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Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results

OBJECTIVES: To evaluate 6-month effectiveness of ustekinumab versus tumour necrosis factor inhibitor (TNFi), analysing predictors of low disease activity (LDA)/remission. METHODS: PsABio is a prospective, observational cohort study of patients with psoriatic arthritis (PsA) at 92 sites in eight Euro...

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Autores principales: Smolen, Josef S, Siebert, Stefan, Korotaeva, Tatiana V, Selmi, Carlo, Bergmans, Paul, Gremese, Elisa, Joven-Ibáñez, Beatriz, Katsifis, Gkikas, Noël, Wim, Nurmohamed, Michael T, Richette, Pascal, Sfikakis, Petros P, de Vlam, Kurt, Theander, Elke, Gossec, Laure
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522461/
https://www.ncbi.nlm.nih.gov/pubmed/34162594
http://dx.doi.org/10.1136/annrheumdis-2021-220263
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author Smolen, Josef S
Siebert, Stefan
Korotaeva, Tatiana V
Selmi, Carlo
Bergmans, Paul
Gremese, Elisa
Joven-Ibáñez, Beatriz
Katsifis, Gkikas
Noël, Wim
Nurmohamed, Michael T
Richette, Pascal
Sfikakis, Petros P
de Vlam, Kurt
Theander, Elke
Gossec, Laure
author_facet Smolen, Josef S
Siebert, Stefan
Korotaeva, Tatiana V
Selmi, Carlo
Bergmans, Paul
Gremese, Elisa
Joven-Ibáñez, Beatriz
Katsifis, Gkikas
Noël, Wim
Nurmohamed, Michael T
Richette, Pascal
Sfikakis, Petros P
de Vlam, Kurt
Theander, Elke
Gossec, Laure
author_sort Smolen, Josef S
collection PubMed
description OBJECTIVES: To evaluate 6-month effectiveness of ustekinumab versus tumour necrosis factor inhibitor (TNFi), analysing predictors of low disease activity (LDA)/remission. METHODS: PsABio is a prospective, observational cohort study of patients with psoriatic arthritis (PsA) at 92 sites in eight European countries, who received first-line to third-line ustekinumab or a TNFi. Comparative achievement at 6 months of clinical Disease Activity Index for Psoriatic Arthritis (cDAPSA) LDA/remission, and minimal disease activity (MDA)/very LDA using propensity score (PS)-adjusted multivariate logistic regression was assessed. RESULTS: In the final analysis set of 868 participants with 6-month follow-up data (ustekinumab, n=426; TNFi, n=442), with long-standing disease and a high mean cDAPSA score (31.0 vs 29.8, respectively), proportions of patients in ustekinumab/TNFi treatment groups achieving cDAPSA LDA at 6 months were 45.7%/50.7%. cDAPSA remission was achieved in 14.9%/19.2%, and MDA in 26.4%/30.8% of patients. PS-adjusted odds ratios (OR; 95% confidence interval (CI)) of reaching cDAPSA LDA and MDA were 0.73 (0.46 to 1.15) and 0.87 (0.61 to 1.25) with ustekinumab versus TNFi, indicating no significant difference. High baseline body mass index or high cDAPSA were associated with a lower chance (OR (95% CI)) of reaching cDAPSA LDA with TNFi (0.94 (0.89 to 0.99) and 0.64 (0.52 to 0.79), respectively). Predictive factors were similar to previously published evidence, with cDAPSA and 12-item Psoriatic Arthritis Impact of Disease scores and chronic widespread pain at baseline appearing as new risk factors for unfavourable outcome. Safety data were similar between groups. CONCLUSION: Treatment targets were reached similarly after 6 months of treatment with ustekinumab and TNFi.
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spelling pubmed-85224612021-10-29 Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results Smolen, Josef S Siebert, Stefan Korotaeva, Tatiana V Selmi, Carlo Bergmans, Paul Gremese, Elisa Joven-Ibáñez, Beatriz Katsifis, Gkikas Noël, Wim Nurmohamed, Michael T Richette, Pascal Sfikakis, Petros P de Vlam, Kurt Theander, Elke Gossec, Laure Ann Rheum Dis Psoriatic Arthritis OBJECTIVES: To evaluate 6-month effectiveness of ustekinumab versus tumour necrosis factor inhibitor (TNFi), analysing predictors of low disease activity (LDA)/remission. METHODS: PsABio is a prospective, observational cohort study of patients with psoriatic arthritis (PsA) at 92 sites in eight European countries, who received first-line to third-line ustekinumab or a TNFi. Comparative achievement at 6 months of clinical Disease Activity Index for Psoriatic Arthritis (cDAPSA) LDA/remission, and minimal disease activity (MDA)/very LDA using propensity score (PS)-adjusted multivariate logistic regression was assessed. RESULTS: In the final analysis set of 868 participants with 6-month follow-up data (ustekinumab, n=426; TNFi, n=442), with long-standing disease and a high mean cDAPSA score (31.0 vs 29.8, respectively), proportions of patients in ustekinumab/TNFi treatment groups achieving cDAPSA LDA at 6 months were 45.7%/50.7%. cDAPSA remission was achieved in 14.9%/19.2%, and MDA in 26.4%/30.8% of patients. PS-adjusted odds ratios (OR; 95% confidence interval (CI)) of reaching cDAPSA LDA and MDA were 0.73 (0.46 to 1.15) and 0.87 (0.61 to 1.25) with ustekinumab versus TNFi, indicating no significant difference. High baseline body mass index or high cDAPSA were associated with a lower chance (OR (95% CI)) of reaching cDAPSA LDA with TNFi (0.94 (0.89 to 0.99) and 0.64 (0.52 to 0.79), respectively). Predictive factors were similar to previously published evidence, with cDAPSA and 12-item Psoriatic Arthritis Impact of Disease scores and chronic widespread pain at baseline appearing as new risk factors for unfavourable outcome. Safety data were similar between groups. CONCLUSION: Treatment targets were reached similarly after 6 months of treatment with ustekinumab and TNFi. BMJ Publishing Group 2021-11 2021-06-23 /pmc/articles/PMC8522461/ /pubmed/34162594 http://dx.doi.org/10.1136/annrheumdis-2021-220263 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Psoriatic Arthritis
Smolen, Josef S
Siebert, Stefan
Korotaeva, Tatiana V
Selmi, Carlo
Bergmans, Paul
Gremese, Elisa
Joven-Ibáñez, Beatriz
Katsifis, Gkikas
Noël, Wim
Nurmohamed, Michael T
Richette, Pascal
Sfikakis, Petros P
de Vlam, Kurt
Theander, Elke
Gossec, Laure
Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title_full Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title_fullStr Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title_full_unstemmed Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title_short Effectiveness of IL-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational PsABio study results
title_sort effectiveness of il-12/23 inhibition (ustekinumab) versus tumour necrosis factor inhibition in psoriatic arthritis: observational psabio study results
topic Psoriatic Arthritis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522461/
https://www.ncbi.nlm.nih.gov/pubmed/34162594
http://dx.doi.org/10.1136/annrheumdis-2021-220263
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