Evidence map›Paper›PMID 43007639›Full record

ArticleRheumatology and therapy2026

Two-Year Treatment Persistence and Effectiveness of Ixekizumab in Psoriatic Arthritis in Italian Clinical Practice: Results from the ROUTE-IXE Study.

Michele Maria Luchetti Gentiloni, Rosario Foti, Carlo Selmi, Francesco Cipollone, Florenzo Iannone, Lorenzo Dagna, Luca Idolazzi, Maria Sole Chimenti, Stefano Gentileschi, Roberta Ramonda and 9 more

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Article in Rheumatology and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Michele Maria Luchetti Gentiloni *Clinica Medica, Department of Internal Medicine, Marche University Hospital, Ancona, Italy.
Rosario Foti *Division of Rheumatology, AOU Policlinico "G. Rodolico" San Marco, Catania, Italy.
Carlo SelmiDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Francesco CipolloneRheumatology Unit, "Clinica Medica" Institute, Ospedale SS. Annunziata di Chieti, G. d'Annunzio University of Chieti, Chieti, Italy.
Florenzo IannoneUnit of Rheumatology, Department of Precision and Regenerative Medicine, Area Jonica (DiMePRe-J) University of Bari, Bari, Italy.
Lorenzo DagnaUnit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR), IRCCS San Raffaele Scientific Institute and Vita-Salute San Raffaele University, Milan, Italy.
Luca IdolazziRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Maria Sole ChimentiRheumatology, Allergology and Clinical Immunology, Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy.
Stefano GentileschiRheumatology Unit, Department of Medical, Surgical and Neurological Sciences, University of Siena and Azienda Ospedaliero-Universitaria Senese, Siena, Italy.
Roberta RamondaRheumatology Unit, Department of Medicine (DIMED), Padova University Hospital, Padua, Italy.
Francesco CicciaRheumatology Unit, Department of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Alen ZabottiRheumatology Clinic, Department of Medicine, University of Udine-Azienda Sanitaria Universitaria Friuli Centrale , Udine, Italy.
Ennio LubranoAcademic Rheumatology Unit, Department of Medicine and Health Sciences Vincenzo Tiberio, University of Molise, Campobasso, Italy.
Roberto CaporaliRheumatology Clinic, Department of Rheumatology and Medical Sciences, ASST G. Pini-CTO, Milan, Italy.
Maria Antonietta D'AgostinoDivision of Rheumatology, University Cattolica del Sacro Cuore-Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Alessia ScarliniEli Lilly S.P.A., Via Gramsci 731/733, 50019, Sesto Fiorentino, FI, Italy.
Stefania IppatiEli Lilly S.P.A., Via Gramsci 731/733, 50019, Sesto Fiorentino, FI, Italy. stefania.ippati@lilly.com.ORCID http://orcid.org/0000-0001-8408-6216
Federica GiurdanellaEli Lilly S.P.A., Via Gramsci 731/733, 50019, Sesto Fiorentino, FI, Italy.
Arianna AvitabileEli Lilly S.P.A., Via Gramsci 731/733, 50019, Sesto Fiorentino, FI, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRandomised controlled trials have demonstrated the efficacy and safety of ixekizumab as a treatment for active psoriatic arthritis (PsA), and real-world evidence on long-term persistence and effectiveness is emerging. This study aimed to characterise ixekizumab use in the Italian routine clinical setting and provide insights into its persistence and effectiveness, complementing real-world evidence from single-country cohorts and multinational studies.

methodsThis descriptive, multicentre, retrospective study was conducted in Italy in adult patients with PsA who received a first prescription of ixekizumab after January 2021 and had a minimum of three subsequent evaluations. The primary objective was to describe treatment persistence at week 104. Secondary objectives aimed to describe patients' demographic and clinical characteristics and evaluate treatment persistence and effectiveness at weeks 12, 24, 52 and 104.

resultsA total of 204 patients, of whom 88 (43.1%) were male and 116 (56.9%) were female, were eligible for inclusion in the study. The mean (standard deviation) age was 55.8 (11.0) years. Comorbidities were present in 66.7% (n = 136) of patients, with the majority being cardiometabolic disorders. The median (interquartile range) disease duration was 5.3 (2.4-12.2) years. Peripheral joint involvement was the most common PsA manifestation (66.7%, n = 136), followed by mixed symptoms (28.4%, n = 58) and axial-only symptoms (4.9%, n = 10). Most patients (74.5%, n = 152) had prior exposure to biologic therapy; most also presented with high or moderate disease activity (84.6%, n = 132). Treatment persistence at week 104 was 78.6% (n = 158), and the Kaplan-Meier estimate was 0.800 (95% confidence interval 0.736-0.850). Disease activity progressively improved. At week 104, 45.3% (n = 72) of patients had low disease activity, and 25.2% (n = 40) were in remission; 34.1% (n = 31) achieved very low disease activity, and, among patients with axial involvement, 61.9% (n = 26) had inactive or mild disease.

conclusionIxekizumab showed high 2-year treatment persistence and effectiveness in the treatment of patients with PsA and complex disease profiles, supporting its value in informing treatment decisions and optimising patient outcomes.

Indexed as

IxekizumabLong-term effectivenessPsoriatic arthritisReal-world evidenceTreatment persistence

Identifiers

PMID43007639

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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.