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Risk of secondary progression in patients with highly active multiple sclerosis treated with natalizumab: a real-life study.
Scherer, Louisa; Soudant, Marc; Pittion-Vouyovitch, Sophie; Debouverie, Marc; Guillemin, Francis; Epstein, Jonathan; Mathey, Guillaume.
Afiliación
  • Scherer L; Department of Neurology, Nancy University Hospital, 54035, Nancy, France.
  • Soudant M; CIC, Epidémiologie Clinique, CHRU-Nancy, Université de Lorraine, 54000, Nancy, France.
  • Pittion-Vouyovitch S; Department of Neurology, Nancy University Hospital, 54035, Nancy, France.
  • Debouverie M; Department of Neurology, Nancy University Hospital, 54035, Nancy, France.
  • Guillemin F; Université de Lorraine, INSPIIRE, INSERM, 54000, Nancy, France.
  • Epstein J; CIC, Epidémiologie Clinique, CHRU-Nancy, Université de Lorraine, 54000, Nancy, France.
  • Mathey G; Université de Lorraine, INSPIIRE, INSERM, 54000, Nancy, France.
J Neurol ; 271(5): 2216-2224, 2024 May.
Article en En | MEDLINE | ID: mdl-38421420
ABSTRACT

BACKGROUND:

one of the most important therapeutic goals in relapse-onset multiple sclerosis is to preclude conversion to secondary progression. Our objective was to determine the risk of progression associated with natalizumab treatment in an registry-based cohort of patients and to identify determinant factors.

METHODS:

Patients with relapse-onset multiple sclerosis from the Registre Lorrain des Scléroses en Plaques (ReLSEP) were included if they had received one infusion of natalizumab between 2002 and 2021. The risk of secondary progression was determined using a standardized definition and a multi-state estimator to account for the possibility of stopping natalizumab before progression, and analyzed with multivariate Cox models.

RESULTS:

574 patients were followed up for a median of 6.7 years. Of the 304 who stopped NTZ before progression onset, the probabilities (95% confidence interval) to convert to progression after 1, 2, 5 and 10 years were 3.2% (2.0-4.8%), 5.3% (3.6-7.3%), 17.5% (14.3-21.3%) and 28.3% (23.7-33.7%), respectively. Discontinuation of NTZ during follow-up was significantly associated with an increased risk of conversion in case of no resumption of a highly active treatment thereafter (adjusted hazard ratio = 2.7; 95% confidence interval 1.5-4.9; p = 0.001). The use of such a treatment was associated with a lower risk of progression (adjusted hazard ratio = 0.42; 95% confidence interval 0.23-0.79; p = 0.007).

CONCLUSION:

the risk of conversion to secondary progression associated with natalizumab treatment is relatively low but increases in case of natalizumab discontinuation in the absence of switch to highly active immunosuppressant.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sistema de Registros / Progresión de la Enfermedad / Natalizumab / Factores Inmunológicos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sistema de Registros / Progresión de la Enfermedad / Natalizumab / Factores Inmunológicos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: J Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia