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  • Improved Clinical and MRI Disease Activity Outcomes, Including Slowing of Brain Volume Loss, in Alemtuzumab-Treated RRMS Patients: 8-Year Follow-up of CARE-MS II (TOPAZ Study)

    Author(s)
    Singer, Barry A
    Alroughani, Raed
    Broadley, Simon
    Eichau, Sara
    Hartung, Hans-Peter
    Havrdova, Eva Kubala
    Kim, Ho Jin
    Nakamura, Kunio
    Navas, Carlos
    Pozzilli, Carlo
    Rovira, Alex
    Vermersch, Patrick
    Wray, Sibyl
    Chung, Luke
    Daizadeh, Nadia
    et al.
    Griffith University Author(s)
    Broadley, Simon
    Year published
    2019
    Metadata
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    Abstract
    Objective: Evaluate efficacy/safety of alemtuzumab over 8 years (y) in CARE-MS II patients. Background: In CARE-MS II (NCT00548405), alemtuzumab (12 mg/day; baseline: 5 days; 12 months later: 3 days) significantly improved clinical/MRI outcomes versus SC IFNB-1a over 2 y in relapsing-remitting MS (RRMS) patients with inadequate response to prior therapy. Efficacy was maintained in a 4-y extension (NCT00930553), in which patients could receive additional, as-needed alemtuzumab (12 mg/day on 3 days; ≥12 months apart) for disease activity or other disease-modifying therapy (DMT) per investigator discretion. Following the initial ...
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    Objective: Evaluate efficacy/safety of alemtuzumab over 8 years (y) in CARE-MS II patients. Background: In CARE-MS II (NCT00548405), alemtuzumab (12 mg/day; baseline: 5 days; 12 months later: 3 days) significantly improved clinical/MRI outcomes versus SC IFNB-1a over 2 y in relapsing-remitting MS (RRMS) patients with inadequate response to prior therapy. Efficacy was maintained in a 4-y extension (NCT00930553), in which patients could receive additional, as-needed alemtuzumab (12 mg/day on 3 days; ≥12 months apart) for disease activity or other disease-modifying therapy (DMT) per investigator discretion. Following the initial 4-y extension, patients could continue in TOPAZ (NCT02255656), an additional 5-y extension. Design/Methods: Patients in TOPAZ can receive additional alemtuzumab (≥12 months apart) or other DMT (at any time), both per investigator’s discretion. Results: 300/435 patients (69%) completed Y2 of TOPAZ (Y8 after initiating alemtuzumab). 44% received neither additional alemtuzumab nor another DMT through Y8. At Y8, annualized relapse rate was 0.18; 85% were relapse-free. From core study baseline to Y8, 70% of patients had stable/improved EDSS scores; mean EDSS score change was +0.17. Through Y8, 64% of patients were free of 6-month confirmed disability worsening; 47% attained 6-month confirmed disability improvement. In Y8, 58% of patients achieved no evidence of disease activity, 70% were free of MRI disease activity, 89% were free of new Gd-enhancing lesions, and 70% were free of new/enlarging T2 hyperintense lesions. Median cumulative brain volume loss (BVL) from baseline through Y8 was −1.06%; annual BVL was ≤0.19% in Y3–8. Incidence of overall adverse events (AEs) and infections decreased through Y8. Thyroid AE incidence peaked at 17% in Y3, declining thereafter. Conclusions: Efficacy of alemtuzumab on clinical, MRI, and BVL outcomes was maintained over 8 y without continuous treatment in CARE-MS II patients, with a consistent and manageable safety profile.
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    Conference Title
    Neurology
    Volume
    92
    Issue
    15 Supplement
    Publisher URI
    https://n.neurology.org/content/92/15_Supplement/P3.2-058
    Subject
    Clinical sciences
    Neurosciences
    Cognitive and computational psychology
    Science & Technology
    Life Sciences & Biomedicine
    Clinical Neurology
    Neurosciences & Neurology
    Publication URI
    http://hdl.handle.net/10072/393021
    Collection
    • Conference outputs

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