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Conference/Presentation Title: | Predicting long-term sustained disability progression in multiple sclerosis. | Authors: | Van Wijmeersch B.;Malpas C.;Hupperts R.M.M.;Alroughani R.;Boz C.;Shaygannejad V.;Van Pesch V.;Kappos L.;Lechner-Scott J.;Bergamaschi R.;Turkoglu R.;Solaro C.;Ramo-Tello C.;Iuliano G.;Granella F.;Spitaleri D.L.A.;Bolanos R.F.;Slee M.;McCombe P.;Prevost J.;Ampapa R.;Ozakbas S.;Sanchez-Menoyo J.L.;Soysal A.;Vucic O.;Petersen T.;Verheul F.;Butler E. ;Hodgkinson S.;Sidhom Y.;Gouider R.;Cristiano E.;Urtaza F.J.O.;Saladino M.L.;Barnett M.;Deri N.;Moore F.;Rozsa C.;Yamout B.;Skibina O.;Gray O.;Campbell J.;Sempere A.;Singhal B.;Fragoso Y.;Shaw C.;Kermode A.;Petkovska-Boskova T.;Taylor B.;Simo M.;Vella N.;Shuey N.;Alkhaboori J.;Al-Harbi T.;Macdonell R.;Dominguez J.A.;Kister I.;Csepany T.;Vrech C.;Kovacs K.;Sirbu C.A.;Hughes S.;Sormani M.P.;Butzkueven H.;Kalincik T.;Sharmin S.;Bovis F.;Horakova D.;Havrdova E.;Ayuso G.I.;Eichau S.;Trojano M.;Prat A.;Girard M.;Duquette P.;Onofrj M.;Lugaresi A.;Grand'Maison F.;Grammond P.;Sola P.;Ferraro D.;Terzi M. | Institution: | (Sharmin, Malpas, Kalincik) CORe, University of Melbourne (Bovis, Sormani) University of Genoa (Horakova, Havrdova) Charles University (Ayuso) Servicio De Neurologia (Eichau) Hospital Universitario Virgen Macarena (Trojano) Policlinico-Bari (Prat) CHUM Hopital Norte Dame, Dept of Neurology (Girard) Hopital Notre Dame (Duquette) CHUM Notre-Dame (Onofrj) University G. d'Annunzio (Lugaresi) Univ. Di chieti-Pescara (Grand'Maison) Neuro Rive-Sud (Grammond) Hotel-Dieu De Levis Hospital (Sola) Nuovo Ospedale Civile S. Agostino-Estense (Ferraro) University of Modena and Reggio Emilia (Terzi) 19Mayis Universitesi (Hupperts) Biogen Int. B.V. (Alroughani) Amiri Hospital (Boz) KTU Medical Faculty Farabi Hospital (Shaygannejad) Isfahan University of Medical Sciences (Van Pesch) Cliniques St-Luc (Kappos) Neurology, University Hospital Basel (Lechner-Scott) Hunter New England Health (Bergamaschi) IRCCS Mondino Foundation (Turkoglu) Haydarpasa Numune Training and Research Hospital (Solaro) Neurology PA Micone Hospital (Ramo-Tello) Hospital Germans Trias i Pujol (Iuliano) Osp Riuniti San Giovanni Di Dio (Granella) Zeneca-UK (Van Wijmeersch) Rehabilitation and MS-Centre Overpelt (Spitaleri) A.O. 'S. Giuseppe Moscati' (Bolanos) Complejo Hospitalario Nuestra Senora de Valme (Slee) Flinders University (McCombe) University of Queensland (Prevost) Neurologie des Laurentides (Ampapa) Neurologicka Klinika Jihlava (Ozakbas) GenPharmaceuticals (Sanchez-Menoyo) Hospital de Galdakao-Usansolo (Soysal) Bakirkoy Hospital Of Mental Disorders And Neuro (Vucic) Westmead Hospital (Petersen) Arhus Sygehus (Verheul) Groene Hart Ziekenhuis (Butler) Monash Medical Centre (Hodgkinson) Liverpool Hospital (Sidhom) Department of Neurology (Gouider) Erazi Hospital (Cristiano) Hospital Italiano De Buenos Aires (Urtaza) Instituto de Investigacion Sanitaria Biodonostia (Saladino) INEBA-Institute of Neuroscience Buenos Aires (Barnett) Brain and Mind Centre (Deri) Merck Serono Argentina (Moore) Jewish General Hospital (Rozsa) Jahn Ferenc Teaching Hospital (Yamout) American University of Beirut (Skibina) Neurosciences, Box Hill Hospital (Gray) Ulster Hospital (Campbell) Craigavon Area Hospital (Sempere) Hospital General Universitario de Alicante (Singhal) Bombay Hospital Institute of Medical Sciences (Fragoso) Universidade Metropolitana de Santos (Shaw) Geelong Hospital (Kermode) SJOG Clinic, Suite 314 (Petkovska-Boskova) Clinic of Neurology Clinical Center (Taylor) Menzies Research Institue Tasmania (Simo) Semmelweis (Vella) Department of Neuroscience (Shuey) St Vincent'S Hospital (Alkhaboori) Royal Hospital (Al-Harbi) KFSHD (Macdonell) Waterdale Medical Rooms (Dominguez) Hospital Universitario de la Ribera (Kister) NYU School of Medicine, NY (Csepany) University of Debrecen (Vrech) Sanatorio Allende (Kovacs) Peterfy Sandor Hospital (Sirbu) Central Military Emergency University Hospital (Hughes) Royal Victoria Hospital (Butzkueven) Monash University | Presentation/Conference Date: | 14-Oct-2020 | Copyright year: | 2020 | Publisher: | Lippincott Williams and Wilkins | Publication information: | Neurology. Conference: 72nd Annual Meeting of the American Academy of Neurology, AAN 2020. Toronto, ON Canada. 94 (15 Supplement) (no pagination), 2020. Date of Publication: 2020. | Abstract: | Objective: Using global MSBase registry, this study establishes 6-month confirmed disability progression events as indicators of long-term disability worsening suitable for use in randomized clinical trials in multiple sclerosis (MS). Background(s): Randomized clinical trials evaluate short-term treatment effect on disability in the form of 3-6-month confirmed disability progression, but whether these translate into long-term disability outcomes is unknown. Design/Methods: A Cox proportional hazards model identified associations between patients' demographic and clinical characteristics and the probability of recovery from disability progression events. The coefficients from this model were used to calculate a sustained progression score, which was evaluated in a validation cohort and applied to a trial cohort. Result(s): 902 patients (development cohort), patient characteristics at the time of progression associated with lower probability of subsequent improvement were age (hazard ratio (HR)=0.98), primary progressive (HR=0.37) and progressive-relapsing (HR=0.36) MS, expanded disability status scale score >=6 (HR=0.71) and its change from baseline (HR=0.67), number of affected functional system scores (HR=0.92) and pyramidal (HR=0.79) functional system score (p<0.05). The strength of the association with pyramidal score decreased with time (HR=1.01). A relapse within previous month (HR=1.46) and worsening in sensory functional system score (HR=1.17) were associated with higher probability of improvement after progression. The sustained progression score (range 0.39-4.79) in the validation cohort with 1,271 progression events, estimated a 53% lower chance of improvement for each unit increase in the score (HR=0.47). The proportions of progression events sustained at 5 years stratified by the score were 1: 68%, 2: 79%, 3: 94%, 4: 100%. The progression scores were then applied to the CLARITY trial data. Conclusion(s): Estimate of the probability of disability progression events being sustained over the long term will enable future trials to establish the effect of therapy not only on the short-term but also on long-term disability accrual. | Conference Start Date: | 2020-04-25 | Conference End Date: | 2020-05-01 | ISSN: | 1526-632X | URI: | https://repository.monashhealth.org/monashhealthjspui/handle/1/35062 | Type: | Conference Abstract | Type of Clinical Study or Trial: | Randomised controlled trial |
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