Evidence map›Paper›PMID 41236286›Full record

ArticleDermatology practical & conceptual2025

Long-Term Persistence with Guselkumab: A 5-Year Multicenter Retrospective Study across 14 Dermatology Centers in Italy.

Bernardini Nicoletta, Caldarola Giacomo, Richetta Antonio Giovanni, Esposito Maria, Trovato Federica, Amerio Paolo, Morea Edvige, Bonifati Claudio, Graceffa Dario, Bruni Pier Luigi and 17 more

Abstract read
In one paragraph

Article in Dermatology practical & conceptual, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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

27 authors.

Bernardini NicolettaDermatology Unit, A. Fiorini Hospital, Sapienza University of Rome - Polo Pontino, Terracina, Italy.
Caldarola GiacomoSection of Dermatology, Department of Translational Medicine and Surgery, Catholic University of the S. Heart, Rome, Italy.
Richetta Antonio GiovanniDepartment of Internal Medicine and Medical Specialties, Sapienza University of Rome, Policlinico Umberto I, Rome, Italy.
Esposito MariaUnit of General and Oncologic Dermatology, San Salvatore Hospital, L'Aquila, Italy.
Trovato FedericaIDI-IRCCS, Luigi Maria Monti Foundation, Rome, Italy.
Amerio PaoloDermatology Unit, Local Health Authority ASL2 Abruzzo, Chieti, Italy.
Morea EdvigeDermatology Unit, Local Health Authority ASL2 Abruzzo, Chieti, Italy.
Bonifati ClaudioClinical Dermatology - Psoriasis Center, San Gallicano Dermatological Institute (IRCCS), Rome, Italy.
Graceffa DarioIFO-San Gallicano Hospital, Rome, Italy.
Bruni Pier LuigiDermatology Clinic, Terni, Italy.
Giordano DomenicoSant' Andrea Hospital, Department of Neurosciences, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Rome, Italy.
Persechino SeverinoSant' Andrea Hospital, Department of Neurosciences, Mental Health and Sensory Organs (NESMOS), Sapienza University of Rome, Rome, Italy.
Mazzotta AnnamariaDermatology Unit, San Camillo Forlanini Hospital, Rome, Italy.
Moretta GaiaIDI-IRCCS, Luigi Maria Monti Foundation, Rome, Italy.
Pagnanelli GianlucaIDI-IRCCS, Luigi Maria Monti Foundation, Rome, Italy.
Pallotta SabatinoIDI-IRCCS, Luigi Maria Monti Foundation, Rome, Italy.
Annedda JasmineDepartment of Medical Sciences and Public Health, Dermatology Clinic, University of Cagliari, Cagliari, Italy.
Mugheddu CristinaDepartment of Medical Sciences and Public Health, Dermatology Clinic, University of Cagliari, Cagliari, Italy.
Miraglia EmanueleSan Sebastiano Hospital, Frascati, Italy.
Panasiti VincenzoDermatology Unit, Campus Bio-Medico University Hospital, Rome, Italy.
Molinelli ElisaDermatology Clinic, Azienda Ospedaliero-Universitaria Ospedali Riuniti, Ancona, Italy.
Simonetti OrianaDermatology Clinic, Azienda Ospedaliero-Universitaria Ospedali Riuniti, Ancona, Italy.
Fargnoli Maria ConcettaUnit of General and Oncologic Dermatology, San Salvatore Hospital, L'Aquila, Italy.
Peris KettySection of Dermatology, Department of Translational Medicine and Surgery, Catholic University of the S. Heart, Rome, Italy.
Pellacani GiovanniDepartment of Internal Medicine and Medical Specialties, Sapienza University of Rome, Policlinico Umberto I, Rome, Italy.
Potenza ConcettaDermatology Unit, A. Fiorini Hospital, Sapienza University of Rome - Polo Pontino, Terracina, Italy.
Dattola AnnunziataDepartment of Internal Medicine and Medical Specialties, Sapienza University of Rome, Policlinico Umberto I, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPsoriasis is a chronic systemic inflammatory disease that requires long-term treatment strategies to maintain sustained disease control. Treatment persistence is an important real-world indicator of therapeutic effectiveness and tolerability. Guselkumab, an IL-23 inhibitor, has shown favorable persistence in several studies, but extended long-term data remain limited.

objectivesTo assess 3- and 5-year drug survival rates of guselkumab in patients with moderate-to-severe plaque psoriasis and to examine the relationship between persistence and clinical variables such as PASI, BMI, prior biologic exposure, and involvement of difficult-to-treat areas.

methodsThis was a multicenter retrospective observational study conducted across 14 dermatology centers in Italy. Adult patients with moderate-to-severe plaque psoriasis who started guselkumab were included. Data collected included demographics, clinical history, disease severity, comorbidities, and treatment details. Drug survival was analyzed using Kaplan-Meier curves and Cox proportional hazards models.

resultsA total of 247 patients were included. At three years, 80.2% of patients remained on guselkumab, and at five years, 72.8% continued treatment. Persistence was not significantly influenced by BMI, PASI, or age. However, prior biologics exposure was associated with a higher risk of discontinuation (hazard ratio (HR): 1.84; P=0.0208), especially in those previously treated with IL-17 inhibitors (HR:2.14; P=0.0150). The involvement of difficult-to-treat areas did not significantly affect persistence, although a trend toward reduced discontinuation was observed in patients with genital involvement (P=0.0539).

conclusionsGuselkumab demonstrated high long-term persistence in real-world clinical practice. Drug survival remained consistently high across various subgroups, with prior IL-17 inhibitor exposure being the main predictor of decreased persistence.

Identifiers

PMID41236286
PMCPMC12615130

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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 Socratic graph.