Evidence map›Paper›PMID 36156312›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2023

Real-life effectiveness of tildrakizumab in chronic plaque psoriasis: A 52-week multicentre retrospective study-IL PSO (Italian landscape psoriasis).

Alessandra Narcisi, Mario Valenti, Luigi Gargiulo, Luciano Ibba, Fabrizio Amoruso, Giuseppe Argenziano, Federico Bardazzi, Martina Burlando, Carlo Giovanni Carrera, Giovanni Damiani and 10 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.3field-weighted citation impact, top 6% of its field
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

33 citing papers in PubMed, 41 citations in OpenAlex.

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  7. IL-23 Inhibitors in Psoriasis: What Have We Learnt so Far?Journal of inflammation research · 2026
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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

20 authors at 15 institutions in 1 country.

Alessandra NarcisiDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.
Mario ValentiDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.ORCID https://orcid.org/0000-0001-9140-9263
Luigi GargiuloDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.ORCID https://orcid.org/0000-0002-6051-1676
Luciano IbbaDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.ORCID https://orcid.org/0000-0002-7876-4866
Fabrizio AmorusoDermatology Unit, Azienda Ospedaliera di Cosenza, Cosenza, Italy.
Giuseppe ArgenzianoDepartment of Dermatology, 'Luigi Vanvitelli' University School of Medicine, Naples, Italy.ORCID https://orcid.org/0000-0003-1413-8214
Federico BardazziDermatology Unit, Department of Specialistic, Diagnostic and Experimental Medicine, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Martina BurlandoSection of Dermatology, Department of Health Sciences (DISSAL), IRCCS San Martino University Hospital, Genoa, Italy.ORCID https://orcid.org/0000-0002-4381-6718
Carlo Giovanni CarreraFondazione Cà Granda IRCCS Maggiore Policlinico Hospital, Milan, Italy.
Giovanni DamianiClinical Dermatology, I.R.C.C.S. Istituto Ortopedico Galeazzi, Milan, Italy.ORCID https://orcid.org/0000-0002-2390-6505
Paolo DapavoDepartment of Biomedical Science and Human Oncology, Second Dermatologic Clinic, University of Turin, Turin, Italy.
Valentina DiniDermatology Unit, Department of Clinical and Experimental Medicine Ospedale Santa Chiara, Pisa, Italy.ORCID https://orcid.org/0000-0002-8537-1999
Chiara FranchiClinical Dermatology, I.R.C.C.S. Istituto Ortopedico Galeazzi, Milan, Italy.
Giampiero GirolomoniDepartment of Medicine, Section of Dermatology and Venereology, University of Verona, Verona, Italy.ORCID https://orcid.org/0000-0001-8548-0493
Claudio GuarneriDepartment of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, Messina, Italy.
Francesco LoconsoleDepartment of Dermatology, University of Bari, Bari, Italy.
Francesca SampognaIstituto Dermopatico Dell'Immacolata, (IDI) IRCCS, Rome, Italy.ORCID https://orcid.org/0000-0002-7624-3290
Massimo TravagliniU.O.S.D. dermatologica - centro per la cura della psoriasi, Ospedale Perrino, Brindisi, Italy.
Piergiorgio MalagoliDepartment of Dermatology, Dermatology Unit Azienda Ospedaliera San Donato Milanese, Milan, Italy.
Antonio CostanzoDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano (MI), Italy.ORCID https://orcid.org/0000-0001-9697-2557
Humanitas University · ITIstituto Ortopedico Galeazzi · ITAzienda Ospedaliera di Cosenza · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITIRCCS Policlinico San Donato · ITIstituto Dermopatico dell'Immacolata · ITOspedale A. Perrino · ITOspedale Policlinico San Martino · ITOspedale Santa Chiara · ITUniversity of Bari Aldo Moro · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Messina · ITUniversity of Turin · ITUniversity of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTildrakizumab is a humanized monoclonal antibody that binds selectively the p19 subunit of interleukin-23. It is approved for treatment of moderate-severe chronic plaque psoriasis.

objectivesWe conducted a 52-week retrospective study to assess the effectiveness and safety of tildrakizumab in a real-life setting.

methodsOur retrospective study included 237 consecutive adults with moderate-to-severe plaque psoriasis, enrolled in 10 different Italian centres, treated with tildrakizumab up to Week 52. Patient characteristics, comorbidities, previous treatments and the PASI (Psoriasis Area and Severity Index) score at each visit (baseline, Week 16, Week 28 and Week 52) were retrieved from the electronic medical records. The percentages of patients achieving 75%, 90% and 100% (PASI 75, PASI 90 and PASI 100) improvement in PASI with respect to baseline PASI were registered.

resultsAt Week 52, 90.91%, 73.55% and 58.68% of patients achieved a PASI reduction ≥75% (PASI 75), PASI 90 and PASI 100, respectively. An absolute PASI ≤ 2 was reached by 85.95% at Week 52. Compared with Phase 3 clinical trials, we observed similar rates of PASI 75/90 responses and higher percentages of patients achieving PASI 100. Patients who had not responded to previous biologic treatments and patients with cardio-metabolic comorbidities were significantly more likely to achieve PASI 100 at Week 28 and PASI 90 at Week 52. The higher body mass index did not interfere with the odds of reaching PASI 75/90/100 at each time point. No significant safety findings were recorded throughout the study, and none of the patients had to interrupt the treatment because of adverse events.

conclusionOur data suggest that the efficacy of tildrakizumab for plaque psoriasis in 'real-life' clinical practice is comparable with Phase 3 clinical trials with higher percentages of patients achieving complete skin clearance (PASI 100) at Weeks 16, 28 and 52.

Indexed as

PsoriasisAdultAntibodies, Monoclonal, HumanizedHumansItalyRetrospective StudiesSeverity of Illness IndexTreatment OutcomeAntibodies, Monoclonal, Humanizedtildrakizumab

Identifiers

PMID36156312
PMCPMC10092064
OpenAlexW4297250253

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.