Evidence map›Paper›PMID 41714331›Full record

Observational studyScientific reports2026

Ixekizumab for the treatment of psoriatic arthritis: an Italian multicentric retrospective observational study.

Stefano Gentileschi, Riccardo Terribili, Carla Gaggiano, Elisa Fiorentini, Laura Cometi, Cosimo Cigolini, Fabio Massimo Perrotta, Silvia Scriffignano, Luca Di Cato, Anna Panaccione and 9 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in Scientific reports, 2026. 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

19 authors.

Stefano GentileschiRheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena University Hospital, viale Mario Bracci 16, 53100, Siena, Italy.
Riccardo TerribiliRheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena University Hospital, viale Mario Bracci 16, 53100, Siena, Italy.
Carla GaggianoRheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena University Hospital, viale Mario Bracci 16, 53100, Siena, Italy. cgaggiano132@gmail.com.ORCID http://orcid.org/0000-0003-1401-8343
Elisa FiorentiniDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, 50134, Florence, Italy.
Laura CometiDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, 50134, Florence, Italy.
Cosimo CigoliniRheumatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, 56124, Pisa, Italy.
Fabio Massimo PerrottaAcademic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, 86100, Campobasso, Italy.
Silvia ScriffignanoAcademic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, 86100, Campobasso, Italy.
Luca Di CatoRheumatology Unit, Santa Maria General Hospital, 05100, Terni, Italy.
Anna PanaccioneRheumatology Unit, Santa Maria General Hospital, 05100, Terni, Italy.
Laura NiccoliRheumatology Unit, S. Stefano Hospital, 59100, Prato, Italy.
Fabrizio CantiniRheumatology Unit, S. Stefano Hospital, 59100, Prato, Italy.
Maurizio BenucciRheumatology Unit, S. Giovanni Di Dio Firenze Hospital, 50134, Florence, Italy.
Francesca Li GobbiRheumatology Unit, S. Giovanni Di Dio Firenze Hospital, 50134, Florence, Italy.
Andrea Delle SedieRheumatology Unit, Department of Clinical and Experimental Medicine, University of Pisa, 56124, Pisa, Italy.
Antonio VitaleRheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena University Hospital, viale Mario Bracci 16, 53100, Siena, Italy.
Ennio LubranoAcademic Rheumatology Unit, Department of Medicine and Health Sciences "Vincenzo Tiberio", University of Molise, 86100, Campobasso, Italy.
Bruno FredianiRheumatology Unit, Department of Medicine, Surgery and Neurosciences, University of Siena, Siena University Hospital, viale Mario Bracci 16, 53100, Siena, Italy.
Serena GuiducciDepartment of Experimental and Clinical Medicine, Division of Rheumatology, University of Florence, 50134, Florence, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ixekizumab (IXE), an IL-17 A inhibitor, demonstrated efficacy in clinical trials in patients with psoriatic arthritis (PsA), and favorable data have emerged from real-world evidence studies on psoriasis as well. However, real-world data specific to PsA remain limited. This study aims to assess IXE effectiveness in reducing disease activity in patients with PsA and determine its drug retention rate (DRR) over 24 months. The secondary aim is to identify factors potentially affecting long-term persistence on therapy. A retrospective observational study was conducted. Consecutive adult patients meeting the CASPAR criteria for PsA and treated with IXE for ≥ 3 months were included. Patients were evaluated at regular intervals on a routine clinical basis for disease activity and quality of life assessment. 132 patients (78 females, 54 males; mean age 59.1 ± 11.9 years) were included. At baseline, the median (IQR) Disease Activity in Psoriatic Arthritis (DAPSA) was 16.2 (7.7), and the visual analogue scale (VAS) for pain was 6.5 (3.0). In patients with axial involvement, the median (IQR) Ankylosing Spondylitis Disease Activity Score – C-reactive protein (ASDAS-CRP) was 3.4 (1.3), and the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) was 5.0 (1.5). IXE treatment was associated with statistically significant reductions in DAPSA (p < 0.001), ASDAS-CRP (p < 0.001), BASDAI (p < 0.001), VAS-pain (p < 0.001), Health Assessment Questionnaire (HAQ) (p < 0.001), erythrocyte sedimentation rate (p = 0.014), and CRP (p = 0.004) over 24 months. At 24 months, remission and low disease activity, according to DAPSA thresholds, were achieved by 46.7% and 93.3% of patients, respectively, while Very Low Disease Activity and Minimal Disease Activity criteria were met by 16.0% and 34.0%, respectively. IXE DRR was 82.1%, 76.3%, and 73.3% at 12, 18, and 24 months, respectively, with lower values in female patients (p = 0.036). No differences were observed in IXE DRR when stratifying the cohort by axial involvement (p = 0.84), prior exposure to biologics or tsDMARDs (p = 0.68), or body mass index (BMI) categories (p = 0.48). In conclusion, IXE enabled rapid and sustained disease control in patients with PsA across multiple disease domains. The high DRR supports its long-term use, regardless of prior biologic exposure or BMI. Gender differences in IXE treatment response may warrant further exploration.

Indexed as

Antibodies, Monoclonal, HumanizedArthritis, PsoriaticAdultAgedFemaleHumansItalyMaleMiddle AgedQuality of LifeRetrospective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedixekizumabInterleukin-17IxekizumabPsoriatic arthritisReal-world evidence

Identifiers

PMID41714331
PMCPMC12920993

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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 Socratic graph.