Evidence map›Paper›PMID 36063283›Full record

ArticleDermatology and therapy2022

Real-Life Effectiveness and Safety of Risankizumab in 131 Patients Affected by Moderate-to-Severe Plaque Psoriasis: A 52-Week Retrospective Study.

Luigi Gargiulo, Luciano Ibba, Giulia Pavia, Carlo Alberto Vignoli, Francesco Piscazzi, Mario Valenti, Federica Sanna, Chiara Perugini, Jessica Avagliano, Antonio Costanzo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Dermatology and therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Luigi GargiuloDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy. luciano.ibba@humanitas.it.
Luciano IbbaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.ORCID http://orcid.org/0000-0002-7876-4866
Giulia PaviaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.
Carlo Alberto VignoliDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.
Francesco PiscazziDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.
Mario ValentiDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.
Federica SannaDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
Chiara PeruginiDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
Jessica AvaglianoDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
Antonio CostanzoDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, MI, Italy.
Alessandra NarcisiDermatology Unit, IRCCS Humanitas Research Hospital, Rozzano, MI, Italy.
Humanitas University · ITIRCCS Humanitas Research Hospital · IT

Funding

Ministero della Salute CO-2013-02356463
6 · The paper itself

Abstract

introductionRisankizumab is a humanized monoclonal antibody that selectively targets interleukin-23. It is approved for treatment of moderate-to-severe plaque psoriasis. We conducted a 52-week monocentric retrospective study to evaluate the effectiveness and safety of risankizumab in a real-life setting.

methodsOur study included 131 adults with moderate-to-severe plaque psoriasis all treated with risankizumab for at least 52 weeks. Patient characteristics and PASI (Psoriasis Area and Severity Index) at each visit were recorded. The percentages of patients achieving 75%/90%/100% (PASI 75/90/100) improvement in PASI with respect to baseline were registered.

resultsAt week 52, 93.9%, 78.6%, and 61.1% of patients achieved PASI 75/90/100, respectively. An absolute PASI ≤ 2 was reached by 90.8% at week 52. The higher body mass index and the presence of cardio-metabolic comorbidities did not interfere with the odds of reaching PASI 75/90/100 at each time-point. At week 52, comparable percentages of patients achieved PASI 100, regardless of the involvement of difficult-to-treat-areas. No significant safety findings were recorded and none of the patients had to interrupt the treatment because of adverse events.

conclusionsOur findings confirmed that risankizumab is a safe and effective therapeutic option for the treatment of a wide "real-life" cohort of patients with psoriasis.

Indexed as

Anti-IL-23BiologicsPsoriasisReal-lifeRisankizumab

Identifiers

PMID36063283
PMCPMC9443623
OpenAlexW4294622315

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.