Evaluating the efficacy and safety of transitioning patients with multiple sclerosis from natalizumab to ocrelizumab (OCTAVE).


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
07 2023
Historique:
medline: 12 7 2023
pubmed: 15 6 2023
entrez: 15 6 2023
Statut: ppublish

Résumé

Natalizumab is associated with a risk of progressive multifocal leukoencephalopathy (PML) in multiple sclerosis (MS) patients infected with John Cunningham virus (JCV). Ocrelizumab has demonstrated efficacy to treat MS; however, its safety in patients previously treated with natalizumab is unclear. To evaluate the safety and efficacy of ocrelizumab in patients with relapsing MS (RMS) previously treated with natalizumab. Clinically and radiographically stable RMS patients, ages 18-65 treated with natalizumab for ⩾ 12 months, were enrolled in the study and initiated ocrelizumab 4-6 weeks after their final dose of natalizumab. Relapse assessment, expanded disability status scale, and brain magnetic resonance imaging (MRI) were performed prior to starting ocrelizumab and at months 3, 6, 9, and 12. Forty-three patients were enrolled, and 41 (95%) completed the study. Two patients had a relapse while on ocrelizumab, one at month 9 and the other at month 12, without changes on brain MRI. Two additional patients had new brain MRI lesions detected at month 3, with no new symptoms. Thirteen serious adverse events (SAEs) were recorded, four of which were considered possibly related to ocrelizumab. Overall, our study indicates clinical and MRI stability for most patients transitioning from natalizumab to ocrelizumab. NCT03157830.

Identifiants

pubmed: 37317841
doi: 10.1177/13524585231175284
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Immunologic Factors 0
Natalizumab 0
ocrelizumab A10SJL62JY

Banques de données

ClinicalTrials.gov
['NCT03157830']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

956-966

Auteurs

Kyle Smoot (K)

Providence Brain and Spine Institute, Portland, OR, USA.

Horia Marginean (H)

Providence Brain and Spine Institute, Portland, OR, USA.

Tiffany Gervasi-Follmar (T)

Providence Brain and Spine Institute, Portland, OR, USA.

Chiayi Chen (C)

Providence Brain and Spine Institute, Portland, OR, USA.

Pavle Repovic (P)

Multiple Sclerosis Center, Swedish Neuroscience Institute, Seattle, WA, USA.

Stanley Cohan (S)

Providence Brain and Spine Institute, Portland, OR, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH