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Silent lesions on MRI imaging - Shifting goal posts for treatment decisions in multiple sclerosis.

Authors :
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
Min, Myintzu
Spelman, Tim
Lugaresi, Alessandra
Boz, Cavit
Spitaleri, Daniele LA
Pucci, Eugenio
Grand'Maison, Francois
Granella, Franco
Izquierdo, Guillermo
Butzkueven, Helmut
Sanchez-Menoyo, Jose Luis
Barnett, Michael
Girard, Marc
Trojano, Maria
Grammond, Pierre
Duquette, Pierre
Sola, Patrizia
Alroughani, Raed
Hupperts, Raymond
Vucic, Steve
Kalincik, Tomas
Van Pesch, Vincent
Lechner-Scott, Jeannette
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
Min, Myintzu
Spelman, Tim
Lugaresi, Alessandra
Boz, Cavit
Spitaleri, Daniele LA
Pucci, Eugenio
Grand'Maison, Francois
Granella, Franco
Izquierdo, Guillermo
Butzkueven, Helmut
Sanchez-Menoyo, Jose Luis
Barnett, Michael
Girard, Marc
Trojano, Maria
Grammond, Pierre
Duquette, Pierre
Sola, Patrizia
Alroughani, Raed
Hupperts, Raymond
Vucic, Steve
Kalincik, Tomas
Van Pesch, Vincent
Lechner-Scott, Jeannette
Source :
Multiple sclerosis (Houndmills, Basingstoke, England), Vol. 24, no.12, p. 1569-1577 (2018)
Publication Year :
2018

Abstract

The current best practice suggests yearly magnetic resonance imaging (MRI) to monitor treatment response in multiple sclerosis (MS) patients. To evaluate the current practice of clinicians changing MS treatment based on subclinical new MRI lesions alone. Using MSBase, an international MS patient registry with MRI data, we analysed the probability of treatment change among patients with clinically silent new MRI lesions. A total of 8311 MRI brain scans of 4232 patients were identified. Around 26.9% (336/1247) MRIs with one new T2 lesion were followed by disease-modifying therapy (DMT) change, increasing to 50.2% (129/257) with six new T2 lesions. DMT change was twice as likely with new T1 contrast enhancing compared to new T2 lesions odds ratio (OR): 2.43, 95% confidence interval (CI): 2.00-2.96 vs OR: 1.26 (95% CI: 1.22-1.29). DMT change with new MRI lesions occurred most frequently with 'injectable' DMTs. The probability of switching therapy was greater only after high-efficacy therapies became available in 2007 (after, OR: 1.43, 95% CI: 1.28-1.59 vs before, OR: 0.98, 95% CI: 0.520-1.88). MS clinicians rely increasingly on MRI alone in their treatment decisions, utilizing low thresholds (1 new T2 lesion) for optimizing MS therapy. This signals a shift towards no evidence of disease activity (NEDA)-3 since high-efficacy therapies became available.

Details

Database :
OAIster
Journal :
Multiple sclerosis (Houndmills, Basingstoke, England), Vol. 24, no.12, p. 1569-1577 (2018)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1130449067
Document Type :
Electronic Resource