ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "Response Criteria"

  • Abstract Number: 2110 • ACR Convergence 2022

    Guselkumab Efficacy in Psoriatic Arthritis Assessed by Multi-domain Composite Indices: Data from the Phase 3b COSMOS Trial in a TNFi-IR Population

    Laure Gossec1, Mohamed Sharaf2, Elke Theander3, Marlies Neuhold4, Paul Bergmans5, May Shawi6, Michelle Perate7, Christine Contré8 and Laura Coates9, 1Sorbonne Université, Paris, France, 2Johnson & Johnson, Middle East FZ LLC, Dubai, United Arab Emirates, 3Formerly at Janssen Scientific Affairs, LLC, Solna, Sweden, 4Takeda Europe & Canada Business Unit (EUCAN) Medical Affairs, Zurich, Switzerland; formerly at Janssen Scientific Affairs, LLC, Zug, Switzerland, 5Formerly at Janssen, Breda, Netherlands, 6Immunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson, Horsham, PA, 7Janssen Scientific Affairs, LLC, Horsham, PA, 8Formerly at Janssen Scientific Affairs, LLC, Issy-les-Moulineaux, France, Issy-les-Moulineaux, France, 9Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK, Oxford, England, United Kingdom

    Background/Purpose: The Phase 3b COSMOS study (NCT03796858) demonstrated the efficacy and safety of guselkumab (GUS), an IL-23 p19 subunit inhibitor, in patients (pts) with psoriatic…
  • Abstract Number: 0295 • ACR Convergence 2022

    Safety and Efficacy of Upadacitinib in Patients with Rheumatoid Arthritis and Inadequate Response to Conventional Synthetic DMARDs: Results Through 5 Years from the SELECT-NEXT Study

    Gerd Burmester1, Filip Van den bosch2, John Tesser3, Anna K Shmagel4, Yuanyuan Duan4, Nasser Khan5, Heidi Camp6 and Alan Kivitz7, 1Charité University Medicine Berlin, Berlin, Germany, 2Department of Internal Medicine and Paediatrics, Ghent University and VIB Centre for Inflammation Research, Ghent, Belgium, 3Arizona Arthritis & Rheumatology Associates, Phoenix, AZ, 4AbbVie, Inc., North Chicago, IL, 5AbbVie, Inc., Abbott Park, IL, 6Abbvie, Winnetka, IL, 7Department of Rheumatology, Altoona Center for Clinical Research, Duncansville, PA

    Background/Purpose: In the phase 3 SELECT-NEXT study, upadacitinib (UPA) demonstrated efficacy at wk 12 and sustained efficacy up to wk 60 in patients with rheumatoid…
  • Abstract Number: 2139 • ACR Convergence 2022

    Sustained Response to Guselkumab Regardless of Baseline Demographic, Disease, and Medication Characteristics in Patients with Active Psoriatic Arthritis and an Inadequate Response to TNF Inhibitors: Results from a Phase 3b Trial

    Iain B McInnes1, Philipp Sewerin2, Mohamed Sharaf3, Michela Efficace4, May Shawi5, Michelle Perate6, Miriam Zimmermann7 and Laura Coates8, 1Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom, 2Rheumazentrum Ruhrgebiet, Ruhr-Universität-Bochum, Herne, Germany, 3Johnson & Johnson, Middle East FZ LLC, Dubai, United Arab Emirates, 4Janssen Cilag SpA, Imperia, Italy, 5Immunology Global Medical Affairs, Janssen Pharmaceutical Companies of Johnson & Johnson, Horsham, PA, 6Janssen Scientific Affairs, LLC, Horsham, PA, 7Janssen Scientific Affairs, LLC, Zug, Switzerland, 8Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK, Oxford, England, United Kingdom

    Background/Purpose: Guselkumab (GUS) is a human monoclonal antibody targeting the IL-23 p19 subunit. In the Phase 3b COSMOS trial (NCT03796858), GUS significantly improved disease signs/symptoms…
  • Abstract Number: 0348 • ACR Convergence 2022

    Significant Improvement in Cutaneous Lupus Erythematosus with or Without Systemic Lupus Erythematosus with Belimumab Use – a Systematic Review and Meta-Analysis

    Rachel Kneeland1, Daniel Montes1, Justin endo1, Bridget Shields1, Christie Bartels2 and Shivani Garg3, 1University of Wisconsin, School of Medicine and Public Health, Madison, WI, 2University of Wisconsin School of Medicine and Public Health, Madison, WI, 3University of Madison, School of Medicine and Public Health, Madison, WI

    Background/Purpose: Cutaneous lupus erythematosus (CLE) with or without systemic lupus erythematosus (SLE), can be debilitating and cause significant scarring and psychological distress. Belimumab, a monoclonal…
  • Abstract Number: 0417 • ACR Convergence 2022

    Treating Spondyloarthritis Early: Does It Matter? Results from a Systematic Literature Review

    Dafne Capelusnik1, Diego Benavent2, Désirée van der Heijde3, Robert Landewé4, Denis Poddubnyy5, Astrid van Tubergen6, Louise Falzon7, Victoria Navarro-Compán8 and Sofia Ramiro9, 1Instituto de Rehabilitación Psicofísica (IREP), Buenos Aires, Argentina, 2La Paz University Hospital, Madrid, Spain, 3Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands, Leiden, Netherlands, 4Amsterdam University Medical Centers, Amsterdam, Netherlands, 5Department of Gastroenterology, Infectious Diseases and Rheumatology, Charité – Universitätsmedizin Berlin, Berlin, Germany, 6Maastricht UMC+, Maastricht, Netherlands, 7Health Economics and Decision Science, School of Health and Related Research, University of Sheffield, Sheffield, United Kingdom, 8Department of Rheumatology, La Paz University Hospital, IdiPaz, Madrid, Spain, 9Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: The ASAS-SPEAR (SPondyloarthritis EARly definition) project aims to develop a consensual definition of early SpA. Therefore, it is important to know whether treatment earlier…
  • Abstract Number: 0837 • ACR Convergence 2021

    Sustainability of Response Between Upadacitinib and Adalimumab in Patients with Rheumatoid Arthritis: Results Through 3 Years from the SELECT-COMPARE Trial

    Peter Nash1, Arthur Kavanaugh2, Maya Buch3, Bernard Combe4, Louis Bessette5, In-Ho Song6, Tim Shaw7, Yanna Song6, Jessica Suboticki6 and Roy Fleischmann8, 1Griffith University, Brisbane, Australia, 2University of California San Diego, La Jolla, CA, 3University of Leeds, Leeds, United Kingdom, 4CHU Montpellier Montpellier University, Montpellier, France, 5Laval University, Québec City, QC, Canada, 6AbbVie Inc., North Chicago, IL, 7AbbVie Inc., North Chicago, 8Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX

    Background/Purpose: The primary treatment target for patients with active rheumatoid arthritis (RA) is sustained clinical remission (REM) or low disease activity (LDA).1,2 A greater proportion…
  • Abstract Number: 0953 • ACR Convergence 2021

    An International Delphi Exercise to Identify Items of Importance for Measuring Response to Treatment for ANCA-associated Vasculitis

    Kaitlin Quinn1, Sara Monti2, Georgia Lanier3, Maria Bjork Viðarsdóttir4, Robin Christensen5, David R.W. Jayne6, Carol Langford7, Alfred Mahr8, Christian Pagnoux9, Gunnar Tomasson10 and Peter Merkel11, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), Washington, DC, 2University of Pavia, Pavia, Italy, 3n/a, Sherborn, MA, 4n/a, Reykjavik, Iceland, 5Section for Biostatistics and Evidence-Based Research, the Parker Institute, Bispebjerg and Frederiksberg Hospital, Copenhagen & Research Unit of Rheumatology, Department of Clinical Research, University of Southern Denmark, Copenhagen, Denmark, 6University of Cambridge, Cambridge, United Kingdom, 7Cleveland Clinic, Moreland Hills, OH, 8Kantonsspital St. Gallen, St.Gallen, Switzerland, 9Mount Sinai Hospital, Toronto, ON, Canada, 10University of Iceland, Reykjavik, Iceland, 11University of Pennsylvania, Philadelphia, PA

    Background/Purpose: ANCA-associated vasculitis (AAV) is characterized by fluctuating levels of disease activity. Randomized controlled trials (RCTs) in AAV have used multiple instruments to define active…
  • Abstract Number: 1243 • ACR Convergence 2021

    Real World Validation of a Rule to Predict Response to Sarilumab in Patients with Rheumatoid Arthritis: Analysis from the RISE Registry

    Huifeng Yun1, Jeffrey Curtis2, Lang Chen3, cassie Clinton3, Hubert van Hoogstraten4, Stefano Fiore4, Markus Rehberg5 and Ernest Choy6, 1University of Alabama Birmingham, Birmingham, AL, 2Division of Clinical Immunology and Rheumatology, Department of Medicine, Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 3University of Alabama at Birmingham, Birmingham, AL, 4Sanofi, Bridgewater, NJ, 5Sanofi, Franfurt, Germany, 6CREATE Centre, Cardiff University, Cardiff, Wales, United Kingdom

    Background/Purpose: Accurately identifying patients who may respond better to a specific drug or mechanism of action could improve rational selection of medications to optimize clinical…
  • Abstract Number: 1259 • ACR Convergence 2021

    Association of SLE Responder Index (SRI) Attainment and Long-term Clinical Outcomes

    Kathryn Connelly1, Rangi Kandane-Rathnayake1, Alberta Hoi2, Worawit Louthrenoo3, Laniyati Hamijoyo4, Jiacai Cho5, Aisha Lateef6, Shue-Fen Luo7, Yeong-Jian Wu8, C.S. Lau9, YI-HSING CHEN10, Sandra Navarra11, Leonid Zamora11, Zhanguo Li12, Yuan An12, Sargunan Sockalingam13, Yanjie Hao14, Zhuoli Zhang14, Madelynn Chan15, Yasuhiro Katsumata16, Masayoshi Harigai16, Shereen Oon17, Sang-Cheol Bae18, Sean O’Neill19, Kathryn Gibson19, Jun Kikuchi20, B.M.D.B. Basnayake21, Tsutomu Takeuchi22, Kristine (Pek Ling) Ng23, Fiona Goldblatt24, Annie Law25, Nicola Tugnet26, Yoshiya Tanaka27, Sunil Kumar28, Michael Tee29, Jin Yu Tan30, Chetan Karyekar31, Mandana Nikpour32, Vera Golder1 and Eric Morand33, 1Monash University, Clayton, Australia, 2Department of Rheumatology, Monash Health & Department of Medicine, School of Clinical Sciences, Monash University, Melbourne, Australia, 3Maharaj Nakorn Chiangmai, Chiang Mai, Thailand, 4University of Padjadjaran, Bandung, Indonesia, 5National University Health System (NUHS), Singapore, Singapore, 6National University Hospital, Singapore, Singapore, 7Chang Gung Memorial Hospital, Taipei, Taiwan, 8Chang Gung Memorial Hospital, Taoyuan County, Taiwan, 9University of Hong Kong, Hong Kong, Hong Kong, 10Taichung Veterans General Hospital, Taichung, Taiwan (Republic of China), 11University of Santo Tomas Hospital, Manila, Philippines, 12People's Hospital, Peking University Health Science Center, Beijing, China (People's Republic), 13University of Malaya, Kuala Lumpur, Malaysia, 14Peking University First Hospital, Beijing, China (People's Republic), 15Tan Tock Seng Hospital, Singapore, Singapore, 16Tokyo Women's Medical University School of Medicine, Tokyo, Japan, 17Melbourne Health, Parkville, Australia, 18Hanyang University Medical Center, Seoul, Republic of Korea, 19Liverpool Hospital, Sydney, Australia, 20Keio University School of Medicine, Tokyo, Japan, 21Teaching (General) Hospital, Kandy, Sri Lanka, 22Div. Rheumatology, Keio University, Tokyo, Japan, 23North Shore Hospital, Auckland, New Zealand, 24Flinders Medical Centre, Adelaide, Australia, 25Singhealth, Singapore, Singapore, 26Auckland District Health Board, Auckland, New Zealand, 27University of Occupational and Environmental Health, Kitakyushu, Japan, 28Counties Manukau Health, Auckland, New Zealand, 29University of the Philippines, Quezon City, Philippines, 30Janssen Asia Pacific, Singapore, Singapore, 31Janssen R&D, Spring House, PA, 32University of Melbourne at St Vincent's Hospital, Melbourne, Australia, 33School of Clinical Sciences at Monash Health, Monash University Faculty of Medicine, Nursing and Health Sciences, Monash Medical Centre Clayton, Melbourne, Australia

    Background/Purpose: The SLE Responder Index (SRI) is a composite responder definition employed as a clinical trial endpoint in SLE. Despite its widespread adoption, recent discrepant…
  • Abstract Number: 1694 • ACR Convergence 2021

    Sustainability of Response to Upadacitinib Among Patients with Active Rheumatoid Arthritis Refractory to Biological Disease-Modifying Anti-Rheumatic Drugs

    Ronald van Vollenhoven1, Stephen Hall2, Alvin Wells3, Sebastian Meerwein4, Yanna Song5, Jessica Suboticki5 and Roy Fleischmann6, 1Department of Rheumatology and Clinical Immunology, Amsterdam University Medical Center, Amsterdam Rheumatology Center, Amsterdam, Netherlands, 2Emeritus Research and Monash University, Melbourne, Australia, Melbourne, Australia, 3Rheumatology and Immunotherapy Center, Franklin, WI, 4AbbVie Deutschland GmbH & Co. KG, Ludwigshafen, Germany, 5AbbVie Inc., North Chicago, IL, 6Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX

    Background/Purpose: Sustained clinical remission (REM) is the primary treatment goal for patients with rheumatoid arthritis (RA), with low disease activity (LDA) being an appropriate target…
  • Abstract Number: 1490 • ACR Convergence 2020

    Pain Rating Variability and Response to Treatment in Osteoarthritis Clinical Trials

    Camila Pinto1, Joana Barroso2 and Thomas Schnitzer3, 1Department of Physiology, Northwestern University Feinberg School of Medicine, Chicago, IL, 2Department of Physiology, Northwestern University, Feinberg School of Medicine, Chicago, IL, 3Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Despite the known high inter- and intra-patient variability in analgesic responses in chronic pain, most interventional pain studies rely on single time point pain…
  • Abstract Number: 1515 • ACR Convergence 2020

    Renal Responder Status and Associated Clinical Variables in the Lupus Accelerating Medicines Partnership Cohort

    Philip Carlucci1, Andrea Fava2, Kristina Deonaraine1, Jessica Li3, David Wofsy4, Judith James5, Chaim Putterman6, Betty Diamond7, Derek Fine8, Jose Monroy-Trujillo8, Kristin Haag8, William Apruzzese9, H. Michael Belmont10, Peter Izmirly11, Sean Connery12, Fernanda Payan-Schober12, Richard Furie13, Celine Berthier14, Maria Dall'Era15, Kerry Cho16, Diane Kamen17, Kenneth Kalunian18, The Accelerating Medicines Partnership in SLE Network19, Michelle Petri20 and Jill Buyon21, 1New York University School of Medicine, New York, 2Johns Hopkins, Baltimore, 3Johns Hopkins University, Baltimore, MD, 4University of California San Francisco, San Francisco, CA, 5Oklahoma Medical Research Foundation, Oklahoma City, 6Albert Einstein College of Medicine, Bronx, NY, 7Northwell Health, Hartford, 8Johns Hopkins University, Baltimore, 9., Boston, 10NYU School of Medicine, New York, NY, 11Department of Medicine, New York University School of Medicine, New York, NY, 12Texas Tech University Health Sciences Center, Lubbock, 13Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 14University of Michigan, Ann Arbor, 15Division of Rheumatology, University of California, San Francisco, CA, 16University of California San Francisco, San Francisco, 17Medical University of South Carolina, Charleston, SC, 18School of Health Sciences, University of California, La Jolla, 19Multiple Institutions, Multiple Cities, 20Johns Hopkins University School of Medicine, Baltimore, 21Department of Medicine, NYU School of Medicine, New York, NY

    Background/Purpose: Poor therapeutic response rates contribute to the increased morbidity and mortality associated with lupus nephritis. Early identification of patients likely to respond is crucial…
  • Abstract Number: 1516 • ACR Convergence 2020

    The Value of Renal Biopsy at Lower Levels of Proteinuria in Patients Enrolled in the Lupus Accelerating Medicines Partnership

    Philip Carlucci1, Kristina Deonaraine1, Andrea Fava2, Jessica Li3, David Wofsy4, Judith James5, Chaim Putterman6, Betty Diamond7, Derek Fine8, Jose Monroy-Trujillo8, Kristin Haag8, William Apruzzese9, H. Michael Belmont10, Peter Izmirly11, Sean Connery12, Fernanda Payan-Schober12, Richard Furie13, Celine Berthier14, Maria Dall'Era15, Kerry Cho16, Diane Kamen17, Kenneth Kalunian18, The Accelerating Medicines Partnership in SLE Network19, Michelle Petri20 and Jill Buyon21, 1New York University School of Medicine, New York, 2Johns Hopkins, Baltimore, 3Johns Hopkins University, Baltimore, MD, 4University of California San Francisco, San Francisco, CA, 5Oklahoma Medical Research Foundation, Oklahoma City, 6Albert Einstein College of Medicine, Bronx, NY, 7Northwell Health, Hartford, 8Johns Hopkins University, Baltimore, 9., Boston, 10NYU School of Medicine, New York, NY, 11Department of Medicine, New York University School of Medicine, New York, NY, 12Texas Tech University Health Sciences Center, Lubbock, 13Zucker School of Medicine at Hofstra/Northwell, Great Neck, NY, 14University of Michigan, Ann Arbor, 15Division of Rheumatology, University of California, San Francisco, CA, 16University of California San Francisco, San Francisco, 17Medical University of South Carolina, Charleston, SC, 18School of Health Sciences, University of California, La Jolla, 19Multiple Institutions, Multiple Cities, 20Johns Hopkins University School of Medicine, Baltimore, 21Department of Medicine, NYU School of Medicine, New York, NY

    Background/Purpose: Lupus nephritis continues to be the complication with the highest standardized mortality ratio in Systemic Lupus Erythematosus (SLE), and a late diagnosis associates with…
  • Abstract Number: 1645 • ACR Convergence 2020

    Placebo Group Responses in Clinical Trials of Patients with Osteoarthritis: Data from the Tanezumab Development Program

    Luana Colloca1, Robert Dworkin2, John Farrar3, Leslie Tive4, Ed Whalen5, Jerry Yang4, Lars Viktrup6, Mark Brown7, Christine West7 and Kenneth Verburg8, 1University of Maryland, Baltimore, 2University of Rochester School of Medicine and Dentistry, Rochester, NY, 3University of Pennsylvania, Philadelphia, PA, 4Pfizer Inc, New York, NY, 5Pfizer Inc, New York, 6Eli Lilly and Company, Indianapolis, IN, 7Pfizer Inc, Groton, CT, 8Pfizer Inc, Groton

    Background/Purpose: The level of placebo group response in clinical trials for chronic pain conditions is a concern for the development of novel analgesics1. Here, we…
  • Abstract Number: 1893 • ACR Convergence 2020

    Predictors of Response in Secukinumab-treated Patients with Ankylosing Spondylitis: Logistic Regression and Machine Learning Analyses

    Corinne Miceli-Richard1, Denis Poddubnyy2, Atul Deodhar3, Weibin Bao4, Craig Parman5, Brian Porter6 and Effie Pournara5, 1Paris Descartes University, Department of Rheumatology - Hôpital Cochin, Assistance Publique - Hôpitaux de Paris, Paris, France, 2Charité – Universitätsmedizin Berlin, Berlin, Germany, 3Oregon Health & Science University, Portland, OR, 4Novartis Pharmaceuticals Corporation, East Hannover, 5Novartis Pharma AG, Basel, Switzerland, 6Novartis Pharmaceuticals Corporation, East Hanover, NJ

    Background/Purpose: Predicting outcomes early in the disease course in patients (pts) with ankylosing spondylitis (AS) is challenging, owing to heterogeneity of symptoms, varying disease severity,…
  • « Previous Page
  • 1
  • …
  • 3
  • 4
  • 5
  • 6
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology