Evidence map›Paper›PMID 41168548›Full record

ArticleNeurology and therapy2025

Switching from Rituximab to Eculizumab in US Patients with Neuromyelitis Optica Spectrum Disorder: Impact on Hospitalizations.

Justin Lee, Adrian Kielhorn, Sami Fam, Emily Riser, Eoin P Flanagan

Abstract read
In one paragraph

Article in Neurology and therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Justin LeeAlexion, AstraZeneca Rare Disease, 121 Seaport Blvd, Boston, MA, USA.ORCID http://orcid.org/0009-0004-9689-5300
Adrian KielhornAlexion, AstraZeneca Rare Disease, 121 Seaport Blvd, Boston, MA, USA. adrian.kielhorn@alexion.com.ORCID http://orcid.org/0009-0006-4975-2045
Sami FamAlexion, AstraZeneca Rare Disease, 121 Seaport Blvd, Boston, MA, USA.
Emily RiserAlabama Neurology Associates, 3105 Independence Dr, Suite 105, Birmingham, AL, USA.
Eoin P FlanaganMayo Clinic, 200 First St. SW, Eighth Floor, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-6661-2910

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeuromyelitis optica spectrum disorder (NMOSD), a rare autoimmune disease, affects the optic nerves and spinal cord. Rituximab is often used off-label to treat NMOSD; however, comparator-controlled trial data are limited. Eculizumab is approved for treatment of anti-aquaporin-4 antibody-positive (AQP4-Ab+) NMOSD. Outcomes data for patients who switch from rituximab to eculizumab are limited.

methodsThis retrospective study used claims data from the IQVIA PharMetrics

resultsThe percentage of patients hospitalized in the switch group decreased after transitioning to eculizumab (45.0% vs. 10.0%; p = 0.034) corresponding to a decreased mean number of hospitalizations per patient from 1.1 to 0.1 (p = 0.005). The percentage of patients hospitalized in the control group was similar before and after the reference date (10.1% vs. 9.3%; p = 0.755) corresponding to a mean number of hospitalizations per patient of 0.160 and 0.156 (p = 0.922), respectively. In the switch group, median (interquartile range [IQR]) hospitalization duration decreased from 8.5 (5.0-11.0) days before switching to eculizumab to 2.5 (2.2-2.8) days after switching (p < 0.001). Median (IQR) hospitalization duration in the control group was 4.0 (2.0-9.0) days before and 4.0 (2.0-6.0) days after the reference date.

conclusionAlthough the claims-based analysis and small patient numbers limit generalizability, we observed a reduction in hospitalizations number and length of stay in a cohort of patients with NMOSD who switched from rituximab to eculizumab.

Indexed as

EculizumabHealthcare resource utilizationNeuromyelitis optica spectrum disorderRare diseaseRituximab

Identifiers

PMID41168548
PMCPMC12623551

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