This protocol applies to patients with active relapsing-remitting multiple sclerosis who continue to experience clinical relapses and MRI activity — including contrast-enhancing lesions or new/unequivocally enlarging T2 lesions on brain MRI — despite having received an initial disease-modifying drug.
The preceding step involved early treatment with a disease-modifying drug — selected from a spectrum ranging from modestly effective to highly efficacious agents — chosen according to patient characteristics, comorbidities, disease severity and activity, and drug safety profile. Escalation to this protocol is warranted when the required treatment targets are not met: persistence of clinical relapses, disability progression, or MRI activity (new or enlarging T2 lesions, or gadolinium-enhancing lesions) on standardised brain MRI at 6 and 12 months from treatment onset.
DOI: 10.1177/1352458517751049
Offer early treatment with DMDs to patients with active RRMS as defined by clinical relapses and/or MRI activity (active lesions–contrast-enhancing lesions; new or unequivocally enlarging T2 lesions assessed at least annually).
Offer a more efficacious drug to patients treated with interferon or glatiramer acetate who show evidence of disease activity assessed as recommended in questions 4–5 of this guideline.
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