BACKGROUND AND PURPOSE: Treatment options in primary progressive multiple sclerosis (PPMS) are scarce and, with the exception of ocrelizumab, anti-inflammatory agents have failed to show efficacy in ameliorating disability progression. The aim of this study was to investigate a potential effect of anti-inflammatory disease-modifying treatment on disability outcomes in PPMS. METHODS: Using MSBase, a large, international, observational database, we identified patients with PPMS who were either never treated or treated with a disease-modifying agent. Propensity score matching was used to select subpopulations with similar baseline characteristics. Expanded Disability Status Scale (EDSS) outcomes were compared with an intention-to-treat and an as-treated approach in paired, pairwise-censored analyses. RESULTS: Of the 1284 included patients, 533 were matched (treated, n = 195; untreated n = 338). Median on-study pairwise-censored follow-up was 3.4 years (quartiles 1.2-5.5). No difference in the hazard of experiencing 3-month confirmed EDSS progression events was observed between the groups [hazard ratio (HR), 1.0; 95% confidence interval (CI), 0.6-1.7, P = 0.87]. We did not find significant differences in the hazards of confirmed EDSS improvement (HR, 1.0; 95% CI, 0.6-1.6, P = 0.91) or reaching a confirmed EDSS step ≥7 (HR, 1.1; 95% CI, 0.7-1.6, P = 0.69). CONCLUSION: Our pooled analysis of disease-modifying agents suggests that these therapies have no substantial effect on short- to medium-term disability outcomes in PPMS.

Anti-inflammatory disease-modifying treatment and disability progression in primary progressive multiple sclerosis: a cohort study / Lorscheider, J; Kuhle, J; Izquierdo, G; Lugaresi, A; Havrdova, E; Horakova, D; Hupperts, R; Duquette, P; Girard, M; Prat, A; Grand'Maison, F; Grammond, P; Sola, P; Ferraro, D; Trojano, M; Ramo-Tello, C; Lechner-Scott, J; Pucci, E; Solaro, C; Slee, M; Van Pesch, V; Sanchez Menoyo, J L; van der Walt, A; Butzkueven, H; Kappos, L; Kalincik, T. - In: EUROPEAN JOURNAL OF NEUROLOGY. - ISSN 1351-5101. - ELETTRONICO. - 26:2(2019), pp. 363-370. [10.1111/ene.13824]

Anti-inflammatory disease-modifying treatment and disability progression in primary progressive multiple sclerosis: a cohort study

Lugaresi, A
Writing – Review & Editing
;
2019

Abstract

BACKGROUND AND PURPOSE: Treatment options in primary progressive multiple sclerosis (PPMS) are scarce and, with the exception of ocrelizumab, anti-inflammatory agents have failed to show efficacy in ameliorating disability progression. The aim of this study was to investigate a potential effect of anti-inflammatory disease-modifying treatment on disability outcomes in PPMS. METHODS: Using MSBase, a large, international, observational database, we identified patients with PPMS who were either never treated or treated with a disease-modifying agent. Propensity score matching was used to select subpopulations with similar baseline characteristics. Expanded Disability Status Scale (EDSS) outcomes were compared with an intention-to-treat and an as-treated approach in paired, pairwise-censored analyses. RESULTS: Of the 1284 included patients, 533 were matched (treated, n = 195; untreated n = 338). Median on-study pairwise-censored follow-up was 3.4 years (quartiles 1.2-5.5). No difference in the hazard of experiencing 3-month confirmed EDSS progression events was observed between the groups [hazard ratio (HR), 1.0; 95% confidence interval (CI), 0.6-1.7, P = 0.87]. We did not find significant differences in the hazards of confirmed EDSS improvement (HR, 1.0; 95% CI, 0.6-1.6, P = 0.91) or reaching a confirmed EDSS step ≥7 (HR, 1.1; 95% CI, 0.7-1.6, P = 0.69). CONCLUSION: Our pooled analysis of disease-modifying agents suggests that these therapies have no substantial effect on short- to medium-term disability outcomes in PPMS.
2019
Anti-inflammatory disease-modifying treatment and disability progression in primary progressive multiple sclerosis: a cohort study / Lorscheider, J; Kuhle, J; Izquierdo, G; Lugaresi, A; Havrdova, E; Horakova, D; Hupperts, R; Duquette, P; Girard, M; Prat, A; Grand'Maison, F; Grammond, P; Sola, P; Ferraro, D; Trojano, M; Ramo-Tello, C; Lechner-Scott, J; Pucci, E; Solaro, C; Slee, M; Van Pesch, V; Sanchez Menoyo, J L; van der Walt, A; Butzkueven, H; Kappos, L; Kalincik, T. - In: EUROPEAN JOURNAL OF NEUROLOGY. - ISSN 1351-5101. - ELETTRONICO. - 26:2(2019), pp. 363-370. [10.1111/ene.13824]
Lorscheider, J; Kuhle, J; Izquierdo, G; Lugaresi, A; Havrdova, E; Horakova, D; Hupperts, R; Duquette, P; Girard, M; Prat, A; Grand'Maison, F; Grammond, P; Sola, P; Ferraro, D; Trojano, M; Ramo-Tello, C; Lechner-Scott, J; Pucci, E; Solaro, C; Slee, M; Van Pesch, V; Sanchez Menoyo, J L; van der Walt, A; Butzkueven, H; Kappos, L; Kalincik, T
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/653897
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