Performance and Predictors of Minimal Disease Activity Response in Patients With Peripheral Spondyloarthritis Treated With Adalimumab

Objective To examine the concurrent validity and discrimination of criteria for modified minimal disease activity (MDA) in peripheral spondyloarthritis (SpA) following filter principles of Outcome Measures in Rheumatology (OMERACT) and to determine predictors of modified MDA response. Methods Four m...

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Veröffentlicht in:Arthritis care & research (2010) 2022-02, Vol.74 (2), p.259-267
Hauptverfasser: Coates, Laura C., Abraham, Sonya, Tillett, William, Mease, Philip J., Ramiro, Sofia, Wu, Tianshuang, Wang, Xin, Pangan, Aileen L., Song, In‐Ho
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container_issue 2
container_start_page 259
container_title Arthritis care & research (2010)
container_volume 74
creator Coates, Laura C.
Abraham, Sonya
Tillett, William
Mease, Philip J.
Ramiro, Sofia
Wu, Tianshuang
Wang, Xin
Pangan, Aileen L.
Song, In‐Ho
description Objective To examine the concurrent validity and discrimination of criteria for modified minimal disease activity (MDA) in peripheral spondyloarthritis (SpA) following filter principles of Outcome Measures in Rheumatology (OMERACT) and to determine predictors of modified MDA response. Methods Four modified MDA versions were derived in the ABILITY‐2 study using the Spondyloarthritis Research Consortium of Canada (SPARCC) enthesitis index or the Leeds Enthesitis Index (LEI) while excluding psoriasis. To assess concurrent validity, modified MDA versions were correlated with Peripheral Spondyloarthritis Response Criteria (PSpARC) remission, Ankylosing Spondylitis Disease Activity Score showing inactive disease (ASDAS ID), and physician global assessment of disease activity. Treatment discrimination was assessed between adalimumab and placebo at week 12. Multiple logistic regression was used to determine baseline predictors of long‐term modified MDA responses and sustained modified MDA. Results The 4 modified MDA versions showed a stronger positive correlation with PSpARC remission (rtet > 0.95) versus ASDAS ID (rtet > 0.75) at week 12 and years 1–3 and were able to show discrimination (P 
doi_str_mv 10.1002/acr.24442
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Methods Four modified MDA versions were derived in the ABILITY‐2 study using the Spondyloarthritis Research Consortium of Canada (SPARCC) enthesitis index or the Leeds Enthesitis Index (LEI) while excluding psoriasis. To assess concurrent validity, modified MDA versions were correlated with Peripheral Spondyloarthritis Response Criteria (PSpARC) remission, Ankylosing Spondylitis Disease Activity Score showing inactive disease (ASDAS ID), and physician global assessment of disease activity. Treatment discrimination was assessed between adalimumab and placebo at week 12. Multiple logistic regression was used to determine baseline predictors of long‐term modified MDA responses and sustained modified MDA. Results The 4 modified MDA versions showed a stronger positive correlation with PSpARC remission (rtet &gt; 0.95) versus ASDAS ID (rtet &gt; 0.75) at week 12 and years 1–3 and were able to show discrimination (P &lt; 0.001). Responsiveness was shown at week 12; significantly more patients receiving adalimumab versus placebo achieved all 4 versions of modified MDA. Approximately 40–60% of patients treated with adalimumab achieved modified MDA using the LEI or SPARCC enthesitis index at years 1–3. Achieving modified MDA response after 12 weeks of adalimumab treatment was a robust positive predictor of attaining long‐term modified MDA through 3 years (odds ratio [OR] 11.38–27.13 for modified MDA using the LEI; OR 17.98–37.85 for modified MDA using the SPARCC enthesitis index). Conclusion All 4 versions of modified MDA showed concurrent validity and discriminated well between adalimumab and placebo treatment groups. Early modified MDA response is a more consistent predictor of long‐term modified MDA achievement than baseline characteristics. The 5 of 6 versions of modified MDA could be an appropriate treatment target in patients with peripheral SpA.</description><identifier>ISSN: 2151-464X</identifier><identifier>EISSN: 2151-4658</identifier><identifier>DOI: 10.1002/acr.24442</identifier><identifier>PMID: 32937016</identifier><language>eng</language><publisher>Boston, USA: Wiley Periodicals, Inc</publisher><subject>Adalimumab - therapeutic use ; Ankylosing spondylitis ; Antirheumatic Agents - therapeutic use ; Arthritis ; Discrimination ; Double-Blind Method ; Humans ; Inflammatory diseases ; Monoclonal antibodies ; Outcome Assessment, Health Care ; Patients ; Placebos ; Psoriasis ; Remission ; Remission (Medicine) ; Rheumatic diseases ; Rheumatology ; Spondylarthritis - drug therapy ; TNF inhibitors ; Validity</subject><ispartof>Arthritis care &amp; research (2010), 2022-02, Vol.74 (2), p.259-267</ispartof><rights>2020 The Authors. published by Wiley Periodicals LLC on behalf of American College of Rheumatology.</rights><rights>2020 The Authors. Arthritis Care &amp; Research published by Wiley Periodicals LLC on behalf of American College of Rheumatology.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). 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Methods Four modified MDA versions were derived in the ABILITY‐2 study using the Spondyloarthritis Research Consortium of Canada (SPARCC) enthesitis index or the Leeds Enthesitis Index (LEI) while excluding psoriasis. To assess concurrent validity, modified MDA versions were correlated with Peripheral Spondyloarthritis Response Criteria (PSpARC) remission, Ankylosing Spondylitis Disease Activity Score showing inactive disease (ASDAS ID), and physician global assessment of disease activity. Treatment discrimination was assessed between adalimumab and placebo at week 12. Multiple logistic regression was used to determine baseline predictors of long‐term modified MDA responses and sustained modified MDA. Results The 4 modified MDA versions showed a stronger positive correlation with PSpARC remission (rtet &gt; 0.95) versus ASDAS ID (rtet &gt; 0.75) at week 12 and years 1–3 and were able to show discrimination (P &lt; 0.001). Responsiveness was shown at week 12; significantly more patients receiving adalimumab versus placebo achieved all 4 versions of modified MDA. Approximately 40–60% of patients treated with adalimumab achieved modified MDA using the LEI or SPARCC enthesitis index at years 1–3. Achieving modified MDA response after 12 weeks of adalimumab treatment was a robust positive predictor of attaining long‐term modified MDA through 3 years (odds ratio [OR] 11.38–27.13 for modified MDA using the LEI; OR 17.98–37.85 for modified MDA using the SPARCC enthesitis index). Conclusion All 4 versions of modified MDA showed concurrent validity and discriminated well between adalimumab and placebo treatment groups. Early modified MDA response is a more consistent predictor of long‐term modified MDA achievement than baseline characteristics. 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Abraham, Sonya ; Tillett, William ; Mease, Philip J. ; Ramiro, Sofia ; Wu, Tianshuang ; Wang, Xin ; Pangan, Aileen L. ; Song, In‐Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3882-127f677b44500a16a7e5c63443832484f06349f3a3f1fe725006078b68b2acee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adalimumab - therapeutic use</topic><topic>Ankylosing spondylitis</topic><topic>Antirheumatic Agents - therapeutic use</topic><topic>Arthritis</topic><topic>Discrimination</topic><topic>Double-Blind Method</topic><topic>Humans</topic><topic>Inflammatory diseases</topic><topic>Monoclonal antibodies</topic><topic>Outcome Assessment, Health Care</topic><topic>Patients</topic><topic>Placebos</topic><topic>Psoriasis</topic><topic>Remission</topic><topic>Remission (Medicine)</topic><topic>Rheumatic diseases</topic><topic>Rheumatology</topic><topic>Spondylarthritis - drug therapy</topic><topic>TNF inhibitors</topic><topic>Validity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Coates, Laura C.</creatorcontrib><creatorcontrib>Abraham, Sonya</creatorcontrib><creatorcontrib>Tillett, William</creatorcontrib><creatorcontrib>Mease, Philip J.</creatorcontrib><creatorcontrib>Ramiro, Sofia</creatorcontrib><creatorcontrib>Wu, Tianshuang</creatorcontrib><creatorcontrib>Wang, Xin</creatorcontrib><creatorcontrib>Pangan, Aileen L.</creatorcontrib><creatorcontrib>Song, In‐Ho</creatorcontrib><collection>Wiley Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis care &amp; research (2010)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Coates, Laura C.</au><au>Abraham, Sonya</au><au>Tillett, William</au><au>Mease, Philip J.</au><au>Ramiro, Sofia</au><au>Wu, Tianshuang</au><au>Wang, Xin</au><au>Pangan, Aileen L.</au><au>Song, In‐Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Performance and Predictors of Minimal Disease Activity Response in Patients With Peripheral Spondyloarthritis Treated With Adalimumab</atitle><jtitle>Arthritis care &amp; research (2010)</jtitle><addtitle>Arthritis Care Res (Hoboken)</addtitle><date>2022-02</date><risdate>2022</risdate><volume>74</volume><issue>2</issue><spage>259</spage><epage>267</epage><pages>259-267</pages><issn>2151-464X</issn><eissn>2151-4658</eissn><abstract>Objective To examine the concurrent validity and discrimination of criteria for modified minimal disease activity (MDA) in peripheral spondyloarthritis (SpA) following filter principles of Outcome Measures in Rheumatology (OMERACT) and to determine predictors of modified MDA response. Methods Four modified MDA versions were derived in the ABILITY‐2 study using the Spondyloarthritis Research Consortium of Canada (SPARCC) enthesitis index or the Leeds Enthesitis Index (LEI) while excluding psoriasis. To assess concurrent validity, modified MDA versions were correlated with Peripheral Spondyloarthritis Response Criteria (PSpARC) remission, Ankylosing Spondylitis Disease Activity Score showing inactive disease (ASDAS ID), and physician global assessment of disease activity. Treatment discrimination was assessed between adalimumab and placebo at week 12. Multiple logistic regression was used to determine baseline predictors of long‐term modified MDA responses and sustained modified MDA. Results The 4 modified MDA versions showed a stronger positive correlation with PSpARC remission (rtet &gt; 0.95) versus ASDAS ID (rtet &gt; 0.75) at week 12 and years 1–3 and were able to show discrimination (P &lt; 0.001). Responsiveness was shown at week 12; significantly more patients receiving adalimumab versus placebo achieved all 4 versions of modified MDA. Approximately 40–60% of patients treated with adalimumab achieved modified MDA using the LEI or SPARCC enthesitis index at years 1–3. Achieving modified MDA response after 12 weeks of adalimumab treatment was a robust positive predictor of attaining long‐term modified MDA through 3 years (odds ratio [OR] 11.38–27.13 for modified MDA using the LEI; OR 17.98–37.85 for modified MDA using the SPARCC enthesitis index). Conclusion All 4 versions of modified MDA showed concurrent validity and discriminated well between adalimumab and placebo treatment groups. Early modified MDA response is a more consistent predictor of long‐term modified MDA achievement than baseline characteristics. The 5 of 6 versions of modified MDA could be an appropriate treatment target in patients with peripheral SpA.</abstract><cop>Boston, USA</cop><pub>Wiley Periodicals, Inc</pub><pmid>32937016</pmid><doi>10.1002/acr.24442</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6620-0457</orcidid><orcidid>https://orcid.org/0000-0002-4756-663X</orcidid><orcidid>https://orcid.org/0000-0002-8899-9087</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adalimumab - therapeutic use
Ankylosing spondylitis
Antirheumatic Agents - therapeutic use
Arthritis
Discrimination
Double-Blind Method
Humans
Inflammatory diseases
Monoclonal antibodies
Outcome Assessment, Health Care
Patients
Placebos
Psoriasis
Remission
Remission (Medicine)
Rheumatic diseases
Rheumatology
Spondylarthritis - drug therapy
TNF inhibitors
Validity
title Performance and Predictors of Minimal Disease Activity Response in Patients With Peripheral Spondyloarthritis Treated With Adalimumab
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