Evidence map›Paper›PMID 35384168›Full record

ArticleDermatologic therapy2022

Tildrakizumab in moderate-to-severe plaque psoriasis: A multicenter, retrospective, real-life study.

Giacomo Caldarola, Marco Galluzzo, Nicoletta Bernardini, Laura Calabrese, Marta Grimaldi, Gaia Moretta, Gianluca Pagnanelli, Ruslana Gaeta Shumak, Marina Talamonti, Lorenzo Tofani and 5 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Dermatologic therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 28 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

15 authors at 4 institutions in 1 country.

Giacomo CaldarolaDermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome.ORCID 0000-0002-8837-9232
Marco GalluzzoDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0002-3424-5175
Nicoletta BernardiniDepartment of Medical-Surgical Sciences and Biotechnologies, Dermatology Unit "Daniele Innocenzi", Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-6295-3574
Laura CalabreseDermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome.
Marta GrimaldiDermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome.
Gaia MorettaIstituto Dermopatico dell'Immacolata - IRCCS, Rome, Italy.ORCID 0000-0002-8839-5961
Gianluca PagnanelliIstituto Dermopatico dell'Immacolata - IRCCS, Rome, Italy.
Ruslana Gaeta ShumakDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Marina TalamontiDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Lorenzo TofaniDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.
Sabatino PallottaIstituto Dermopatico dell'Immacolata - IRCCS, Rome, Italy.
Ketty PerisDermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome.
Concetta PotenzaDepartment of Medical-Surgical Sciences and Biotechnologies, Dermatology Unit "Daniele Innocenzi", Sapienza University of Rome, Rome, Italy.
Clara De SimoneDermatologia, Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, Rome.
Elena CampioneDepartment of Systems Medicine, University of Rome "Tor Vergata", Rome, Italy.ORCID 0000-0001-7447-6798
Università Cattolica del Sacro Cuore · ITUniversity of Rome Tor Vergata · ITIstituto Dermopatico dell'Immacolata · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New biologic agents targeting interleukin (IL)23/T-helper17 axis, such as tildrakizumab, have been developed for the treatment of plaque psoriasis. To analyze the efficacy and safety of tildrakizumab in a real life setting of patients affected by moderate-to-severe psoriasis over a 28-week treatment period. A multicentric retrospective study was conducted in patients who initiated tildrakizumab between February 2020 and March 2021. Psoriasis Area and Severity Index-PASI was measured at baseline and after 4, 16 and 28 weeks. The percentage change in PASI value from baseline to the considered time-points, proportion of patients with absolute PASI <3 at week 28 and the percentages of achieving a PASI75 or PASI90 response were assessed. Data about potential safety issues and adverse events (AEs) were collected. Statistical analysis were performed for establish clinical efficacy and for variables predicting clinical response. Fifty nine patients with psoriasis were included. Overall mean PASI percentage reduction was of 88% from baseline to week 28 and 47 out of 59 patients (79.7%) at week 28 had an absolute PASI <3. PASI75 and PASI90 responses at week 28 were achieved by 48 (81.40%) patients and 38 (64.4.0%) patients, respectively. No substantial associations between gender, body mass index - BMI, PASI at baseline and prior exposition to biological therapies and the efficacy endpoints were retrieved. No serious safety issues or discontinuations related to adverse events were reported. In our real-life study, tildrakizumab showed high efficacy and a favorable safety profile, regardless of patient- and disease-related factors.

Indexed as

PsoriasisAntibodies, Monoclonal, HumanizedDouble-Blind MethodHumansInterleukin-23Retrospective StudiesSeverity of Illness IndexTreatment OutcomeAntibodies, Monoclonal, HumanizedInterleukin-23tildrakizumabefficacyinterleukin-23psoriasisreal-lifesafetytildrakizumab

Identifiers

PMID35384168
PMCPMC9287013
OpenAlexW4223474344

What OpenQuestion holds

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LicenceCC BY
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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.