Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study

Risankizumab is a humanized monoclonal antibody that binds the p19 subunit of interleukin-23. It is approved for treatment of moderate-severe chronic plaque psoriasis. This retrospective study included 66 consecutive adults with moderate-to-severe psoriasis vulgaris treated with risankizumab in mono...

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Autores principales: Riccardo G. Borroni, Piergiorgio Malagoli, Luigi Gargiulo, Mario Valenti, Giulia Pavia, Paola Facheris, Emanuela Morenghi, Isotta Giunipero di Corteranzo, Alessandra Narcisi, Michela Ortoncelli, Paolo Dapavo, Antonio Costanzo
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Publicado: Society for Publication of Acta Dermato-Venereologica 2021
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Acceso en línea:https://doaj.org/article/20c28872390140f28af22f527d4296d6
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spelling oai:doaj.org-article:20c28872390140f28af22f527d4296d62021-11-30T14:25:13ZReal-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study10.2340/actadv.v101.2830001-55551651-2057https://doaj.org/article/20c28872390140f28af22f527d4296d62021-11-01T00:00:00Zhttps://medicaljournalssweden.se/actadv/article/view/283https://doaj.org/toc/0001-5555https://doaj.org/toc/1651-2057Risankizumab is a humanized monoclonal antibody that binds the p19 subunit of interleukin-23. It is approved for treatment of moderate-severe chronic plaque psoriasis. This retrospective study included 66 consecutive adults with moderate-to-severe psoriasis vulgaris treated with risankizumab in monotherapy up to week 40 in a “real-life” setting. At week 40, 98.7%, 85.7% and 62.3% of patients achieved a Psoriasis Area and Severity Index (PASI) reduction ≥ 75% (PASI 75), PASI 90 and PASI 100, respectively. Patients who had not responded to 2 or more previous biologic treatments were significantly less likely to achieve PASI 75/90 at week 16 and PASI 90/100 at week 40 compared with those who had been previously treated with only 1 biologic, and compared with those treated with risankizumab as a first-line biologic. Increasing body mass index decreased the chances of reaching PASI 90 at week 40. No significant safety findings were recorded throughout the study, and none of the patients had to interrupt the treatment. These data suggest that the efficacy of risankizumab for plaque psoriasis in “real-life” clinical practice could differ from pivotal clinical trials data. Riccardo G. BorroniPiergiorgio MalagoliLuigi Gargiulo Mario ValentiGiulia PaviaPaola FacherisEmanuela MorenghiIsotta Giunipero di CorteranzoAlessandra NarcisiMichela OrtoncelliPaolo DapavoAntonio CostanzoSociety for Publication of Acta Dermato-Venereologicaarticlerisankizumabpsoriasisreal-lifeDermatologyRL1-803ENActa Dermato-Venereologica, Vol 101, Iss 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic risankizumab
psoriasis
real-life
Dermatology
RL1-803
spellingShingle risankizumab
psoriasis
real-life
Dermatology
RL1-803
Riccardo G. Borroni
Piergiorgio Malagoli
Luigi Gargiulo
Mario Valenti
Giulia Pavia
Paola Facheris
Emanuela Morenghi
Isotta Giunipero di Corteranzo
Alessandra Narcisi
Michela Ortoncelli
Paolo Dapavo
Antonio Costanzo
Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
description Risankizumab is a humanized monoclonal antibody that binds the p19 subunit of interleukin-23. It is approved for treatment of moderate-severe chronic plaque psoriasis. This retrospective study included 66 consecutive adults with moderate-to-severe psoriasis vulgaris treated with risankizumab in monotherapy up to week 40 in a “real-life” setting. At week 40, 98.7%, 85.7% and 62.3% of patients achieved a Psoriasis Area and Severity Index (PASI) reduction ≥ 75% (PASI 75), PASI 90 and PASI 100, respectively. Patients who had not responded to 2 or more previous biologic treatments were significantly less likely to achieve PASI 75/90 at week 16 and PASI 90/100 at week 40 compared with those who had been previously treated with only 1 biologic, and compared with those treated with risankizumab as a first-line biologic. Increasing body mass index decreased the chances of reaching PASI 90 at week 40. No significant safety findings were recorded throughout the study, and none of the patients had to interrupt the treatment. These data suggest that the efficacy of risankizumab for plaque psoriasis in “real-life” clinical practice could differ from pivotal clinical trials data.
format article
author Riccardo G. Borroni
Piergiorgio Malagoli
Luigi Gargiulo
Mario Valenti
Giulia Pavia
Paola Facheris
Emanuela Morenghi
Isotta Giunipero di Corteranzo
Alessandra Narcisi
Michela Ortoncelli
Paolo Dapavo
Antonio Costanzo
author_facet Riccardo G. Borroni
Piergiorgio Malagoli
Luigi Gargiulo
Mario Valenti
Giulia Pavia
Paola Facheris
Emanuela Morenghi
Isotta Giunipero di Corteranzo
Alessandra Narcisi
Michela Ortoncelli
Paolo Dapavo
Antonio Costanzo
author_sort Riccardo G. Borroni
title Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
title_short Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
title_full Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
title_fullStr Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
title_full_unstemmed Real-life Effectiveness and Safety of Risankizumab in Moderate-to-severe Plaque Psoriasis: A 40-week Multicentric Retrospective Study
title_sort real-life effectiveness and safety of risankizumab in moderate-to-severe plaque psoriasis: a 40-week multicentric retrospective study
publisher Society for Publication of Acta Dermato-Venereologica
publishDate 2021
url https://doaj.org/article/20c28872390140f28af22f527d4296d6
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