https://doi.org/10.55788/31dbb369
Many RRMS patients choose to start with a disease-modifying therapy (DMT) that has low or moderate efficacy, to then escalate this therapy when necessary, as opposed to starting with an early, intensive therapy. According to Dr Dalia Rotstein (University of Toronto, Canada), such an escalation approach can be considered due to favourable prognostic factors, long-term safety concerns, patient preference (in terms of safety and route of administration), access, or associated cost [1]. She emphasised that treatment response should consequently be assessed early. “MS is a highly heterogeneous disease which is largely unpredictable, especially early on. So, the first 1 or 2 years of therapy can provide valuable information to determine what treatment intensity is required in the long term.” In these first 2 years, the patient should be closely monitored for relapses, MRI activity, and disability progression, while also considering levels of neurofilament light (NfL).
No randomised-controlled trials exist to date to guide treatment switches. When considering a switch, the neurologist should take the time to treatment effect (varying from 3–6 months) into account, and then obtain a re-baseline MRI. Generally in guidelines, 1 or more relapses are usually seen as a cause for concern, as well as a confirmed Expanded Disability Status Scale (EDSS)-progression of at least 1 point. More controversy exists regarding MRI, but anywhere between 1–3 new T2 lesions should be a reason to consider a switch.
To avoid delays in escalating therapy, vaccination in advance (especially in the COVID-19 era) is important. According to Dr Rotstein, the washout period should be minimised. In recent studies, prolonged washout periods have been associated with an elevated risk of new disease activity, particularly after terminating fingolimod treatment [2]. She concluded that early aggressive therapy (the “hit-hard-and-early” concept) may gain popularity, but the escalation approach continues to be a viable paradigm, in view of varying disease severity, medication safety, and patient preference.
- Rotstein DL. How to make a timely switch to high efficacy DMT. Abstract O006, ECTRIMS 2022, 26–28 October, Amsterdam, the Netherlands.
- Alroughani R, et al. Mult Scler Relat Disord. 2019;34:9–13.
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Table of Contents: ECTRIMS 2022
Featured articles
Letter from the Editor
Diagnosis and Prediction of Disease Course
A case for including optic nerve lesions in the McDonald criteria
Cerebrospinal fluid kappa-free light chains for MS diagnosis
Early, non-disabling relapses increase disability accumulation
Physical impairment is present before perceived MS onset
Chronic active MS lesions respond poorly to anti-CD20 antibodies
Treatment: Trials & Strategies
Dimethyl fumarate reduces the risk of a first clinical event in RIS
How and when to make a timely switch to high-efficacy DMT
Comparing real-world effectiveness of DMTs
Study fails to show non-inferiority of rituximab to ocrelizumab
Autologous haematopoietic stem cell transplantation versus DMTs
Progressive MS
Stem cell transplantation not superior to natalizumab in progressive MS
Efficacy of DMTs fades away in secondary progressive MS
Smartphone tapping can help detect progressive MS
Paediatric MS
Early treatment with DMT effective in paediatric-onset MS
Fingolimod in paediatric MS: results of up to 6 years
Switching treatment after initial platform injectable DMT: real-world data
Pregnancy
Pregnancy and infant outcomes in women receiving ocrelizumab
New safety data of anti-CD20 mAbs around pregnancy
MS activity and pregnancy outcomes after long-term use of natalizumab
NMOSD
Ravulizumab significantly reduced relapses in AQP4+ NMOSD
NMOSD patients are cognitively impaired regardless of serostatus
Evidence-based consensus on pregnancy in NMOSD
COVID-19
COVID-19 and MS: lessons learned thus far
Ocrelizumab and fingolimod increase the risk of COVID-19 and of worse outcomes
Humoral and cellular immune responses after SARS-CoV-2 vaccination
Miscellaneous
Re-myelination strategies in MS still pose many unanswered questions
MS associated with a broader Epstein-Barr virus specific T-cell receptor repertoire
Cognitive rehab and mindfulness reduce cognitive complaints in MS
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