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