Evidence map›Paper›PMID 42523870›Full record

ArticleFrontiers in medicine2026

Real-life experience of tildrakizumab 200 mg in complex psoriatic patients: a case series.

Giulia Odorici, Cinzia Buligan, Carolina Fantini, Lucia Mantovani, Giulia Rech, Lidia Sacchelli

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In one paragraph

Article in Frontiers in medicine, 2026. 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
–field-weighted citation impact
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.

Giulia OdoriciSection of Dermatology and Infectious Diseases, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Cinzia BuliganInstitute of Dermatology, Azienda Sanitaria Universitaria Friuli Centrale (ASUFC), Udine, Italy.
Carolina FantiniSection of Dermatology, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Lucia MantovaniSection of Dermatology and Infectious Diseases, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Giulia RechDivision of Dermatology, Psoriasis Outpatient Service, APSS, Trento, Italy.
Lidia SacchelliDermatology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objectives: The management of moderate-to-severe plaque psoriasis may be particularly challenging in patients with a high disease burden and multiple comorbidities. This case series provides real-world evidence on the effectiveness of tildrakizumab 200 mg in patients with moderate-to-severe psoriasis characterized by clinical factors such as multiple comorbidities, high body weight, involvement of difficult-to-treat areas, and prior therapeutic failures. Methods: We present a series of six clinical cases describing baseline characteristics, treatment history and outcomes of patients with moderate-to-severe psoriasis treated with tildrakizumab 200 mg. Results: Although most of the patients included in this report showed multiple chronic or acute comorbidities (mainly cardiometabolic), high body weight, involvement of difficult-to-treat areas and failure to previous treatments (including biologics), tildrakizumab induced mostly complete remissions with most patients achieving PASI90 or PASI100 responses within 4-12 weeks; complete clearance (PASI100) was observed in four out of six patients. Treatment effectiveness was maintained over a follow-up of approximately 24 months in most cases, with a favorable safety profile. Conclusions: Tildrakizumab 200 mg demonstrated high effectiveness and sustained clinical responses in patients with moderate-to-severe psoriasis characterized by high disease burden and multiple comorbidities in a real-world setting.

Indexed as

biologicscomorbiditiesdifficult-to-treatmulti-failureobeseoverweightpsoriasistildrakizumab

Identifiers

PMID42523870
PMCPMC13408030

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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.