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Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52
INTRODUCTION: Improvements in both musculoskeletal and non-musculoskeletal manifestations are important treatment goals in psoriatic arthritis (PsA). OBJECTIVE: These post hoc analyses determined whether additional benefits related to various PsA domains are observed in patients simultaneously achie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599337/ https://www.ncbi.nlm.nih.gov/pubmed/34515902 http://dx.doi.org/10.1007/s10067-021-05891-5 |
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author | Behrens, Frank Leage, Soyi Liu Sapin, Christophe Baou, Celine El De La Torre, Inmaculada Meszaros, Gabriella Schett, Georg Combe, Bernard van den Bosch, Filip Gossec, Laure |
author_facet | Behrens, Frank Leage, Soyi Liu Sapin, Christophe Baou, Celine El De La Torre, Inmaculada Meszaros, Gabriella Schett, Georg Combe, Bernard van den Bosch, Filip Gossec, Laure |
author_sort | Behrens, Frank |
collection | PubMed |
description | INTRODUCTION: Improvements in both musculoskeletal and non-musculoskeletal manifestations are important treatment goals in psoriatic arthritis (PsA). OBJECTIVE: These post hoc analyses determined whether additional benefits related to various PsA domains are observed in patients simultaneously achieving 50% improvement in American College of Rheumatology criteria (ACR50) and 100% improvement in Psoriasis Area Severity Index (PASI100), the primary endpoint of the SPIRIT-H2H study. METHODS: Patients with active PsA and psoriasis in SPIRIT-H2H (N = 566) were categorised into two sets of four response groups irrespective of treatment allocation (approved dosages of ixekizumab or adalimumab): patients who simultaneously achieved ACR50 and PASI100 response, achieved ACR50 response only, achieved PASI100 response only, or did not achieve ACR50 or PASI100 response after 24 and 52 weeks of treatment. Patients achieving simultaneous ACR50 and PASI100 response were compared with the other patient response groups at the corresponding time point for efficacy and health-related quality of life (HRQoL) outcomes. RESULTS: Patients simultaneously achieving ACR50 and PASI100 responses at week 24 or 52 showed higher rates of ACR70 response, minimal disease activity, Disease Activity in Psoriatic Arthritis ≤ 4, resolution of enthesitis and dactylitis, and HRQoL improvement at weeks 24 and 52, respectively, than the other corresponding response groups at both time points. CONCLUSION: High levels of disease control, such as those obtained with simultaneous achievement of ACR50 and PASI100 response, were linked to better outcomes across a wide range of endpoints that are important for patients with PsA. Patients meeting this combined endpoint showed more comprehensive and thus greater control of disease activity. Trial registration NCT03151551 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10067-021-05891-5. |
format | Online Article Text |
id | pubmed-8599337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-85993372021-11-24 Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 Behrens, Frank Leage, Soyi Liu Sapin, Christophe Baou, Celine El De La Torre, Inmaculada Meszaros, Gabriella Schett, Georg Combe, Bernard van den Bosch, Filip Gossec, Laure Clin Rheumatol Original Article INTRODUCTION: Improvements in both musculoskeletal and non-musculoskeletal manifestations are important treatment goals in psoriatic arthritis (PsA). OBJECTIVE: These post hoc analyses determined whether additional benefits related to various PsA domains are observed in patients simultaneously achieving 50% improvement in American College of Rheumatology criteria (ACR50) and 100% improvement in Psoriasis Area Severity Index (PASI100), the primary endpoint of the SPIRIT-H2H study. METHODS: Patients with active PsA and psoriasis in SPIRIT-H2H (N = 566) were categorised into two sets of four response groups irrespective of treatment allocation (approved dosages of ixekizumab or adalimumab): patients who simultaneously achieved ACR50 and PASI100 response, achieved ACR50 response only, achieved PASI100 response only, or did not achieve ACR50 or PASI100 response after 24 and 52 weeks of treatment. Patients achieving simultaneous ACR50 and PASI100 response were compared with the other patient response groups at the corresponding time point for efficacy and health-related quality of life (HRQoL) outcomes. RESULTS: Patients simultaneously achieving ACR50 and PASI100 responses at week 24 or 52 showed higher rates of ACR70 response, minimal disease activity, Disease Activity in Psoriatic Arthritis ≤ 4, resolution of enthesitis and dactylitis, and HRQoL improvement at weeks 24 and 52, respectively, than the other corresponding response groups at both time points. CONCLUSION: High levels of disease control, such as those obtained with simultaneous achievement of ACR50 and PASI100 response, were linked to better outcomes across a wide range of endpoints that are important for patients with PsA. Patients meeting this combined endpoint showed more comprehensive and thus greater control of disease activity. Trial registration NCT03151551 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10067-021-05891-5. Springer International Publishing 2021-09-13 2021 /pmc/articles/PMC8599337/ /pubmed/34515902 http://dx.doi.org/10.1007/s10067-021-05891-5 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Behrens, Frank Leage, Soyi Liu Sapin, Christophe Baou, Celine El De La Torre, Inmaculada Meszaros, Gabriella Schett, Georg Combe, Bernard van den Bosch, Filip Gossec, Laure Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title | Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title_full | Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title_fullStr | Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title_full_unstemmed | Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title_short | Measuring treatment effect on psoriatic arthritis-related domains: insights from the SPIRIT-H2H study at weeks 24 and 52 |
title_sort | measuring treatment effect on psoriatic arthritis-related domains: insights from the spirit-h2h study at weeks 24 and 52 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8599337/ https://www.ncbi.nlm.nih.gov/pubmed/34515902 http://dx.doi.org/10.1007/s10067-021-05891-5 |
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