Use of biomarkers in clinical trials and future developments that will help identify novel biomarkers.

ALS (Amyotrophic Lateral Sclerosis) Biomarkers Clinical Outcome Measures Clinical Trials Immunological Mediators Neurofilaments Prognostic Stratification Target Engagement Therapeutic Development Treatment Response

Journal

International review of neurobiology
ISSN: 2162-5514
Titre abrégé: Int Rev Neurobiol
Pays: United States
ID NLM: 0374740

Informations de publication

Date de publication:
2024
Historique:
medline: 28 5 2024
pubmed: 28 5 2024
entrez: 27 5 2024
Statut: ppublish

Résumé

Engineering new solutions for therapeutic benefit in Amyotrophic Lateral Sclerosis (ALS) has proved a difficult task to accomplish. This is largely the reflection of complexities at multiple levels, that require solutions to improve cost-effectiveness and outcomes. The main obstacle related to the condition's clinical heterogeneity, chiefly the broad difference in survival observed among ALS patients, imposes large populations studies and long follow-up to evaluate any efficacy. The emerging solution is composite clinical and biological parameters enabling prognostic stratification into homogeneous phenotypes for more affordable studies. From a therapeutic development perspective, the choice of a medicinal product requires the availability of treatment-specific biomarkers of target engagement to identify off-target effects based on the compound's putative modality of action. More importantly, there are no established biomarkers of treatment response that can complement clinical outcome measures and support futility and end of treatment analyses of efficacy. Ultimately the onus rests on the development of biomarkers encompassing the unmet needs of clinical trial design, from inclusion to efficacy. These readouts of the pathological process may be used in combination with clinical and paraclinical outcome measured, significantly reducing the time and financial burden of clinical studies. Progress towards a biomarker-driven clinical trial design in ALS has been possible thanks to the accurate detection of neurofilaments and of other immunological mediators in biological fluids with the disease progression, a step change enabling the testing of novel therapeutic agents in a new clinical trial setting. However, further progress remains to be made to find treatment specific target engagement biomarkers along with readouts of treatment response that can be reliably applied to all emerging therapies and clinical studies. Here we will cover the basic notions of biomarker development in ALS clinical trials, the most crucial unanswered questions and the unmet needs in the ALS biomarkers space.

Identifiants

pubmed: 38802175
pii: S0074-7742(24)00062-X
doi: 10.1016/bs.irn.2024.04.010
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-207

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Andrea Malaspina (A)

Professor of Neurology, Queen Square MND Centre, Instute of Neurology, London, United Kingdom. Electronic address: a.malaspina@ucl.ac.uk.

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Classifications MeSH