Disability progression in relapse-free multiple sclerosis patients on fingolimod versus interferon-beta/glatiramer

Viktor von Wyl1, Pascal Benkert2, André Moser3

  • 1Department of Epidemiology, Biostatistics and Prevention Institute, University of Zürich, Zürich, Switzerland/ Swiss Multiple Sclerosis Registry, Epidemiology, Biostatistics and Prevention Institute, University of Zürich, Zürich, Switzerland.

Multiple Sclerosis (Houndmills, Basingstoke, England)
|May 29, 2020
PubMed
Abstract

Insights

Fingolimod significantly reduces disability progression in relapsing-remitting multiple sclerosis (RRMS) compared to interferon-beta/glatiramer acetate (IFN/GA). This benefit was observed in both relapsing and relapse-free patients, highlighting fingolimod

Area of Science:

  • Neurology
  • Immunology
  • Clinical Trials

Background:

  • Disability progression independent of relapses (PIRA) is a frequent occurrence in relapsing-remitting multiple sclerosis (RRMS).
  • Understanding factors influencing PIRA is crucial for optimizing treatment strategies in RRMS.

Purpose of the Study:

  • To compare the incidence of disability progression in relapse-free RRMS patients treated with interferon-beta/glatiramer acetate (IFN/GA) versus fingolimod.
  • To evaluate the efficacy of fingolimod in preventing disability progression, considering both relapsing and relapse-free disease courses.

Main Methods:

  • Retrospective analysis of 1640 RRMS patients from Swiss health insurance data.
  • Comparison of time to relapse and 12-month confirmed disability progression using multivariable Cox regression.
  • Application of inverse-probability weighting to correct for biases in treatment group selection.

Main Results:

  • Fingolimod use was associated with a significantly lower frequency of disability progression compared to IFN/GA (HR=0.53).
  • This protective effect of fingolimod remained significant even after bias correction and in relapse-free patients (HR=0.56).
  • Disability progression was observed in 8.8% of IFN/GA patients and 7.6% of fingolimod patients.

Conclusions:

  • Fingolimod demonstrates superior efficacy over IFN/GA in preventing disability progression in young, newly diagnosed RRMS patients.
  • The benefits of fingolimod extend to both relapsing and relapse-free disease states, suggesting a broad impact on disease course.

Related Concept Videos

Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids01:21

Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids

Glucocorticoids, a class of anti-inflammatory drugs, are pivotal in treating moderate to severe Crohn's disease by inducing remission. They exhibit their anti-inflammatory action by inhibiting the production of inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1, and chemokines like IL-8. In addition, they reduce the expression of inflammatory cell adhesion molecules and inhibit gene transcription of nitric oxide synthase, phospholipase A2, cyclooxygenase-2...
347
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF01:24

Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF

Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab...
374
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents01:29

Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents

Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel...
381