. Electronic address: sbhattacharyya3@bwh.harvard.edu.
  • Mateen FJ; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA. Electronic address: Fmateen@mgh.harvard.edu.
J Neuroimmunol ; 388: 578299, 2024 03 15.
Article em En | MEDLINE | ID: mdl-38364529
ABSTRACT
Tumefactive multiple sclerosis (TMS) is characterized by large demyelinating brain lesions. This was a retrospective cohort study of 67 patients with TMS between January 2015-2023, examining different disease modifying therapy impact on expanded disability scale score change at follow-up. Median age was 36 with a female predominance. Mean EDSS was 3.3 ± 2.3 at TMS onset, 2.1 ± 1.9 at year one, and 2.1 ± 1.9 at last follow-up. A multilinear regression model found higher presentation EDSS and post-diagnosis non-B-cell high efficacy therapies were each independently associated with higher EDSS at last follow up. Further research is needed to determine the value of B-cell therapy in TMS.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Idioma: En Ano de publicação: 2024 Tipo de documento: Article