Clinical validation of a novel in vitro diagnostic neurofilament light chain assay for the prognostication of disease activity in people with relapsing multiple sclerosis

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

  • Tjalf Ziemssen - , Department of Neurology (Author)
  • Mark S Freedman - , Ottawa Hospital Research Institute (Author)
  • Amit Bar-Or - , University of Pennsylvania Perelman School of Medicine (Author)
  • Xavier Montalban - , Vall d'Hebron University Hospital , Autonomous University of Barcelona, The University of Vic - Central University of Catalonia (Author)
  • Charlotte E Teunissen - , Amsterdam University Medical Centers (UMC) (Author)
  • Dieter A Häring - , Novartis AG (Author)
  • Petra Kukkaro - , Novartis AG (Author)
  • Martin Merschhemke - , Novartis AG (Author)
  • Bernd C Kieseier - , Novartis AG (Author)
  • Meghana Karnik-Henry - , Siemens Healthineers (Author)
  • Matthew Gee - , Siemens Healthineers (Author)
  • Sascha Lange - , Siemens Healthineers (Author)
  • Eddine Merabet - , Siemens Healthineers (Author)
  • Tanuja Chitnis - , Brigham and Women's Hospital, Harvard Medical School (HMS) (Author)
  • Stefan Bittner - , University Medical Center Mainz (Author)
  • Heinz Wiendl - , University Medical Center Freiburg (Author)
  • Stephen L Hauser - , UCSF Weill Institute for Neuroscience (Author)

Abstract

BACKGROUND: Neurofilament light chain (NfL) is a promising marker for predicting disease activity in relapsing multiple sclerosis (RMS). To date, however, there has been no commercially available NfL assay validated in MS and intended for routine clinical use.

OBJECTIVE: To identify and validate a single threshold for NfL in blood that differentiates RMS patients, aged 18-55 years, at a higher versus lower risk of disease activity over 2 years, using the Atellica® IM NfL assay.

METHODS: The optimal NfL threshold for this assay/use case was identified and independently validated using ASCLEPIOS I and II data, respectively. The primary endpoint (annualized number of new/enlarging T2 (neT2) lesions) was analyzed using negative binomial models. Threshold optimization used maximum likelihood methodology. Generalizability analyses used data from ASCLEPIOS II, FREEDOMS, and TRANSFORMS.

RESULTS: NfL concentration of 12.9 pg/mL was validated as the optimal cutoff for prognosticating disease activity as measured by neT2 lesion over 2 years. This threshold prognosticated individual patient risk for persistent disease activity (>3 neT2 lesions/year over 2 years) and showed prognostic value across relevant subgroups and clinical scenarios. Findings for relapses were similar.

CONCLUSION: The CE-marked Atellica® IM NfL assay is now validated for prognostic use in RMS patients.

Details

Original languageEnglish
Pages (from-to)1543-1556
Number of pages14
JournalMultiple Sclerosis Journal
Volume31
Issue number13
Early online date29 Oct 2025
Publication statusPublished - Nov 2025
Peer-reviewedYes

External IDs

ORCID /0000-0001-8799-8202/work/196056207
Scopus 105020451338

Keywords