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Current therapeutic landscape in multiple sclerosis: an evolving treatment paradigm

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F19%3A73598968" target="_blank" >RIV/61989592:15110/19:73598968 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://journals.lww.com/co-neurology/fulltext/2019/06000/Current_therapeutic_landscape_in_multiple.9.aspx" target="_blank" >https://journals.lww.com/co-neurology/fulltext/2019/06000/Current_therapeutic_landscape_in_multiple.9.aspx</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1097/WCO.0000000000000700" target="_blank" >10.1097/WCO.0000000000000700</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Current therapeutic landscape in multiple sclerosis: an evolving treatment paradigm

  • Popis výsledku v původním jazyce

    Purpose of review To critically assess the current landscape of disease-modifying agents for multiple sclerosis ( MS). Treatment algorithms will be discussed and studies for new agents in late development or recently approved are analyzed in terms of their impact on current treatment strategies. Recent findings A real-world study from Wales suggests that early initiation of highly effective therapy may provide more benefit that an escalation approach in relapsing MS. A study from the MSBase dataset found evidence that early treatment with highly effective therapies decreased the risk of developing secondary progressive MS. Ocrelizumab is highly efficacious in relapsing MS and in a group of patients with primary progressive MS. Another CD20 directed mAb, ofatumumab, is in phase 3. A large study examining extended interval dosing of natalizumab in an attempt to decrease the risk of developing progressive multifocal leukoencephalopathy is underway. Cladribine and alemtuzumab may work by immune reconstitution. Siponimod was recently approved by United States Federal Drug Administration for relapsing MS and active secondary progressive MS. Other S1P receptor modulators are being studied in phase 3 trials for relapsing MS. Cladribine received FDA approval as treatment for relapsing and active secondary progressive MS. Autologous hematopoetic stem-cell transplantation may be an option for treatment-refractory MS.

  • Název v anglickém jazyce

    Current therapeutic landscape in multiple sclerosis: an evolving treatment paradigm

  • Popis výsledku anglicky

    Purpose of review To critically assess the current landscape of disease-modifying agents for multiple sclerosis ( MS). Treatment algorithms will be discussed and studies for new agents in late development or recently approved are analyzed in terms of their impact on current treatment strategies. Recent findings A real-world study from Wales suggests that early initiation of highly effective therapy may provide more benefit that an escalation approach in relapsing MS. A study from the MSBase dataset found evidence that early treatment with highly effective therapies decreased the risk of developing secondary progressive MS. Ocrelizumab is highly efficacious in relapsing MS and in a group of patients with primary progressive MS. Another CD20 directed mAb, ofatumumab, is in phase 3. A large study examining extended interval dosing of natalizumab in an attempt to decrease the risk of developing progressive multifocal leukoencephalopathy is underway. Cladribine and alemtuzumab may work by immune reconstitution. Siponimod was recently approved by United States Federal Drug Administration for relapsing MS and active secondary progressive MS. Other S1P receptor modulators are being studied in phase 3 trials for relapsing MS. Cladribine received FDA approval as treatment for relapsing and active secondary progressive MS. Autologous hematopoetic stem-cell transplantation may be an option for treatment-refractory MS.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30210 - Clinical neurology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    CURRENT OPINION IN NEUROLOGY

  • ISSN

    1350-7540

  • e-ISSN

  • Svazek periodika

    32

  • Číslo periodika v rámci svazku

    3

  • Stát vydavatele periodika

    US - Spojené státy americké

  • Počet stran výsledku

    13

  • Strana od-do

    365-377

  • Kód UT WoS článku

    000480723400008

  • EID výsledku v databázi Scopus

    2-s2.0-85065348368