Initial high-efficacy disease-modifying therapy in multiple sclerosis: A nationwide cohort study

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Initial high-efficacy disease-modifying therapy in multiple sclerosis : A nationwide cohort study. / Buron, Mathias Due; Chalmer, Thor Ameri; Sellebjerg, Finn; Barzinji, Ismael; Christensen, Jeppe Romme; Christensen, Mette Kirstine; Hansen, Victoria; Illes, Zsolt; Jensen, Henrik Boye; Kant, Matthias; Papp, Viktoria; Petersen, Thor; Rasmussen, Peter Vestergaard; Schäfer, Jakob; Theódórsdóttir, Ásta; Weglewski, Arkadiusz; Sorensen, Per Soelberg; Magyari, Melinda.

I: Neurology, Bind 95, Nr. 8, 2020, s. e1041-e1051.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Buron, MD, Chalmer, TA, Sellebjerg, F, Barzinji, I, Christensen, JR, Christensen, MK, Hansen, V, Illes, Z, Jensen, HB, Kant, M, Papp, V, Petersen, T, Rasmussen, PV, Schäfer, J, Theódórsdóttir, Á, Weglewski, A, Sorensen, PS & Magyari, M 2020, 'Initial high-efficacy disease-modifying therapy in multiple sclerosis: A nationwide cohort study', Neurology, bind 95, nr. 8, s. e1041-e1051. https://doi.org/10.1212/WNL.0000000000010135

APA

Buron, M. D., Chalmer, T. A., Sellebjerg, F., Barzinji, I., Christensen, J. R., Christensen, M. K., Hansen, V., Illes, Z., Jensen, H. B., Kant, M., Papp, V., Petersen, T., Rasmussen, P. V., Schäfer, J., Theódórsdóttir, Á., Weglewski, A., Sorensen, P. S., & Magyari, M. (2020). Initial high-efficacy disease-modifying therapy in multiple sclerosis: A nationwide cohort study. Neurology, 95(8), e1041-e1051. https://doi.org/10.1212/WNL.0000000000010135

Vancouver

Buron MD, Chalmer TA, Sellebjerg F, Barzinji I, Christensen JR, Christensen MK o.a. Initial high-efficacy disease-modifying therapy in multiple sclerosis: A nationwide cohort study. Neurology. 2020;95(8):e1041-e1051. https://doi.org/10.1212/WNL.0000000000010135

Author

Buron, Mathias Due ; Chalmer, Thor Ameri ; Sellebjerg, Finn ; Barzinji, Ismael ; Christensen, Jeppe Romme ; Christensen, Mette Kirstine ; Hansen, Victoria ; Illes, Zsolt ; Jensen, Henrik Boye ; Kant, Matthias ; Papp, Viktoria ; Petersen, Thor ; Rasmussen, Peter Vestergaard ; Schäfer, Jakob ; Theódórsdóttir, Ásta ; Weglewski, Arkadiusz ; Sorensen, Per Soelberg ; Magyari, Melinda. / Initial high-efficacy disease-modifying therapy in multiple sclerosis : A nationwide cohort study. I: Neurology. 2020 ; Bind 95, Nr. 8. s. e1041-e1051.

Bibtex

@article{9ac9f88c80494b89a2aa52a6b87ce01b,
title = "Initial high-efficacy disease-modifying therapy in multiple sclerosis: A nationwide cohort study",
abstract = "OBJECTIVE: To determine the effectiveness of high-efficacy disease-modifying therapies (heDMTs) vs medium-efficacy disease-modifying therapies (meDMT) as the first treatment choice in treatment-naive patients with multiple sclerosis (MS) on disability worsening and relapses. We assessed this using a nationwide population-based MS registry. METHODS: We identified all patients starting a heDMT as first-time treatment from the Danish Multiple Sclerosis Registry and compared treatment outcomes with a propensity score matched sample of patients starting meDMT. RESULTS: We included 388 patients in the study: 194 starting initial therapy with heDMT matched to 194 patients starting meDMT. At 4 years of follow-up, the probabilities of a 6-month confirmed Expanded Disability Status Scale (EDSS) score worsening were 16.7% (95% confidence interval [CI] 10.4%-23.0%) and 30.1% (95% CI 23.1%-37.1%) for heDMT and meDMT initiators, respectively (hazard ratio [HR] 0.53, 95% CI 0.33-0.83, p = 0.006). Patients initiating heDMT also had a lower probability of a first relapse (HR 0.50, 95% CI 0.37-0.67). Results were similar after pairwise censoring and in subgroups with high baseline activity, diagnosis after 2006, or information on baseline T2 lesion load. CONCLUSION: We found a lower probability of 6-month confirmed EDSS score worsening and lower probability of a first relapse in patients starting a heDMT as first therapy, compared to a matched sample starting meDMT. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that for patients with MS, starting heDMT lowers the risk of EDSS worsening and relapses compared to starting meDMT.",
author = "Buron, {Mathias Due} and Chalmer, {Thor Ameri} and Finn Sellebjerg and Ismael Barzinji and Christensen, {Jeppe Romme} and Christensen, {Mette Kirstine} and Victoria Hansen and Zsolt Illes and Jensen, {Henrik Boye} and Matthias Kant and Viktoria Papp and Thor Petersen and Rasmussen, {Peter Vestergaard} and Jakob Sch{\"a}fer and {\'A}sta The{\'o}d{\'o}rsd{\'o}ttir and Arkadiusz Weglewski and Sorensen, {Per Soelberg} and Melinda Magyari",
year = "2020",
doi = "10.1212/WNL.0000000000010135",
language = "English",
volume = "95",
pages = "e1041--e1051",
journal = "Neurology",
issn = "0028-3878",
publisher = "Lippincott Williams & Wilkins",
number = "8",

}

RIS

TY - JOUR

T1 - Initial high-efficacy disease-modifying therapy in multiple sclerosis

T2 - A nationwide cohort study

AU - Buron, Mathias Due

AU - Chalmer, Thor Ameri

AU - Sellebjerg, Finn

AU - Barzinji, Ismael

AU - Christensen, Jeppe Romme

AU - Christensen, Mette Kirstine

AU - Hansen, Victoria

AU - Illes, Zsolt

AU - Jensen, Henrik Boye

AU - Kant, Matthias

AU - Papp, Viktoria

AU - Petersen, Thor

AU - Rasmussen, Peter Vestergaard

AU - Schäfer, Jakob

AU - Theódórsdóttir, Ásta

AU - Weglewski, Arkadiusz

AU - Sorensen, Per Soelberg

AU - Magyari, Melinda

PY - 2020

Y1 - 2020

N2 - OBJECTIVE: To determine the effectiveness of high-efficacy disease-modifying therapies (heDMTs) vs medium-efficacy disease-modifying therapies (meDMT) as the first treatment choice in treatment-naive patients with multiple sclerosis (MS) on disability worsening and relapses. We assessed this using a nationwide population-based MS registry. METHODS: We identified all patients starting a heDMT as first-time treatment from the Danish Multiple Sclerosis Registry and compared treatment outcomes with a propensity score matched sample of patients starting meDMT. RESULTS: We included 388 patients in the study: 194 starting initial therapy with heDMT matched to 194 patients starting meDMT. At 4 years of follow-up, the probabilities of a 6-month confirmed Expanded Disability Status Scale (EDSS) score worsening were 16.7% (95% confidence interval [CI] 10.4%-23.0%) and 30.1% (95% CI 23.1%-37.1%) for heDMT and meDMT initiators, respectively (hazard ratio [HR] 0.53, 95% CI 0.33-0.83, p = 0.006). Patients initiating heDMT also had a lower probability of a first relapse (HR 0.50, 95% CI 0.37-0.67). Results were similar after pairwise censoring and in subgroups with high baseline activity, diagnosis after 2006, or information on baseline T2 lesion load. CONCLUSION: We found a lower probability of 6-month confirmed EDSS score worsening and lower probability of a first relapse in patients starting a heDMT as first therapy, compared to a matched sample starting meDMT. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that for patients with MS, starting heDMT lowers the risk of EDSS worsening and relapses compared to starting meDMT.

AB - OBJECTIVE: To determine the effectiveness of high-efficacy disease-modifying therapies (heDMTs) vs medium-efficacy disease-modifying therapies (meDMT) as the first treatment choice in treatment-naive patients with multiple sclerosis (MS) on disability worsening and relapses. We assessed this using a nationwide population-based MS registry. METHODS: We identified all patients starting a heDMT as first-time treatment from the Danish Multiple Sclerosis Registry and compared treatment outcomes with a propensity score matched sample of patients starting meDMT. RESULTS: We included 388 patients in the study: 194 starting initial therapy with heDMT matched to 194 patients starting meDMT. At 4 years of follow-up, the probabilities of a 6-month confirmed Expanded Disability Status Scale (EDSS) score worsening were 16.7% (95% confidence interval [CI] 10.4%-23.0%) and 30.1% (95% CI 23.1%-37.1%) for heDMT and meDMT initiators, respectively (hazard ratio [HR] 0.53, 95% CI 0.33-0.83, p = 0.006). Patients initiating heDMT also had a lower probability of a first relapse (HR 0.50, 95% CI 0.37-0.67). Results were similar after pairwise censoring and in subgroups with high baseline activity, diagnosis after 2006, or information on baseline T2 lesion load. CONCLUSION: We found a lower probability of 6-month confirmed EDSS score worsening and lower probability of a first relapse in patients starting a heDMT as first therapy, compared to a matched sample starting meDMT. CLASSIFICATION OF EVIDENCE: This study provides Class III evidence that for patients with MS, starting heDMT lowers the risk of EDSS worsening and relapses compared to starting meDMT.

U2 - 10.1212/WNL.0000000000010135

DO - 10.1212/WNL.0000000000010135

M3 - Journal article

C2 - 32636328

AN - SCOPUS:85089922758

VL - 95

SP - e1041-e1051

JO - Neurology

JF - Neurology

SN - 0028-3878

IS - 8

ER -

ID: 255840675