Debamestrocel multimodal effects on biomarker pathways in amyotrophic lateral sclerosis are linked to clinical outcomes.

amyotrophic lateral sclerosis biomarker cellular therapy

Journal

Muscle & nerve
ISSN: 1097-4598
Titre abrégé: Muscle Nerve
Pays: United States
ID NLM: 7803146

Informations de publication

Date de publication:
09 Apr 2024
Historique:
revised: 16 03 2024
received: 01 09 2023
accepted: 19 03 2024
medline: 10 4 2024
pubmed: 10 4 2024
entrez: 9 4 2024
Statut: aheadofprint

Résumé

Biomarkers have shown promise in amyotrophic lateral sclerosis (ALS) research, but the quest for reliable biomarkers remains active. This study evaluates the effect of debamestrocel on cerebrospinal fluid (CSF) biomarkers, an exploratory endpoint. A total of 196 participants randomly received debamestrocel or placebo. Seven CSF samples were to be collected from all participants. Forty-five biomarkers were analyzed in the overall study and by two subgroups characterized by the ALS Functional Rating Scale-Revised (ALSFRS-R). A prespecified model was employed to predict clinical outcomes leveraging biomarkers and disease characteristics. Causal inference was used to analyze relationships between neurofilament light chain (NfL) and ALSFRS-R. We observed significant changes with debamestrocel in 64% of the biomarkers studied, spanning pathways implicated in ALS pathology (63% neuroinflammation, 50% neurodegeneration, and 89% neuroprotection). Biomarker changes with debamestrocel show biological activity in trial participants, including those with advanced ALS. CSF biomarkers were predictive of clinical outcomes in debamestrocel-treated participants (baseline NfL, baseline latency-associated peptide/transforming growth factor beta1 [LAP/TGFβ1], change galectin-1, all p < .01), with baseline NfL and LAP/TGFβ1 remaining (p < .05) when disease characteristics (p < .005) were incorporated. Change from baseline to the last measurement showed debamestrocel-driven reductions in NfL were associated with less decline in ALSFRS-R. Debamestrocel significantly reduced NfL from baseline compared with placebo (11% vs. 1.6%, p = .037). Following debamestrocel treatment, many biomarkers showed increases (anti-inflammatory/neuroprotective) or decreases (inflammatory/neurodegenerative) suggesting a possible treatment effect. Neuroinflammatory and neuroprotective biomarkers were predictive of clinical response, suggesting a potential multimodal mechanism of action. These results offer preliminary insights that need to be confirmed.

Identifiants

pubmed: 38593477
doi: 10.1002/mus.28093
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : California Institute for Regenerative Medicine
Organisme : I AM ALS
Organisme : ALS Association

Informations de copyright

Muscle & Nerve© 2024 The Authors. Muscle & Nerve published by Wiley Periodicals LLC.

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Auteurs

Stacy R Lindborg (SR)

Brainstorm Cell Therapeutics, Boston, Massachusetts, USA.

Namita A Goyal (NA)

UCI Health ALS & Neuromuscular Center, University of California, Irvine, California, USA.

Jonathan Katz (J)

Sutter Pacific Medical Foundation, California Pacific Medical Center, San Francisco, California, USA.

Matthew Burford (M)

Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Jenny Li (J)

Brainstorm Cell Therapeutics, Boston, Massachusetts, USA.

Haggai Kaspi (H)

Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Natalie Abramov (N)

Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Bruno Boulanger (B)

Department of Statistics and Data Science, PharmaLex, Mont-Saint-Guibert, Belgium.

James D Berry (JD)

Healey & AMG Center, Mass General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Katharine Nicholson (K)

Healey & AMG Center, Mass General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Tahseen Mozaffar (T)

UCI Health ALS & Neuromuscular Center, University of California, Irvine, California, USA.

Robert Miller (R)

Sutter Pacific Medical Foundation, California Pacific Medical Center, San Francisco, California, USA.

Liberty Jenkins (L)

Sutter Pacific Medical Foundation, California Pacific Medical Center, San Francisco, California, USA.

Robert H Baloh (RH)

Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Richard Lewis (R)

Department of Neurology, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Nathan P Staff (NP)

Department of Neurology, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

Margaret Ayo Owegi (MA)

Neurology Department, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Bob Dagher (B)

Brainstorm Cell Therapeutics, Boston, Massachusetts, USA.

Netta R Blondheim-Shraga (NR)

Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Yael Gothelf (Y)

Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Yossef S Levy (YS)

Manufacturing, Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Ralph Kern (R)

Brainstorm Cell Therapeutics, Boston, Massachusetts, USA.

Revital Aricha (R)

Brainstorm Cell Therapeutics, Tel Aviv, Israel.

Anthony J Windebank (AJ)

Department of Neurology, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

Robert Bowser (R)

Department of Neurology, Barrow Neurological Institute, Phoenix, Arizona, USA.

Robert H Brown (RH)

Neurology Department, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Merit E Cudkowicz (ME)

Healey & AMG Center, Mass General Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Classifications MeSH