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Although some disease-modified therapies (DMTs) have been approved in the past decade, the treatment of relapsing-remitting multiple sclerosis remains challenging.
Alemtuzumab (ALEM) is an anti-CD52 monoclonal antibody that has been shown to control in untreated patients (CARE-MS I) and patients with poor response to first-line DMT (CARE-MS II) Very effective in disease activity.
Management consensus However, in patients who previously did not respond to fingolimod (FTY), the evidence for the effectiveness of ALEM has been conflicting.
Eleven adult patients with active MS who were considered eligible for ALEM treatment according to the latest prescribing standards were included in the prospective planned cohort study (NCT04082260).
immunity
Clinical data is also needed to assess the potential impact of DMT sequencing on the immune system to assist the decision-making process in clinical practice.
Blood vessel
170 patients who did not respond to NTZ, FTY, IFN or DMF at the beginning of treatment or before were identified and received at least two courses of ALEM treatment.
Regression analysis showed that among all the previously used DMT, the Fingemod pretreatment group (first relapse time n=33 hours (HR 5.
In a medical setting, this article proves that patients who have previously received Fengliemod have poor disease control after alemtuzumab treatment, and the risk of secondary autoimmunity is increased.
PfeufferS ,RuckT ,PulR PfeufferSPfeuffer RuckTRuck PulRPul, et albmj.
com/content/early/2021/03/11/jnnp-2020-325304" target="_blank" rel="noopener">Impact of previous disease-modifying treatment on effectiveness and safety outcomes, among patients with multiple sclerosis treated with alemtuzumabJournal of Neurology, Neurosurgery & Psychiatry Published Online First: 12 March 2021.
Published Online First: doi: 10.
1136/jnnp-2020-325304doi:Leave a message here