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  • Abstract Number: 2628 • 2016 ACR/ARHP Annual Meeting

    Retention of Use and Safety of Subcutaneous Abatacept in Rheumatoid Arthritis: A Patient Record Assessment in a Compassionate Use Programme in South Africa, a Tuberculosis Endemic Country

    I Louw1, M Ally2, DC Janse van Rensburg2, E Van Duuren3, D Nel3, H Miller-Janson4, M de Necker4, JC de Beer4 and H Duvenhage5, 1Panorama Medical Centre, Cape Town, South Africa, 2University of Pretoria, Pretoria, South Africa, 3Jacaranda Hospital, Pretoria, South Africa, 4HEXOR (PTY) Ltd, Pretoria, South Africa, 5Bristol-Myers Squibb, Johannesburg, South Africa

    Background/Purpose: South Africa is a tuberculosis (TB) endemic country having one of the highest TB infection rates in the world with close to 1000 cases…
  • Abstract Number: 2629 • 2016 ACR/ARHP Annual Meeting

    Serious Adverse Events in Patients with RA Taking Abatacept Compared with Other Dmards. Results from a US-Wide Safety Registry

    Kaleb Michaud1,2, Sofia Pedro2, TA Simon3, Frederick Wolfe2 and Rebecca Schumacher2, 1University of Nebraska Medical Center, Omaha, NE, 2National Data Bank for Rheumatic Diseases, Wichita, KS, 3Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: Observational studies are critical in assessing medication safety and effectiveness in the real world. Nonrandom assignment can provide insight to how and when medications…
  • Abstract Number: 2630 • 2016 ACR/ARHP Annual Meeting

    EBV Load Quantification in Peripheral Blood Mononuclear Cells of Patients with Rheumatoid Arthritis Treated By Abatacept and Tocilizumab

    Emmanuel Massy1, Gaétan Texier2, Olivier Muis Pistor3, marielle Martin4, Isabelle Auger5, jean-Pierre Mattei6, Sandrine Guis7, Thao Pham8,9,10, Jean Roudier11,12,13 and Nathalie Balandraud14, 1Rheumatology, Hôpital Sainte Marguerite, marseille, France, 2Centre d'épidémiologie et de santé publique des armées (CESPA) Marseille, marseille, France, 3rheumatology, Hôpital Sainte marguerite, marseille, France, 4INSERM UMRS 1097, marseille, France, 5Université Aix Marseille II, INSERM UMR1097, Marseille, France, 6Rheumatology, Hôpital Sainte Marguerite AP-HM, marseille, France, 7Rheumatology 1, CRMBM-CEMEREM 7339, Aix-Marseille Université, AP-HM, CNRS, Marseilles, France, 8Rheumatology, Service de rhumatoiogie, Marseille, France, 9Rheumatology Department, Sainte Marguerite Hospital, Marseille, France, 10Rheumatology, APHM, Aix Marseille University, Marseille, France, 11Laboratoire d'Immunogénétique de la polyarthrite rhumatoide, INSERM UMR639, Marseille Cedex 09, France, 12Rheumatology 1, Aix Marseille Univ, AP-HM, INSERM, Marseille, France, 13Hopital Sainte Marguerite, Marseille, France, 14Rheumatology 1, AP-HM, INSERM, Marseilles, France

    Background/Purpose: For twenty years, the Epstein-Barr Virus (EBV) has been suspected to contribute to Rheumatoid Arthritis (RA). Immunity against EBV is impaired in RA. RA…
  • Abstract Number: 2631 • 2016 ACR/ARHP Annual Meeting

    Trends and Factors Associated with Use of Biologic Agents As Monotherapy Among US Patients with Rheumatoid Arthritis

    Chieh-I Chen1, Wenhui Wei2, Stuart Blackburn3, Emma Sullivan3 and James Piercy3, 1Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 2Sanofi US, Inc., Bridgewater, NJ, 3Adelphi Real World, Manchester, United Kingdom

    Background/Purpose: For patients with rheumatoid arthritis (RA) receiving a biologic disease-modifying antirheumatic drug (bDMARD), the current standard of care is to use the bDMARD concurrently…
  • Abstract Number: 2632 • 2016 ACR/ARHP Annual Meeting

    Effects of Baseline Patient Characteristics on Baricitinib Efficacy in Patients with Rheumatoid Arthritis

    Joel M. Kremer1, Mark C. Genovese2, David Muram3, Jinglin Zhong4, Jahangir Alam3 and Michael Schiff5, 1Albany Medical College, Albany, NY, 2Stanford University Medical Center, Palo Alto, CA, 3Eli Lilly and Company, Indianapolis, IN, 4Quintiles, Rockville, MD, 5Rheumatology, University of Colorado, Denver, CO

    Background/Purpose : This analysis assessed the effects of baseline patient characteristics on the response to baricitinib treatment in patients with rheumatoid arthritis (RA) and incomplete…
  • Abstract Number: 2633 • 2016 ACR/ARHP Annual Meeting

    Effect of Different Biologic Agents on Lipid Profile in Rheumatoid Arthritis

    Fabio Cacciapaglia1, Simone Perniola1, Mariangela Nivuori1, Margherita Giannini1, Olga Magazzino1, Maria Giannotta1, Florenzo Iannone2 and Giovanni Lapadula1, 1Interdisciplinary Department of Medicine, Rheumatology Unit, University of Bari, General Hospital, Bari, Italy, 2Interdisciplinary Department of Medicine (DIM), Rheumatology Unit, University of Bari, General Hospital, Bari, Italy

    Background/Purpose:  o examine any change between different biologic agents on lipid profile of RA patients. Methods:  Patients affected by RA, according to the 2010 EULAR/ACR…
  • Abstract Number: 2634 • 2016 ACR/ARHP Annual Meeting

    Lack of Autoantibodies to Peptidyl Arginine Deiminase 4 Predict Increased Efficacy of Mavrilimumab in Rheumatoid Arthritis

    Ethan Grant1, Martin Schwickart2, Alex Godwood3, Rachel Moate3, Esther Song2, Carlos Chavez2, Marius Albulescu4, David Close4, Meina Liang2, Tomas Mustelin5, Zhengbin Yao6 and Koustubh Ranade1, 1Translational Medicine, MedImmune, Gaithersburg, MD, 2Clinical Pharmacology and DMPK, MedImmune, Gaithersburg, MD, 3MedImmune, Cambridge, United Kingdom, 4Clinical Development, MedImmune, Cambridge, United Kingdom, 5Respiratory, Inflammation and Autoimmunity, MedImmune, Gaithersburg, MD, 6Respiratory, Inflammation and Autoimmunity iMED, MedImmune, Gaithersburg, MD

    Background/Purpose:  Mavrilimumab is an anti-GM-CSF receptor Ab that has recently demonstrated clinical efficacy in Phase 2 studies in rheumatoid arthritis (RA) patients. Predictive biomarkers to…
  • Abstract Number: 2635 • 2016 ACR/ARHP Annual Meeting

    Using Patient Reported Outcomes to Inform a Treat to Target Treatment Approach in RA

    Eric M. Ruderman1, Jennifer Beaumont2, Emily Bacalao1, George J. Greene2, Azra Muftic2 and David Cella2, 1Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 2Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: The Patient Reported Outcomes Measurement Information System (PROMIS) is an NIH initiative to develop patient-reported outcome measures (PROs) for use across chronic conditions. PROMIS…
  • Abstract Number: 2636 • 2016 ACR/ARHP Annual Meeting

    No Strong Evidence Supporting Predictors for Successful Dose Reduction or Discontinuation of a Biologic in Rheumatoid Arthritis: A Systematic Review

    L. Tweehuysen1, C.H. van den Ende2, F.M.M. Beeren2, E.M.J. Been2, F.H.J. van den Hoogen3,4 and A.A. den Broeder3, 1Sint Maartenskliniek, Nijmegen, Netherlands, 2Rheumatology, Sint Maartenskliniek, Nijmegen, Netherlands, 3Department of Rheumatology, Sint Maartenskliniek, Nijmegen, Netherlands, 4Rheumatology, Radboudumc, Nijmegen, Netherlands

    Background/Purpose: Tapering of biologics in rheumatoid arthritis (RA) is based on a trial-and-error disease activity guided strategy, because it is not known in advance which…
  • Abstract Number: 2637 • 2016 ACR/ARHP Annual Meeting

    Clinical Trials Aiming to Prevent the Development of Rheumatoid Arthritis Cannot Detect Prevention without Adequate Risk Stratification; A Trial Performed in UA-Patients As Example

    Leonie E Burgers, Cornelia F Allaart, Tom WJ Huizinga and Annette HM van der Helm-van Mil, Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose:  Prevention of rheumatoid arthritis (RA) was the aim of several clinical trials performed in undifferentiated arthritis (UA). Overall these trials had negative results. As…
  • Abstract Number: 2638 • 2016 ACR/ARHP Annual Meeting

    In Vitro Expansion of Treg By Adaimumab Predicts Clinical Response to Therapy in Patients with Rheumatoid Arthritis

    Dao Xuan Nguyen, Centre of Rheumatology, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: Regulatory T cells (Treg) are potent suppressors of immune responses and are considered a pivotal element in resolving inflammation and autoimmunity. We have previously…
  • Abstract Number: 2639 • 2016 ACR/ARHP Annual Meeting

    Predicting Flare and Sustained Clinical Remission after Adalimumab Withdrawal Using the Multi-Biomarker Disease Activity (MBDA) Score

    Shintaro Hirata1, Xingbin Wang2, CC Hwang3, Ippei Miyagawa4, Satoshi Kubo1, Kazuhisa Nakano5, Shingo Nakayamada5, Kazuyoshi Saito4, Nadine A. Defranoux2 and Yoshiya Tanaka6, 1The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2Crescendo Bioscience Inc., South San Francisco, CA, 3Biostatistics, Crescendo Bioscience Inc., South San Francisco, CA, 4University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 5First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 6University of Occupational and Environmental Health, Kitakyushu, Japan

    Background/Purpose: The multi-biomarker disease activity (MBDA) (Vectra® DA) score has been reported to predict disease relapses in patients with rheumatoid arthritis (RA) in sustained remission…
  • Abstract Number: 2640 • 2016 ACR/ARHP Annual Meeting

    Can GP88 (Progranulin) be Used to Predict the Efficacy of Infliximab?

    Masao Sato1, Masao Takemura2, Yasuko Yamamoto3 and Kuniaki Saito4, 1Rheumatology, Matsunami General Hospital, Gifu, Japan, 2Advanced Diagnostic System Research Laboratory, Fujita Health University, Toyoake, Japan, 3Disease Control and Prevention, Fujita Health University, Toyoake, Japan, 4Disease Control and Prevention, Fjita Health University, Aichi, Japan

    Background/Purpose:   GP88 (progranulin; PGRN) is a glycoprotein with a molecular weight of approximately 88,000 Da and is thought to play an important role in…
  • Abstract Number: 2641 • 2016 ACR/ARHP Annual Meeting

    Safety of Synthetic and Biological Dmards: Slr Informing the Update of the EULAR Recommendations for the Management of RA

    Sofia Ramiro1, Alexandre Sepriano1, Katerina Chatzidionysiou2, Jackie L. Nam3, Josef Smolen4, Désirée van der Heijde5, Maxime Dougados6, Ronald van Vollenhoven7, Johannes WJ Bijlsma8, GR Burmester9, Marieke Scholte-Voshaar10 and RBM Landewé11, 1Leiden University Medical Center, Leiden, Netherlands, 2Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden, 3Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 4Internal Medicine III, Div. of Rheumatology, Medical University of Vienna, Vienna, Austria, 5Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 6Paris Descartes University, Paris, France, 7Amsterdam Rheumatology Center, Amsterdam, Netherlands, 8Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 9Charité – University Medicine Berlin, Berlin, Germany, 10EULAR Standing Committee of People with Arthritis/Rheumatism in Europe, Zurich, Switzerland, 11Amsterdam Medical Center, Amsterdam, Netherlands

    Background/Purpose: As part of the update of the EULAR recommendations for the management of RA, we performed a systematic literature review to assess the safety…
  • Abstract Number: 2643 • 2016 ACR/ARHP Annual Meeting

    Risk Factors of Pneumocystis Jiroveci Pneumonia (PJP) in Patients with RA and Sulfasalazine As a Possible Protective Agent

    Shinji Motojima1, Tamao Nakashita2, Akira Jibatake1, Akira Yoshida1 and Yoshiki Yamamoto1, 1Department of Rheumatology and Allergy, Kameda Medical Center, Kamogawa city, Japan, 2Department of Rheumatology and Allergy, Kameda Medical Center, Kamogawa-city, Japan

    Background/Purpose:  Pneumocystis jiroveci pneumonia (PJP) is a serious complication during the treatment in patients with variety of rheumatic disease. Postmarketing surveillance of infliximab and etnercept…
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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 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.).

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