The contribution of enhancing lesions in monitoring multiple sclerosis treatment: is gadolinium always necessary?


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 10 04 2020
accepted: 05 05 2020
revised: 03 05 2020
pubmed: 14 5 2020
medline: 22 6 2021
entrez: 14 5 2020
Statut: ppublish

Résumé

MRI is highly sensitive for monitoring of disease activity and treatment efficacy in MS. Patients treated with disease modifying therapy (DMT), who experience MRI activity, including contrast-enhancing lesions (CEL) or new/enlarged T2 lesions, should be evaluated for a switch to more effective treatment. Due to recent evidence of gadolinium (Gd) accumulation in the brain after repeated administration of Gd-based contrast agents, FDA recommended to limit its use. To investigate the proportion of cases in which MRI activity would be detectable only using contrast-enhanced T1-weighted sequences.Secondary aims were to assess the presence of clinical or demographic variables associated with reactivation of pre-existing lesions and to analyse therapeutic consequences of different types of MRI lesions. We retrospectively evaluated brain MRI scans, performed between 2014 and 2018, in patients treated with DMT for at least 6 months. We analysed 906 scans in 255 patients. New/enlarged T2 lesions were detected in 13.7% of cases, CEL in 3.5%, CEL without new T2 lesions (old lesions reactivated) in 1.1%. No variables were associated with old lesions reactivated. CEL with T2 equivalent were at higher risk of DMT switch, compared with new/enlarged T2 lesions without corresponding CEL (OR 4.0, 95% CI 1.5-10.4, p  = 0.005). Reactivation of pre-existing lesions is limited to a tiny fraction of MRI studies. Gd + T1-weighted images could be omitted, in patients treated with DMT for at least 6 months, without relevant loss of information.

Sections du résumé

BACKGROUND BACKGROUND
MRI is highly sensitive for monitoring of disease activity and treatment efficacy in MS. Patients treated with disease modifying therapy (DMT), who experience MRI activity, including contrast-enhancing lesions (CEL) or new/enlarged T2 lesions, should be evaluated for a switch to more effective treatment. Due to recent evidence of gadolinium (Gd) accumulation in the brain after repeated administration of Gd-based contrast agents, FDA recommended to limit its use.
AIM OBJECTIVE
To investigate the proportion of cases in which MRI activity would be detectable only using contrast-enhanced T1-weighted sequences.Secondary aims were to assess the presence of clinical or demographic variables associated with reactivation of pre-existing lesions and to analyse therapeutic consequences of different types of MRI lesions.
METHODS METHODS
We retrospectively evaluated brain MRI scans, performed between 2014 and 2018, in patients treated with DMT for at least 6 months.
RESULTS RESULTS
We analysed 906 scans in 255 patients. New/enlarged T2 lesions were detected in 13.7% of cases, CEL in 3.5%, CEL without new T2 lesions (old lesions reactivated) in 1.1%. No variables were associated with old lesions reactivated. CEL with T2 equivalent were at higher risk of DMT switch, compared with new/enlarged T2 lesions without corresponding CEL (OR 4.0, 95% CI 1.5-10.4, p  = 0.005).
CONCLUSIONS CONCLUSIONS
Reactivation of pre-existing lesions is limited to a tiny fraction of MRI studies. Gd + T1-weighted images could be omitted, in patients treated with DMT for at least 6 months, without relevant loss of information.

Identifiants

pubmed: 32399696
doi: 10.1007/s00415-020-09894-1
pii: 10.1007/s00415-020-09894-1
doi:

Substances chimiques

Contrast Media 0
Gadolinium AU0V1LM3JT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2642-2647

Auteurs

Elena Tsantes (E)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy. elena.tsantes@gmail.com.

E Curti (E)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy.

C Ganazzoli (C)

Neuroradiology Unit, Department of Diagnostic, Parma University Hospital, Parma, Italy.

F Puci (F)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy.

V Bazzurri (V)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy.

A Fiore (A)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy.

G Crisi (G)

Neuroradiology Unit, Department of Diagnostic, Parma University Hospital, Parma, Italy.

F Granella (F)

Neurosciences Unit, Department of Medicine and Surgery, University of Parma, via Gramsci 14, 43126, Parma, Italy.
Department of General Medicine, Multiple Sclerosis Centre, Parma University Hospital, Parma, Italy.

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Classifications MeSH