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      Overall Disability Response Score: An integrated endpoint to assess disability improvement and worsening over time in patients with multiple sclerosis

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          Abstract

          Background:

          Overall Disability Response Score (ODRS) is a composite endpoint including Expanded Disability Status Scale, Timed 25-foot Walk, and 9-Hole Peg Test, designed to quantify both disability improvement and worsening in multiple sclerosis (MS).

          Objective:

          To assess the sensitivity and clinical meaningfulness of ODRS using natalizumab Phase 3 data sets (AFFIRM in relapsing-remitting MS and ASCEND in secondary progressive MS).

          Methods:

          Differences in ODRS over 96 weeks, ODRS at Week 96, and slope of ODRS change per year between natalizumab and placebo groups were analyzed. Correlation between ODRS and changes in patient-reported outcomes was also analyzed.

          Results:

          The difference (95% confidence interval (CI)) in the ODRS over 96 weeks between natalizumab and placebo groups was 0.34 (0.21–0.46) in AFFIRM ( p < 0.001), and 0.18 (0.03–0.34) in ASCEND ( p = 0.021). Significant differences between treatment arms were also observed in ODRS at Week 96 and in the slope of change per year in both studies. There was a significant linear correlation between ODRS at Week 96 and the change from baseline in both the physical and mental components of the 36-item Short Form Survey (SF-36) in both studies.

          Conclusion:

          This analysis supports ODRS as a sensitive and potentially clinically meaningful disability outcome measure in MS.

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          Most cited references36

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          Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS).

          J. Kurtzke (1983)
          One method of evaluating the degree of neurologic impairment in MS has been the combination of grades (0 = normal to 5 or 6 = maximal impairment) within 8 Functional Systems (FS) and an overall Disability Status Scale (DSS) that had steps from 0 (normal) to 10 (death due to MS). A new Expanded Disability Status Scale (EDSS) is presented, with each of the former steps (1,2,3 . . . 9) now divided into two (1.0, 1.5, 2.0 . . . 9.5). The lower portion is obligatorily defined by Functional System grades. The FS are Pyramidal, Cerebellar, Brain Stem, Sensory, Bowel & Bladder, Visual, Cerebral, and Other; the Sensory and Bowel & Bladder Systems have been revised. Patterns of FS and relations of FS by type and grade to the DSS are demonstrated.
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            Multiple Sclerosis

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              A randomized, placebo-controlled trial of natalizumab for relapsing multiple sclerosis.

              Natalizumab is the first alpha4 integrin antagonist in a new class of selective adhesion-molecule inhibitors. We report the results of a two-year phase 3 trial of natalizumab in patients with relapsing multiple sclerosis. Of a total of 942 patients, 627 were randomly assigned to receive natalizumab (at a dose of 300 mg) and 315 to receive placebo by intravenous infusion every four weeks for more than two years. The primary end points were the rate of clinical relapse at one year and the rate of sustained progression of disability, as measured by the Expanded Disability Status Scale, at two years. Natalizumab reduced the risk of sustained progression of disability by 42 percent over two years (hazard ratio, 0.58; 95 percent confidence interval, 0.43 to 0.77; P<0.001). The cumulative probability of progression (on the basis of Kaplan-Meier analysis) was 17 percent in the natalizumab group and 29 percent in the placebo group. Natalizumab reduced the rate of clinical relapse at one year by 68 percent (P<0.001) and led to an 83 percent reduction in the accumulation of new or enlarging hyperintense lesions, as detected by T2-weighted magnetic resonance imaging (MRI), over two years (mean numbers of lesions, 1.9 with natalizumab and 11.0 with placebo; P<0.001). There were 92 percent fewer lesions (as detected by gadolinium-enhanced MRI) in the natalizumab group than in the placebo group at both one and two years (P<0.001). The adverse events that were significantly more frequent in the natalizumab group than in the placebo group were fatigue (27 percent vs. 21 percent, P=0.048) and allergic reaction (9 percent vs. 4 percent, P=0.012). Hypersensitivity reactions of any kind occurred in 25 patients receiving natalizumab (4 percent), and serious hypersensitivity reactions occurred in 8 patients (1 percent). Natalizumab reduced the risk of the sustained progression of disability and the rate of clinical relapse in patients with relapsing multiple sclerosis. Adhesion-molecule inhibitors hold promise as an effective treatment for relapsing multiple sclerosis. (ClinicalTrials.gov number, NCT00027300.). Copyright 2006 Massachusetts Medical Society.
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                Author and article information

                Contributors
                Journal
                Mult Scler
                Mult Scler
                MSJ
                spmsj
                Multiple Sclerosis (Houndmills, Basingstoke, England)
                SAGE Publications (Sage UK: London, England )
                1352-4585
                1477-0970
                21 September 2022
                December 2022
                : 28
                : 14
                : 2263-2273
                Affiliations
                [1-13524585221114997]Cerevel Therapeutics, Cambridge, MA, USA
                [2-13524585221114997]Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), Departments of Head, Spine and Neuromedicine, Clinical Research, Biomedicine and Biomedical Engineering, University Hospital Basel, University of Basel, Basel, Switzerland
                [3-13524585221114997]Barts and The London School of Medicine and Dentistry, Queen Mary University, London, UK
                [4-13524585221114997]The Johns Hopkins Multiple Sclerosis Center, Baltimore, MD, USA
                [5-13524585221114997]Voyager Therapeutics, Cambridge, MA, USA
                [6-13524585221114997]Biogen, Cambridge, MA, USA
                [7-13524585221114997]Takeda Pharmaceuticals, Lexington, MA, USA
                [8-13524585221114997]Biogen, Cambridge, MA, USA
                [9-13524585221114997]Biogen, Cambridge, MA, USA
                [10-13524585221114997]Upstream Bio, Waltham, MA, USA
                [11-13524585221114997]Biogen, Cambridge, MA, USA
                Author notes
                [*]B Zhu Biogen, 225 Binney Street, Cambridge, MA 02142, USA. bing.zhu@ 123456biogen.com
                [*]

                Former employees of Biogen

                Author information
                https://orcid.org/0000-0003-4175-5509
                https://orcid.org/0000-0002-7776-6472
                https://orcid.org/0000-0002-3975-4366
                Article
                10.1177_13524585221114997
                10.1177/13524585221114997
                9732786
                36131595
                1476adc6-24bf-4ec3-849f-a1202823fe10
                © The Author(s), 2022

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 24 February 2022
                : 21 June 2022
                : 3 July 2022
                Funding
                Funded by: Biogen, FundRef https://doi.org/10.13039/100005614;
                Categories
                Original Research Papers
                Measurement
                Custom metadata
                ts1

                Immunology
                disability worsening,disability improvement,disability progression,multicomponent outcome measure,odrs,relapsing-remitting multiple sclerosis,secondary progressive multiple sclerosis

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