Evidence map›Paper›PMID 40702280›Full record

ArticleJournal of neurology2025

Comparing the efficacy and safety of cyclophosphamide, infliximab and methotrexate in neurosarcoidosis: a multicenter retrospective study.

Hélène Gomez, Nicolas Noël, Jean Schmidt, Achille Aouba, Bertrand Bourre, Vincent Langlois, Marine Avenel, Ygal Benhamou, Mathilde Leclercq

Abstract readMulticenter StudyComparative Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 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

9 authors.

Hélène GomezDepartment of Internal Medicine, University Hospital Charles Nicolle, 76 000, Rouen, France. Helene.gomez@chu-rouen.fr.ORCID http://orcid.org/0009-0008-2761-843X
Nicolas NoëlDepartment of Internal Medicine, Assistance Publique-Hôpitaux de Paris, University Hospital Paris Sud, 94 275, Le Kremlin-Bicêtre, France.
Jean SchmidtDepartment of Internal Medicine, University Hospital Amiens-Picardie, 60 000, Amiens, France.
Achille AoubaDepartment of Internal Medicine, University Hospital Caen-Normandie, 14 000, Caen, France.
Bertrand BourreDepartment of Neurology, University Hospital Charles Nicolle, 76 000, Rouen, France.
Vincent LangloisDepartment of Internal Medicine, Hospital Jacques Monod, 76 600, Le Havre, France.
Marine AvenelDepartment of Internal Medicine, Intercommunal Hospital Elbeuf-Louviers-Val de Reuil, 76 500, Elbeuf, France.
Ygal BenhamouDepartment of Internal Medicine, University Hospital Charles Nicolle, 76 000, Rouen, France.
Mathilde LeclercqDepartment of Internal Medicine, University Hospital Charles Nicolle, 76 000, Rouen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeurosarcoidosis is a granulomatous disease affecting 10% of patients with sarcoidosis. In lack of standardized guidelines, various therapeutic strategies exist. Beyond corticosteroids, cyclophosphamide, infliximab, or methotrexate are available options. This study compared the efficacy and safety of these agents as firstline therapy.

methodsThis multicenter, retrospective, study included patients with definite or probable neurosarcoidosis (1999-2022). Primary endpoint was relapse rate at the end of follow-up, after first-line therapy with cyclophosphamide, infliximab or methotrexate. Relapse was defined as a≥1-point increase in the Extrapulmonary Organ Severity Tool score following initial improvement.

resultsFifty-two patients were included: 18 (34.6%) received cyclophosphamide, 10 (19.2%) infliximab and 24 (46.2%) methotrexate. Multivisceral impairment was observed in 63% of patients, and neurological involvement at diagnosis in 67% of patients. Main neurological localizations were the brain (60%), meninges (48%) and cranial nerves (46%). Sixteen patients (30.7%) relapsed: 56% with cyclophosphamide, 6% with infliximab and 38% with methotrexate (p = 0.06). Median relapse-free survival was 48 months in patients treated with cyclophosphamide, and not estimable for infliximab or methotrexate (p = 0.07). Relapse was associated with brain involvement (p = 0.006) and younger age (p = 0.04). At 12 months, response rate was 100% for infliximab-treated patients, 89% for cyclophosphamide and 87% for methotrexate. All treatments demonstrated a corticosteroid-sparing effect, with infliximab achieving the highest proportion of patients (80%) reaching ≤ 5 mg/day at 12 months (p = 0.07). Infections were more frequent with cyclophosphamide (p = 0.01), however two deadly infections occured with methotrexate.

conclusionInfliximab and methotrexate appear as effective and safe options for relapse prevention in neurosarcoidosis.

Indexed as

Central Nervous System DiseasesCyclophosphamideImmunosuppressive AgentsInfliximabMethotrexateSarcoidosisAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedRecurrenceRetrospective StudiesTreatment OutcomeCyclophosphamideImmunosuppressive AgentsInfliximabMethotrexateCyclophosphamideInfliximabMethotrexateNeurosarcoidosisRelapse

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Registered trials

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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.