Evidence map›Paper›PMID 42029886›Full record

ArticleDermatology and therapy2026

Tildrakizumab Improves Disease Severity and Patient-Reported Outcomes in Moderate-to-Severe Chronic Plaque Psoriasis: A Prospective Real-World Study.

Paola Facheris, Francesco Piscazzi, Giovanni Fiorillo, Mario Valenti, Antonio Costanzo, Riccardo G Borroni

Abstract read
In one paragraph

Article in Dermatology 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

6 authors.

Paola FacherisDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy. Paola.facheris91@gmail.com.ORCID http://orcid.org/0000-0002-5171-9854
Francesco PiscazziDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy.ORCID http://orcid.org/0000-0001-9495-6350
Giovanni FiorilloDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy.ORCID http://orcid.org/0000-0002-3089-4362
Mario ValentiDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy.ORCID http://orcid.org/0000-0001-9140-9263
Antonio CostanzoDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy.ORCID http://orcid.org/0000-0001-9697-2557
Riccardo G BorroniDermatology Unit, Humanitas Research Hospital-IRCCS, Via Manzoni 56, 20089, Rozzano, MI, Italy.ORCID http://orcid.org/0000-0002-5704-1220

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionChronic plaque psoriasis significantly impairs physical, psychological, and social well-being. Patient-reported outcome measures (PROMs) are increasingly recognized as essential endpoints. Tildrakizumab, an interleukin (IL)-23p19 inhibitor, has demonstrated high efficacy and safety in clinical trials, but real-world data on its impact on PROMs remain limited. We aimed to evaluate the effect of tildrakizumab on psoriasis severity, symptoms, and health-related quality of life, including sleep disorders, and to assess correlations between severity of the disease (measured using the Psoriasis Area and Severity Index [PASI]) improvement and PROMs in a real-world cohort.

methodsConsecutive adults with moderate-to-severe plaque psoriasis initiating tildrakizumab were enrolled and prospectively followed for 52 weeks. Assessments at baseline, week 16, and week 52 included the PASI; Dermatology Life Quality Index (DLQI); Skindex-16; Visual Analog Scale (VAS) for pruritus, scaling, and pain; the Medical Outcomes Study Sleep Scale (MOS-Sleep); and Work Productivity and Activity Impairment (WPAI) questionnaire.

resultsThirty-three patients were enrolled in the study. Tildrakizumab induced rapid skin clearance and symptoms relief, with marked reductions in PASI and most PROMs by week 16. Pain and MOS-Sleep improved significantly only at Week 52. PASI correlated with PROMs at Week 16 (Spearman correlation), especially DLQI (r = 0.69, p < 0.001) and pruritus (r = 0.70, p < 0.001). At Week 52, correlations weakened for most PROMs, except Skindex-16 (r = 0.62, p < 0.01), pruritus (r = 0.54, p = 0.02), and scaling (r = 0.55, p = 0.02). Repeated-measures correlation analysis demonstrated significant within-subject associations between PASI improvement and most patient-reported outcomes (DLQI, scaling, pain, pruritus, and Skindex-16), while no significant associations were observed for WPAI and MOS-Sleep.

conclusionsTildrakizumab improves both objective disease severity and quality of life at week 16. PASI strongly correlates with PROM improvements early in treatment, but correlations diminish over time, suggesting possible adaptation once skin clearance is sustained. PROMs should be integrated into long-term management to capture patient-centered benefits beyond skin clearance.

Indexed as

DLQIMOS-SleepPROMsPsoriasisQuality of lifeSkindex-16SleepTildrakizumab

Identifiers

PMID42029886
PMCPMC13237329

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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.