Alemtuzumab following natalizumab is more effective in adult-onset than paediatric-onset multiple sclerosis

Author:

Puthenparampil Marco12ORCID,Gaggiola Marta32,Miscioscia Alessandro34,Mauceri Valentina Annamaria32,De Napoli Federica32,Zanotelli Giovanni32,Anglani Mariagiulia5,Nosadini Margherita67,Sartori Stefano67,Perini Paola2,Rinaldi Francesca2,Gallo Paolo32

Affiliation:

1. Multiple Sclerosis Centre, Clinica Neurologica, Dipartimento di Neuroscienze, Università degli Studi di Padova, Via Giustiniani 5, 35128 Padova, Italy

2. Multiple Sclerosis Centre, Azienda Ospedaliera di Padova, Padova, Italy

3. Department of Neurosciences, University of Padua, Padova, Italy

4. Padua Neuroscience Centre, University of Padua, Padova, Italy

5. Neuroradiology Unit, Azienda Ospedaliera di Padova, Padova, Italy

6. Paediatric Neurology and Neurophysiology Unit, Department of Women’s and Children’s Health, University Hospital of Padova, Padova, Italy

7. Neuroimmunology Group, Paediatric Research Institute ‘Città della Speranza’, Padova, Italy

Abstract

Background: Paediatric-onset multiple sclerosis (POMS) therapeutic approach derives from of adult-onset multiple sclerosis (AOMS) tailored algorithms. Objectives: To evaluate in a common clinical scenario the efficacy and safety of alemtuzumab (ALZ) in POMS and AOMS. Methods: All patients switching from natalizumab (NTZ) to ALZ for safety concerns (high anti-John Cunningham Virus Antibody Index value, anti-JCV Index) were enrolled in this single-centre, retrospective, case-control open-label study. Results: Ten POMS and 27 AOMS were followed up for 51.3 months. After month 12, we found a lower risk of clinical or radiological relapses among AOMS patients and among patients with older age at ALZ (both p < 0.05). Survival analysis revealed an increased risk of relapse in POMS compared with AOMS (logrank p = 0.00498) and patients starting ALZ before age 22.75 years than the elder ones (logrank p = 0.0018). Survival analysis did not disclose any difference between AOMS and POMS (logrank p = 0.27) in terms of progression independent of any relapse activity (PIRA). In addition, no evidence of relapse-associated worsening was observed. Autoimmune events were reported by 5 AOMS and no POMS (29.4% versus 0.0%, p = 0.057), and survival analysis was not significant (logrank p = 0.0786). Conclusion: ALZ seems more effective in AOMS than in POMS following NTZ. These findings underrate ALZ effectiveness when shifting from NTZ in POMS.

Funder

Biogen Italia Srl

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology,Pharmacology

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