Evidence map›Paper›PMID 41585216›Full record

ArticleFrontiers in medicine2025

Real-world use of ixekizumab for axial spondyloarthritis treatment in Spain (ESPADA study).

Cristina Campos, Ma Concepción Fito-Manteca, Cristina Valero-Martínez, Sara García-Carazo, Raquel Almodóvar, Silvia Díaz-Cerezo, Sebastián Moyano, Amelia Cobo, Itxaso Aguirregabiria, Clara Pérez-Rambla and 2 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 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. Article
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

12 authors.

Cristina CamposRheumatology Department, General University Hospital of Valencia, Valencia, Spain.
Ma Concepción Fito-MantecaRheumatology Department, University Hospital of Navarra, Navarra, Spain.
Cristina Valero-MartínezRheumatology Department, University Hospital La Princesa, Madrid, Spain.
Sara García-CarazoRheumatology Department, University Hospital La Paz, IdiPaz, Madrid, Spain.
Raquel AlmodóvarRheumatology Department, University Hospital Fundación Alcorcón, Madrid, Spain.
Silvia Díaz-CerezoEli Lilly and Company, Alcobendas, Spain.
Sebastián MoyanoEli Lilly and Company, Alcobendas, Spain.
Amelia CoboEli Lilly and Company, Alcobendas, Spain.
Itxaso AguirregabiriaEli Lilly and Company, Alcobendas, Spain.
Clara Pérez-RamblaOutcomes'10 SLU (Product Life Group), Castellón de la Plana, Spain.
Francisco Javier Pérez-SádabaOutcomes'10 SLU (Product Life Group), Castellón de la Plana, Spain.
Victoria Navarro-CompánRheumatology Department, University Hospital La Paz, IdiPaz, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: While ixekizumab (IXE) has demonstrated efficacy in axial spondyloarthritis (axSpA) clinical trials, real-world evidence is limited. This study describes the characteristics and treatment persistence of axSpA patients receiving IXE in routine clinical practice in Spain. Methods: A retrospective study of axSpA patients treated with IXE was carried out in ten hospitals. Demographic, clinical, treatment-related characteristics, persistence and disease activity were collected at baseline, 12, 24 and 52 weeks. Descriptive analysis and Kaplan-Meier methods were used. Results: The study included 106 axSpA patients, 69.8% had r-axSpA, 58.5% were male, and 63% had overweight or obesity. Mean (SD) disease duration was 12.8 (12.3) years. 98.1% had received b/tsDMARDs and 52.5% presented normal C-reactive protein (CRP) levels at baseline. Persistence rates were 99.0, 80.5, and 56.3% at 12, 24, and 52 weeks, respectively. At week 52, 33.3% fewer patients had high/very high disease activity according to Ankylosing Spondylitis Disease Activity Index (ASDAS-CRP) scores and 18.9% showed an improvement of ≥50% in their Bath Ankylosing Spondylitis Disease Activity Index (BASDAI). Exploratory subanalyses showed IXE persistence was not influenced by gender, smoking status, BMI, axSpA clinical form, CRP levels, HLA-B27 status, prior biological (b) or targeted synthetic (ts) DMARD (b/tsDMARD) or secukinumab. IXE was discontinued by 40 (37.7%) patients during follow-up, mainly due to lack of effectiveness. Conclusion: Most axSpA patients treated with IXE had long-standing, highly active disease involving multiple domains and prior multiple domains and prior b/tsDMARDs (b/tsDMARD) exposure. Despite this, half remained on IXE at 1 year with improved disease activity, highlighting its potential as a treatment option in daily practice.

Indexed as

axial spondyloarthritisclinical responseixekizumabreal-world studytreatment persistence

Identifiers

PMID41585216
PMCPMC12827647

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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.