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Switching therapies in MS – what is the evidence?

 

SPECIAL REPORT

It is now generally accepted that patients with relapsing-remitting multiple sclerosis will require more than one disease-modifying therapy (DMT) during their clinical course. Although a proportion of patients appear to be clinically stable on a platform therapy (beta-interferons and glatiramer acetate), it has been difficult to demonstrate the long-term benefits of this approach. A recent analysis of patients who initiated a DMT in the period 1995-2002 and received treatment for 13 years found no difference in time to onset of secondary-progressive MS (SPMS) between treated patients and untreated natural history cohorts (Coret et al. Mult Scler J Exp Transl Clin 2018;4:2055217318783347). Read More

AAN Poster Picks – Thursday, May 9, 2019

 

Here are Steven’s Poster Picks for Thursday, May 9, 2019:

Multiple sclerosis

  1. MRI predictors of disability (P5.2-001)
  2. Biomarkers: NfL and GFAP (P5.2-006, P5.2-007, P5.2-017, P5.2-021); OCBs (P5.2-014, P5.2-022)
  3. Lymphocyte kinetics: and alemtuzumab (P5.2-009)
  4. CIS and immune phenotype (P5.2-018)
  5. Sexual dysfunction (P5.2-089)
  6. Cannabis: in BC (P5.2-092), and spasticity (P5.2-100, P5.2-106)

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AAN Poster Picks – Wednesday, May 8, 2019

 

Here are Steven’s Poster Picks for Wednesday, May 8, 2019:

Multiple sclerosis

  1. Pregnancy: use of natalizumab (P4.2-093, P4.2-105), anti-CD20 therapies (P4.2-094), DMF (P4.2-095), outcomes with DMT exposure (P4.2-100), NfL levels (P4.2-092)
  2. Pediatric: OCBs (P4.2-104), cognitive impairment (P4.6-035)
  3. JCV Ab index (P4.2-009, P4.2-040)
  4. Rare adverse events – case reports: Ocrelizumab (P4.2-010), fingolimod (P4.2-011, P4.2-012, P4.2-016, P4.2-036), cladribine (P4.2-022), alemtuzumab (P4.2-027)
  5. Pharmacogenetics and cladribine (P4.2.044)

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