Biomarker Qualification for Neurofilament Light Chain in Amyotrophic Lateral Sclerosis: Theory and Practice.
Michael BenatarLyle W OstrowJoseph W LewcockFrank BennettJeremy ShefnerRobert BowserPaul LarkinLucie BruijnJoanne WuuPublished in: Annals of neurology (2023)
The increasing incorporation of NfL into ALS therapy development plans provides evidence that its utility-as a prognostic, response, risk/susceptibility, and/or safety biomarker-is already widely accepted by the community. The willingness of the US Food and Drug Administration to base regulatory decisions on rigorous peer-reviewed data-absent formal qualification, leads us to conclude that formal qualification, despite some benefits, is not essential for ongoing and future use of NfL as a tool to aid ALS therapy development. Although the balance of considerations for and against seeking NfL biomarker qualification will undoubtedly vary across different diseases and contexts-of-use, the robustness of the published data and careful deliberations of the ALS community may offer valuable insights for other disease communities grappling with the same issues. ANN NEUROL 2024;95:211-216.
Keyphrases
- mental health
- healthcare
- amyotrophic lateral sclerosis
- drug administration
- electronic health record
- big data
- primary care
- transcription factor
- randomized controlled trial
- cerebrospinal fluid
- stem cells
- systematic review
- current status
- artificial intelligence
- bone marrow
- human health
- meta analyses
- mesenchymal stem cells