Real-World Study of Serum Neurofilament Light Chain Levels in Ocrelizumab-Treated People with Relapsing Multiple Sclerosis

Author:

Barrero Hernández Francisco J.123ORCID,Romero Villarrubia Ana4,Muñoz Fernández Carmen5ORCID,Guillén Martinez Virginia4,Aguilera Del Moral Almudena5,Barrios-López José María4ORCID,Ramírez Rivas Maria A.1,Gálvez Muñoz Antonio J.6ORCID,Piñar Morales Raquel123ORCID

Affiliation:

1. Neurology Unit, University Hospital Clinic San Cecilio, 18016 Granada, Spain

2. Instituto de Investigación Biosanitaria ibs.Granada, 18012 Granada, Spain

3. Departament of Medicine, University of Granada, 18016 Granada, Spain

4. Neurology Unit, University Hospital Virgen de las Nieves, 18014 Granada, Spain

5. Neurology Unit, University Hospital Torrecárdenas, 04009 Almeria, Spain

6. Statistical Advisor and Methodology, Foundation for Biosanitary Research of Eastern Andalusia: FIBAO, 18016 Granada, Spain

Abstract

Serum neurofilament light chain (sNfL) levels have been proposed as a biomarker of the clinical activity, disability progression, and response to treatment of people with multiple sclerosis (PwMS); however, questions remain about its implementation in clinical practice. Ocrelizumab (OCR) has proven effective in improving clinical and radiological outcomes and reducing sNfL levels. This real-life study followed the sNfL levels of 30 PwMS treated for 12 months with OCR and evaluated the usefulness of this biomarker for their short-term prognosis, considering expanded disability status scale (EDSS), annualized relapse rate (ARR), radiological activity, and NEDA-3 values. OCR reduced ARR in 83% of PwMS and radiological activity in 80%. EDSS was maintained, while NEDA-3 was achieved in 70% at 12 months. OCR produced an early reduction in sNfL levels (at 3 months). At baseline, greater MRI-evaluated radiological activity was associated with higher sNfL levels. sNfL levels over the first 12 months of treatment did not predict a suboptimal response or sustained control of the disease. Longer-term studies are needed to explore the predictive usefulness of sNfL levels in PwMS treated with high-efficacy drugs.

Funder

Roche pharma in neuromarker project

Publisher

MDPI AG

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