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10.1177/13524585211028833

http://scihub22266oqcxt.onion/10.1177/13524585211028833
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34240631!9131403!34240631
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suck abstract from ncbi


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pmid34240631      Mult+Scler 2022 ; 28 (7): 1121-1125
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  • Personalized B-cell tailored dosing of ocrelizumab in patients with multiple sclerosis during the COVID-19 pandemic #MMPMID34240631
  • van Lierop ZY; Toorop AA; van Ballegoij WJ; Olde Dubbelink TB; Strijbis EM; de Jong BA; van Oosten BW; Moraal B; Teunissen CE; Uitdehaag BM; Killestein J; Kempen ZLV
  • Mult Scler 2022[Jun]; 28 (7): 1121-1125 PMID34240631show ga
  • In this observational study, 159 patients with multiple sclerosis received personalized dosing of ocrelizumab incentivized by the COVID-19 pandemic. Re-dosing was scheduled when CD19 B-cell count was ?10 cells/microL (starting 24 weeks after the previous dose, repeated 4-weekly). Median interval until re-dosing or last B-cell count was 34 [30-38] weeks. No clinical relapses were reported and a minority of patients showed Expanded Disability Status Scale (EDSS) progression. Monthly serum neurofilament light levels remained stable during extended intervals. Two (1.9%) of 107 patients with a follow-up magnetic resonance imaging (MRI) scan showed radiological disease activity. Personalized dosing of ocrelizumab could significantly extend intervals with low short-term disease activity incidence, encouraging future research on long-term safety and efficacy.
  • |*COVID-19[MESH]
  • |*Multiple Sclerosis, Relapsing-Remitting/drug therapy/epidemiology[MESH]
  • |*Multiple Sclerosis/drug therapy/epidemiology[MESH]
  • |Antibodies, Monoclonal, Humanized[MESH]
  • |Humans[MESH]


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