This is a randomized pragmatic clinical trial fully embedded in the Swiss Multiple Sclerosis Cohort to assess whether sNfL biomarker monitoring improves patient-relevant outcomes and care of patients with relapsing-remitting (RR)MS by either increasing the proportion of patients with no evidence of disease activity (EDA) or by improving patients' health-related quality of life.
The course of multiple sclerosis (MS) is highly heterogenous with a large variability in symptoms, severity and response to treatment. A large majority of persons with MS are treated with disease modifying therapies (DMTs). DMTs can dramatically reduce even almost suppress relapses and occurrence of new lesions in magnetic resonance imaging (MRI) by weakening the immune system but which in turn may cause side effects such as opportunistic infections with prolonged treatment duration and intensity of the immunosuppression. A more personalized approach to MS therapy is urgently needed to treat patients as little as possible but as much as necessary and at the right time. Such tailored strategies cannot be made without detailed information on treatment response and disease activity. Levels sNfL, which is released in the blood following neuroaxonal damage, has been shown to be associated with future MS disease activity, disability worsening, MRI activity and treatment response. sNfL might therefore be helpful for a patient-tailored treatment adaptation (e.g., escalation or de-escalation) ensuring disease stability, fewer adverse events and better quality of life. While sNfL is increasingly used as a marker of treatment response, its use in routine care is not yet widely established. The SMSC is an observational study across 8 Swiss leading MS centers including \>1600 participants with MS with a median follow-up of \>5.7 years. The MultiSCRIPT project aims to use this real-world data infrastructure to systematically evaluate patient-relevant benefits resulting from innovations in MS patient care. MultiSCRIPT goes beyond a unique trial but aims to be a sustainable learning system in which accumulating data from successive pragmatic randomized trials (i.e., learning cycles) enable the continuous generation of new hypotheses on how treatment and care strategies can be further personalized to treat patients as little as possible but as much as necessary at the right time. By being nested within the already existing and ongoing SMSC, this research infrastructure embedded in clinical care offers an unique opportunity to efficiently conduct a nationwide real-life evaluation of new care strategies, at low costs, and fostering evaluation and direct translation of effective innovations into usual care to improve patient outcome and quality of life. MultiSCRIPT-Cycle 1 is the first learning cycle.
the intervention consist of a blood draw and providing the sNfL information to the treating physician
University Hospital Basel
Basel, Canton of Basel-City, Switzerland
Kantonsspital Aarau
Aarau, Switzerland
Inselspital Bern
Bern, Switzerland
Hôpitaux Universitaires de Genève
Geneva, Switzerland
EDA3 (evidence of disease activity)
number of participant with a relapse or disability worsening (measured by Expanded Disability Status Scale (EDSS)) or disease activity on MRI imaging (new/enlarging T2 weighted lesions or T1 weighted contrast enhancing lesion on cranial or spinal cord MRI)
Time frame: 24-months
Multiple Sclerosis Quality of Life (MSQOL)-54 Instrument
The summary scores are the physical health composite summary and the mental health composite summary. A higher score indicates improved quality of life
Time frame: 24-months
Multiple Sclerosis Quality of Life (MSQOL)-54 Instrument
The summary scores are the physical health composite summary and the mental health composite summary. A higher score indicates improved quality of life
Time frame: 12-months
EDA3 (evidence of disease activity)
number of participant with a relapse or disability worsening (measured by Expanded Disability Status Scale (EDSS)) or disease activity on MRI imaging (new/enlarging T2 weighted lesions or T1 weighted contrast enhancing lesion on cranial or spinal cord MRI)
Time frame: 12-months
EQ-5D-5L
The EQ-5D-5L descriptive system comprises the following five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression and includes an overall visual analog scale
Time frame: 12- and 24-months
Short form 36 (SF-36)
contained in the MSQoL-54 questionnaire. The lower the score the more disability.
Time frame: 12- and 24-months
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Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
920
Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
Ospedale Regionale di Lugano, sede Civico
Lugano, Switzerland
Kantonsspital St.Gallen
Sankt Gallen, Switzerland
UniversitätsSpital Zürich
Zurich, Switzerland
relapses
according to McDonald criteria
Time frame: 12- and 24-months
disability worsening
measured by Expanded Disability Status Scale (EDSS). The EDSS ranges from 0 to 10. The greater the level of disability, the higher is the score.
Time frame: 12- and 24-months
New/enlarging T2w lesions
MRI imaging
Time frame: 12- and 24-months
T1w contrast enhancing lesions
MRI imaging
Time frame: 12- and 24-months
Amount of immunosuppressive/immunomodulatory drug treatment
Time frame: 12- and 24-months