Evidence map›Paper›PMID 41160790›Full record

ArticleNeurology2025

Effectiveness of Infliximab for Refractory Nonischemic Cerebral Enhancing Foreign-Body Granulomatous Lesions After Endovascular Therapy.

Albert Aboseif, Farris Taha, Nathan Troy Tagg, Andrew D Smith, Eoin P Flanagan, Robert D Brown, Sean J Pittock, Gina S Perez Giraldo, Andrew McKeon

Abstract readCase ReportsMulticenter Study
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
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.

Albert AboseifDepartment of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-5053-8544
Farris TahaDepartment of Neurology, Washington University, St. Louis, MO.ORCID 0009-0005-6257-2500
Nathan Troy TaggDepartments of Neurology & Ophthalmology, Duke University School of Medicine, Durham, NC.
Andrew D SmithMultiple Sclerosis Center, Dartmouth-Hitchcock Medical Center and Geisel School of Medicine Dartmouth College, Dartmouth, NH.ORCID 0000-0003-3002-222X
Eoin P FlanaganDepartment of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-6661-2910
Robert D BrownDepartment of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-7065-8807
Sean J PittockDepartment of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-6140-5584
Gina S Perez GiraldoDepartment of Neurology, Medical University of South Carolina, Charleston.ORCID 0000-0002-8798-3753
Andrew McKeonDepartment of Neurology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-6856-8143

Funding

Washington University Institute of Clinical and Translational Sciences (TL1)TL1TR002344 · NCATS · WASHINGTON UNIVERSITY · PI Jay F. Piccirillo · 2017 to 2026
$8.5M
Utilizing epidemiology, imaging and fluid biomarkers in MOG antibody-associated disease to inform prognosis, pathogenesis and therapeuticsR01NS113828 · NINDS · MAYO CLINIC ROCHESTER · PI Eoin P Flanagan · 2020 to 2026
$2.4M
NCATS NIH HHS TL1 TR002344NINDS NIH HHS R01 NS113828
6 · The paper itself

Abstract

objectivesNonischemic cerebral enhancing (NICE) foreign-body granulomatous lesions are an immune-mediated complication of endovascular therapy (EVT). No single immunotherapy has demonstrated consistent effectiveness. We highlight the novel use of tumor necrosis factor (TNF)-α inhibition in treating refractory NICE lesions.

methodsThis multicenter case series describes 3 patients with refractory NICE lesions (recurrent seizures, persistent MRI enhancement, and/or steroid dependence with failure of ≥1 maintenance immunotherapy) treated with infliximab. Their clinical course, evaluation, and outcomes are detailed.

resultsPatients were women (median age 57 years [range 56-58]), presenting with headache and seizures within 6 months of EVT for intracranial aneurysm (n = 2) or carotid stenosis (n = 1). MRI (n = 3) revealed unilateral nodular enhancement with vasogenic edema, and brain biopsy (n = 2) revealed foreign-body granulomatous inflammation. All patients developed refractory disease and steroid dependence despite ≥1 immunotherapy including mycophenolate (n = 3), rituximab (n = 1), and/or cyclophosphamide (n = 1). Infliximab treatment resulted in significant clinical and radiologic improvement in all 3 patients. DISCUSSION: TNF-α inhibition may be an effective targeted treatment strategy for NICE foreign-body granulomatous lesions, expanding treatment options for patients with refractory disease. Larger prospective studies are needed to establish treatment guidelines aimed at improving outcomes in individuals with refractory disease. CLASSIFICATION OF EVIDENCE: This article provides Class IV evidence that infliximab may offer potential benefit in patients with NICE lesions after EVT.

Indexed as

Endovascular ProceduresGranuloma, Foreign-BodyInfliximabFemaleHumansIntracranial AneurysmMagnetic Resonance ImagingMiddle AgedTreatment OutcomeInfliximab

Identifiers

PMID41160790
PMCPMC12810356

What OpenQuestion holds

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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.