Conference Coverage

Satralizumab reduces risk of severe NMOSD relapse


 

FROM MSVirtual2020

Does satralizumab differ from other new agents?

The main strength of the study is that sufficient numbers of relapses were available for analysis in the active and control groups, said Achim Berthele, MD, associate professor of neurology at the Technical University of Munich. This allowed the researchers to examine whether satralizumab led to a better outcome after each relapse, which it did. “A weakness is how the severity of relapses was quantified,” said Dr. Berthele. “The EDSS as a measure is not linear, and its functional systems are not clinically equivalent. However, the whole NMOSD community is struggling with this problem.”

The study’s implications for neurologists’ clinical practice are unclear, however. “Although the results presented are encouraging, the data are still too small to say with certainty that satralizumab does indeed improve the outcome of relapses,” said Dr. Berthele. “It is also an open question whether satralizumab differs in this respect from the other new immunotherapeutic agents.”

Investigators must collect further data on the outcome of relapses that occur during treatment with modern immunomodulatory therapy, Dr. Berthele added. Future research could examine whether the new anti-inflammatory immunotherapeutic agents also are suitable drugs for relapse therapy. Another salient question is whether clinical vigilance or relapse therapy in NMOSD has improved in general. “This is what Kleiter and colleagues show as well: The number of severe relapses under placebo was much lower than expected,” said Dr. Berthele.

Chugai/Roche funded the study. Dr. Kleiter has received compensation for consulting, speaking, or serving on advisory boards for Alexion, Biogen, Celgene, Merck, and Roche. Dr. Berthele was not involved in any of the satralizumab trials, but is an investigator and coauthor of the PREVENT trial of eculizumab.

SOURCE: Kleiter I, et al. MSVirtual2020. Abstract FC01.03.

Pages

Recommended Reading

Secondary progressive MS: Sustained immunotherapy may improve disability outcomes
ICYMI Multiple Sclerosis
Personalized extended interval dosing does not reduce efficacy of natalizumab in MS
ICYMI Multiple Sclerosis
Efficacy of disease-modifying therapies in treatment-naïve patients with MS
ICYMI Multiple Sclerosis
Lower urinary tract dysfunction in patients with MS
ICYMI Multiple Sclerosis
Lowering rituximab dose in patients with MS proves safe and effective
ICYMI Multiple Sclerosis
Smoking increases risk of high plasma NfL levels in patients with MS
ICYMI Multiple Sclerosis
In MS, serious adverse effects are more common in rituximab versus ocrelizumab
ICYMI Multiple Sclerosis
Exposure to DMT may delay disability accumulation in primary progressive MS
ICYMI Multiple Sclerosis
Lessons for patients with MS and COVID-19
ICYMI Multiple Sclerosis
Cardiovascular risk factors linked to brain atrophy in MS
ICYMI Multiple Sclerosis