Evidence map›Paper›PMID 40098899›Full record

ArticleTherapeutic advances in neurological disorders2025

Evaluating natalizumab first-line and later-line use in multiple sclerosis: a US claims database analysis.

Robin L Avila, Nicole S Croteau, Fei Tang, Jason C Simeone, Khalil Jomaa, Boyang Bian, Mattia Gianinazzi

Abstract read
In one paragraph

Article in Therapeutic advances in neurological disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Robin L AvilaBiogen,US Medical Rare Diseases, Cambridge, MA 02142, USA.
Nicole S CroteauCytel, Evidence, Value and Access, Cambridge, MA, USA.ORCID https://orcid.org/0000-0001-5017-1834
Fei TangCytel, Evidence, Value and Access, Cambridge, MA, USA.
Jason C SimeoneCytel, Evidence, Value and Access, Cambridge, MA, USA.ORCID https://orcid.org/0000-0002-6141-8043
Khalil JomaaBiogen, Value and Access - Global/International Regions, Paris, France.
Boyang BianBiogen, NA Medical Evidence Generation, Cambridge, MA, USA.
Mattia GianinazziBiogen, Value and Market Access, Baar, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Limited information exists on the healthcare resource utilization (HCRU) associated with real-world natalizumab used as a first-line (1L) versus later-line (2L+) treatment in multiple sclerosis (MS). Objectives: To describe natalizumab use in newly diagnosed MS patients treated as 1L or 2L+ and evaluate unadjusted annualized relapse rates (ARR) and MS-related HCRU before and after treatment initiation. Design: This retrospective observational study utilized Komodo Health Sentinel claims data from October 2015 to August 2022. The study included adults diagnosed with incident MS who initiated natalizumab treatment, with insurance coverage for at least 12 months before diagnosis and 24 months after. The index date was the first natalizumab claim on or after the diagnosis. Baseline was defined as the 365 days prior to the index date, truncated at the time of diagnosis. Follow-up ended at the earliest occurrence of death, insurance disenrollment, treatment discontinuation (gap ⩾45 days), switch to another disease-modifying therapy before natalizumab discontinuation, or study end. Methods: Relapses and HCRU were assessed using person-time methods to account for varying follow-up times. Relapses were identified using a validated claims-based algorithm, and time to first relapse was analyzed using Kaplan-Meier methods. Hazard ratios for relapse were estimated using univariate Cox models. Mean differences (MD) in HCRU between baseline and follow-up and between 1L and 2L+ treatment groups were calculated. Results: A total of 1174 patients in the 1L group (mean age 39.0, 72.0% female) and 394 in the 2L+ group (mean age 39.7, 79.4% female) were included. Patients in the 1L group had a significantly higher baseline ARR (1.48 vs 0.92, Conclusion: Natalizumab as a first-line treatment was associated with greater reductions in ARR and MS-related HCRU compared to later-line use.

Indexed as

healthcare resource utilizationmultiple sclerosisrelapsetreatment patterns

Identifiers

PMID40098899
PMCPMC11912164

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.