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Escalating to medium- versus high-efficacy disease modifying therapy after low-efficacy treatment in relapsing remitting multiple sclerosis.
Müller, Jannis; Roos, Izanne; Kalincik, Tomas; Lorscheider, Johannes; Galli, Edoardo; Benkert, Pascal; Schädelin, Sabine; Sharmin, Sifat; Einsiedler, Maximilian; Hänni, Peter; Schmid, Jürg; Kuhle, Jens; Derfuss, Tobias; Granziera, Cristina; Ziemssen, Tjalf; Siepmann, Timo; Yaldizli, Özgür.
Afiliación
  • Müller J; Neurology Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, MS Center and Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University o
  • Roos I; Division of Health Care Sciences, Dresden International University, Dresden, Germany.
  • Kalincik T; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Lorscheider J; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Galli E; Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia.
  • Benkert P; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Schädelin S; Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia.
  • Sharmin S; Neurology Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, MS Center and Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University o
  • Einsiedler M; Neurology Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, MS Center and Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University o
  • Hänni P; Department of Clinical Research, Clinical Trial Unit, University Hospital Basel, Basel, Switzerland.
  • Schmid J; Department of Clinical Research, Clinical Trial Unit, University Hospital Basel, Basel, Switzerland.
  • Kuhle J; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Derfuss T; Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia.
  • Granziera C; Neurology Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, MS Center and Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University o
  • Ziemssen T; Swiss Federation for Common Tasks of Health Insurances (SVK), Solothurn, Switzerland.
  • Siepmann T; Swiss Federation for Common Tasks of Health Insurances (SVK), Solothurn, Switzerland.
  • Yaldizli Ö; Neurology Clinic and Policlinic, Departments of Head, Spine and Neuromedicine, MS Center and Translational Imaging in Neurology (ThINk) Basel, Department of Biomedical Engineering, Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University o
Brain Behav ; 14(5): e3498, 2024 May.
Article en En | MEDLINE | ID: mdl-38688877
ABSTRACT

BACKGROUND:

In patients with relapsing remitting multiple sclerosis (RRMS) on low-efficacy disease modifying therapies (DMT), the optimal strategy on how to escalate treatment once needed, remains unknown.

METHODS:

We studied RRMS patients on low-efficacy DMTs listed in the Swiss National Treatment Registry, who underwent escalation to either medium- or high-efficacy DMTs. Propensity score-based matching was applied using 12 clinically relevant variables. Both groups were also separately matched with control subjects who did not escalate therapy. Time to relapse and to disability worsening were evaluated using Cox proportional hazard models.

RESULTS:

Of 1037 eligible patients, we 11 matched 450 MS patients who switched from low-efficacy to medium-efficacy (n = 225; 76.0% females, aged 42.4 ± 9.9 years [mean ± SD], median EDSS 3.0 [IQR 2-4]) or high-efficacy DMTs (n = 225; 72.4% females, aged 42.2 ± 10.6 years, median EDSS 3.0 [IQR 2-4]). Escalation to high-efficacy DMTs was associated with lower hazards of relapses than medium-efficacy DMTs (HR = 0.67, 95% CI 0.47-0.95, p = .027) or control subjects (HR = 0.61, 95% CI 0.44-0.84, p = .003). By contrast, escalation from low to medium-efficacy DMTs did not alter the hazard for relapses when compared to controls (i.e. patients on low-efficacy DMT who did not escalate DMT during follow-up)

CONCLUSION:

Our nationwide registry analysis suggests that, once escalation from a low-efficacy DMT is indicated, switching directly to a high-efficacy treatment is superior to a stepwise escalation starting with a moderate-efficacy treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Brain Behav Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Esclerosis Múltiple Recurrente-Remitente Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Brain Behav Año: 2024 Tipo del documento: Article