ACR Meeting Abstracts

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Abstracts tagged "DMARDs"

  • Abstract Number: 557 • 2015 ACR/ARHP Annual Meeting

    Early Intensification of Treatment Induces Superior Outcomes in Two Randomized Trials According to Predicted Vs. Observed Radiographic Progression in Rheumatoid Arthritis

    Adrian Levitsky1, Marius C. Wick2, Timo Möttönen3, Marjatta Leirisalo-Repo4, Leena Laasonen5, Hannu Kautiainen6,7, Markku Korpela8, Ronald F. van Vollenhoven1 and Vappu Rantalaiho8, 1Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden, 2Radiology, Karolinska University Hospital, Stockholm, Sweden, 3Internal Medicine, Division of Rheumatology, Turku University Central Hospital, Turku, Finland, 4Rheumatology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland, 5Helsinki Medical Imaging Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland, 6Unit of Primary Health Care, University of Helsinki and Helsinki University Hospital, Helsinki, Finland, 7Unit of Primary Health Care, Kuopio University Hospital, Kuopio, Finland, 8Department of Internal Medicine, Center for Rheumatic Diseases, Tampere University Hospital, Tampere, Finland

    Background/Purpose: Predicted vs. Observed Radiographic Progression in early Rheumatoid Arthritis (POPeRA) is a method that has previously confirmed the relative radiographic efficacy of synthetic disease-modifying…
  • Abstract Number: 1639 • 2015 ACR/ARHP Annual Meeting

    Clinical Outcomes for Rheumatoid Arthritis Patients Receiving Tofacitinib Monotherapy in the Open-Label Long-Term Extension over 6 Years

    Roy Fleischmann1, Yusuf Yazici2, Jürgen Wollenhaupt3, Lisy Wang4, Anna Maniccia5, Kenneth Kwok4, Liza Takiya5 and Ronald van Vollenhoven6, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2New York University Hospital for Joint Diseases, New York, NY, 3Teaching Hospital of the University of Hamburg, Schoen-Klinik Hamburg-Eilbek, Hamburg, Germany, 4Pfizer Inc, Groton, CT, 5Pfizer Inc, New York, NY, 6The Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Treatment options delivering sustained efficacy when given as monotherapy in RA are limited.1 Tofacitinib is an oral Janus kinase inhibitor for the treatment of…
  • Abstract Number: 2768 • 2015 ACR/ARHP Annual Meeting

    Trend and Factors Associated with Switching Treatment after Initial Anti-TNF Therapy Among Patients with Rheumatoid Arthritis

    Wenhui Wei1, Emma Sullivan2, Chieh-I Chen3, James Piercy2 and Stuart Blackburn2, 1Sanofi-Aventis, Bridgewater, NJ, 2Adelphi Real World, Manchester, United Kingdom, 3Regeneron Pharmaceuticals, Inc., Tarrytown, NY

    Background/Purpose: Among rheumatoid arthritis (RA) patients who progress beyond their first biologic disease-modifying antirheumatic drug (bDMARD), in-class cycling between different tumor necrosis factor inhibitors (TNFi)…
  • Abstract Number: 602 • 2015 ACR/ARHP Annual Meeting

    Efficacy of Very Low Dose (100mg) Rituximab in Active Rheumatoid Arthritis Despite Combination DMARD-Single Center, Prospective, Observational Study

    Padmanabha Shenoy1 and Manish Bavaliya2, 1Dept. of rheumatology and clinical immunology, Amrita Institute of medical science and research institute, Kochi, India, 2Department of rheumatology and clinical immunology, Amrita institute of medical sciences and research institute, Kochi, India

    Background/Purpose: Rituximab is an anti-CD20 antibody that represents a therapeutic alternative for the patients with rheumatoid arthritis. It has been proven that rituximab at a…
  • Abstract Number: 1640 • 2015 ACR/ARHP Annual Meeting

    Effect of Methotrexate Dose on the Efficacy of Tofacitinib: Treatment Outcomes from a Phase 3 Clinical Trial of Patients with Rheumatoid Arthritis

    Roy Fleischmann1, Philip J. Mease2, Sergio Schwartzman3, Lie-Ju Hwang4, Aditya Patel5, Koshika Soma4, Carol A. Connell6, Liza Takiya4 and Eustratios Bananis7, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2Rheumatology Research, Swedish Medical Center, Seattle, WA, 3Hospital for Special Surgery, New York, NY, 4Pfizer Inc, New York, NY, 5Inventiv Health Inc, South Plainfield, NJ, 6Pfizer Inc, Groton, CT, 7Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). ORAL Scan was a 2-year, randomized, Phase 3, clinical trial…
  • Abstract Number: 2769 • 2015 ACR/ARHP Annual Meeting

    Factors Associated with TNF Switching: a Retrospective Real-World Study of Patients with Rheumatoid Arthritis

    Wenhui Wei1, Keith Knapp2, Li Wang3, Chieh-I Chen4, Gary Craig2, Karen Ferguson2 and Sergio Schwartzman5, 1Sanofi-Aventis, Bridgewater, NJ, 2Discus Analytics, Inc., Spokane, WA, 3Director, Analytic Research, STATinMED Research, Plano, TX, 4Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 5Hospital for Special Surgery, New York, NY

    Background/Purpose: Switching of disease-modifying antirheumatic drugs (DMARDs) in rheumatoid arthritis (RA) patient treatment is common in real-world clinical practice. The context for why patients switch…
  • Abstract Number: 618 • 2015 ACR/ARHP Annual Meeting

    The Multi-Biomarker Disease Activity Score in Methotrexate Incomplete Responders Predicts Clinical Responses to Non-Biological Versus Biological Therapy in Early RA

    Karen Hambardzumyan1, Rebecca J. Bolce2, Saedis Saevarsdottir3, Kristina Forslind4,5, Johan A Karlsson6 and Ronald F. van Vollenhoven1, 1Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden, 2Crescendo Bioscience Inc., South San Francisco, CA, 3Department of Medicine, Rheumatology Unit, The Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden, 4Department of Medicine, Helsingborgs Lasarett, Section of Rheumatology, Helsingborg, Sweden, 5Departments of Rheumatology, Helsingborgs Hospital and University of Lund, Helsingborg and Lund, Sweden, 6Section of Rheumatology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden

    Background/Purpose: The Swedish Farmacotherapy (SWEFOT) trial and other trials in rheumatoid arthritis (RA) demonstrated that in MTX incomplete responder patients (MTX-IR) the addition of anti-TNF…
  • Abstract Number: 1669 • 2015 ACR/ARHP Annual Meeting

    Serum Survivin Predicts Responses to Treatment in Active Rheumatoid Arthritis

    Adrian Levitsky1, Malin C. Erlandsson2, Ronald F. van Vollenhoven1 and Maria I. Bokarewa2, 1Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden, 2Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden

    Background/Purpose: Survivin is an oncological biomarker. In rheumatoid arthritis (RA), elevated serum survivin is common and has been used to predict disease onset and progressive…
  • Abstract Number: 2783 • 2015 ACR/ARHP Annual Meeting

    What Is the Rate of Primary and Secondary Failure of Anti-TNF in RA Patients? Data from a Rheumatoid Arthritis Cohort

    Edward C. Keystone1, Mohammad Movahedi2,3, Angela Cesta2, Xiuying Li2, Sandra Couto2, Emmanouil Rampakakis3, John S. Sampalis3,4, Claire Bombardier2,5,6 and OBRI Investigators, 1The Rebecca MacDonald Centre For Arthritis, Mount Sinai Hospital, Toronto, ON, Canada, 2Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada, 3JSS Medical Research, St-Laurent, QC, Canada, 4McGill University, Montreal, QC, Canada, 5University of Toronto, Department of Medicine (DOM) and Institute of Health Policy Management, and Evaluation (IHPME), Toronto, ON, Canada, 6Division of Rheumatology, Mount Sinai Hospital, Toronto, ON, Canada

    Background/Purpose: Although the majority of RA patients respond to treatment with anti-TNF agents, some patients present with refractory disease (1ry failure) while others show some…
  • Abstract Number: 705 • 2015 ACR/ARHP Annual Meeting

    Sex Differences in Psoriatic Arthritis: Evaluation of a Real-Life Cohort of 2,118 Italian Patients Treated with Methotrexate

    Carlo Selmi1,2, Elena Generali3, Greta Carrara4, Carlo Alberto Scirè4 and RECORD Study Group of the Italian Society for Rheumatology, 1BIOMETRA Department, University of Milan, Milan, Italy, 2Internal Medicine- Unit of Rheumatology and Clinical Immunology, Humanitas Clinical and Research Center, Rozzano, Italy, 3Internal Medicine- Unit of Rheumatology and Clinical Immunology, Humanitas Clinical and Research Center, Rozzano (MI), Italy, 4Epidemiology Unit – Italian Society for Rheumatology (SIR), Milano, Italy

    Background/Purpose: The influence of sex in psoriatic arthritis (PsA) features and treatment outcomes has not been fully elucidated. We investigated the differences between sexes in…
  • Abstract Number: 1676 • 2015 ACR/ARHP Annual Meeting

    Systematic Review and Network Meta-Analysis of Combination Treatments in Disease Modifying Anti-Rheumatic Drug Experienced Patients with Severe Rheumatoid Arthritis: Analysis of American College of Rheumatology Criteria Scores 20, 50, and 70: An Update

    Michelle E. Orme1, Charles Hawes2 and Stephen A. Mitchell3, 1ICERA consulting UK, Swindon, United Kingdom, 2Pfizer UK, Surrey, United Kingdom, 3Abacus International UK, Bicester, United Kingdom

    Background/Purpose: Biologic disease-modifying anti-rheumatic drugs (DMARDs) in combination with conventional DMARDs provide patients with severe rheumatoid arthritis (RA) and an inadequate response to conventional DMARDs…
  • Abstract Number: 2790 • 2015 ACR/ARHP Annual Meeting

    Leflunomide/Hydroxychoroquine Combination Treatment Additively Inhibits T Cell Receptor/Toll-like Receptor 9-Triggered Th1 and Th17 Cytokine Secretion 

    E.H.M. van der Heijden1,2, S.A.Y. Hartgring1, S. Hiddingh1, A.A. Kruize2, T.R.D.J. Radstake1,3 and J.A.G. van Roon1, 1Laboratory for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 2Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 3Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose:  Primary Sjögren’s Syndrome (pSS) is a systemic auto-immune disease, leading to an exocrinopathy of mainly salivary and lachrymal glands. T- and B-cell-driven immunity is…
  • Abstract Number: 707 • 2015 ACR/ARHP Annual Meeting

    Change of Enthesial Involvement Under Treatment Was Independent from the Therapeutic Strategy in Patients with Axial Spondyloarthritis within the Scqm Cohort

    Ruediger Mueller1, Toni Kaegi2, Nicole Graf3, Johannes von Kempis4 and J.J. Luime5, 1Rheumatology, MD, St. Gallen, Switzerland, 2Kantonsspital St. Gallen, St. Gallen, Switzerland, 3graf biostatistics, Winterthur, Switzerland, 4Rheumatology, Kantonsspital St. Gallen, St. Gallen, Switzerland, 5Department of Rheumatology, Erasmus Medical Centre, Rotterdam, Netherlands

    Background/Purpose: Enthesitis is one of the potential extra-axial manifestations found in patients with spondyloarthritis (SpA). Enthesitis can be quantified using the MASES (Maastrich Ankylosing Spondylitis…
  • Abstract Number: 1932 • 2015 ACR/ARHP Annual Meeting

    IL-17A-Low CCR6+ Th Cell Populations of Patients with Rheumatoid Arthritis Are Pathogenic, Multidrug Resistant and Associated with DMARD and Glucocorticoid Treatment Response

    Jan Piet van Hamburg1, Sandra M.J. Paulissen2, Nadine Davelaar1, Mieke Hazes3 and Erik Lubberts1, 1Rheumatology and Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 2Room Nb-84, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands

    Background/Purpose: CCR6+ T-helper (Th) cells and their pro-inflammatory cytokines including IL-17A are implicated in the pathogenesis of rheumatoid arthritis (RA). However, within the CCR6+ Th…
  • Abstract Number: 2837 • 2015 ACR/ARHP Annual Meeting

    Sulfasalazine Comedication: A Predictor of Reduced Long-Term Anti-TNF Switch in Ankylosing Spondylitis

    Andrea Y. Shimabuco, Celio R. Gonçalves, Julio C. B. Moraes, Mariana G Waisberg, Percival D Sampaio-Barros, Cláudia Goldenstein-Schainberg, Eloisa Bonfá and Carla G.S. Saad, Rheumatology Division, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil

    Background/Purpose: Anti-TNF agents are efficacious in the treatment of ankylosing spondylitis (AS). The switch to another TNF blockage can be an alternative in cases of…
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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 ET on November 14, 2024. 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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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