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Boulanger, Bruno

https://orcid.org/0000-0002-0565-7859

Mayo Clinic

Department of Statistics and Data Science PharmaLex Mont‐Saint‐Guibert Belgium

Citations 2

Debamestrocel multimodal effects on biomarker pathways in amyotrophic lateral sclerosis are linked to clinical outcomes
Lindborg, Stacy , Goyal, Namita , Katz, Jonathan, Burford, Matthew, Li, Jenny, Kaspi, Haggai , Abramov, Natalie, Boulanger, Bruno , Nicholson, Katharine, Mozaffar, Tahseen , Miller, Robert G. , Jenkins, Liberty, Baloh, Robert H. , Lewis, Richard A. , Staff, Nathan P. , Owegi, Margaret, Dagher, Bob, Blondheim-Shraga, N., Gothelf, Yaël, Levy, Yossef S., Kern, R. , Aricha, Revital , Windebank, Anthony J. , Bowser, Robert , Brown, Robert H. , Lindborg, Stacy R , Mozaffar, Tahseen , Lewis, Richard A , Staff, Nathan P , Blondheim-Shraga, Netta R , Bowser, Robert , Cudkowicz, Merit E , Berry, James D. , Cudkowicz, Merit

Muscle & Nerve | April 9, 2024 | Volume: 69 | Issue: 6 | Pages: 719-729

10.1002/mus.28093 Get It

Abstract Introduction/Aims 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. Methods 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. Results 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). Discussion 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.
CSF biomarkers evaluated by principal component analysis in a NurOwn Phase 3 clinical trial (P1-1.Virtual)
Brown, Robert H. , Aricha, Revital , Kern, R. , Windebank, Anthony J. , Goyal, Namita , Katz, Jonathan, Burford, Matthew, Levy, Yossef S., Lebovits, Chaim, Gothelf, Yaël, Boulanger, Bruno , Mehra, Munish, Lindborg, Stacy , Berry, James D. , Cudkowicz, Merit , Staff, Nathan P. , Miller, Robert G. , Mehra, Munish

Neurology | December 6, 2023 | Volume: 98 | Issue: 18_supplement | Pages: No page available

10.1212/wnl.98.18_supplement.2796 Get It