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Abstracts tagged "rheumatoid arthritis (RA) and treatment"

  • Abstract Number: 447 • 2015 ACR/ARHP Annual Meeting

    Components of Treatment Delay in Rheumatoid Arthritis Differ According to Autoantibody Status

    Arthur G Pratt1, Ben Hargreaves2, Dennis W Lendrem2, Osman Aslam2 and John D Isaacs2, 1Institute of Cellular Medicine (Musculoskeletal Research Group), National Institute for Health Research Newcastle Biomedical Research Centre based at Newcastle Hospitals Foundation Trust and Newcastle University, Newcastle upon Tyne, United Kingdom, 2Institute of Cellular Medicine (Musculoskeletal Research Group), NIHR Newcastle Biomedical Research Centre, Newcastle Hospitals Foundation Trust and Newcastle University, Newcastle upon Tyne, United Kingdom

    Background/Purpose: Despite a proliferation of early arthritis (EA) clinics intended to expedite the diagnosis of rheumatoid arthritis (RA), patients continue to experience substantial and multifactorial…
  • Abstract Number: 2491 • 2015 ACR/ARHP Annual Meeting

    Documentation of Disease Activity Score As Part of a Treat to Target Strategy in Rheumatoid Arthritis

    Sarah Homann1 and Beth Scholz2, 1Rheumatology, University of Texas Health Sciences Center at Houston, Houston, TX, 2University of Texas Health Sciences Center at Houston, Houston, TX

    Background/Purpose: Compared to routine care, the Treat to Target (TTT) strategy for rheumatoid arthritis (RA) has been validated to improve functional and radiographic outcomes via…
  • Abstract Number: 458 • 2015 ACR/ARHP Annual Meeting

    First Year Canadian Experience with Subcutaneous Abatacept in Routine Practice for the Treatment of Patients with Rheumatoid Arthritis: Data from the Orencia Response Program (ORP) Network

    Boulos Haraoui1, Louis Coupal2, Radmila Day3, Lionel Budry4 and Youb Chalabi5, 1Institut de Rhumatologie de Montréal and University of Montreal, Montreal, QC, Canada, 2Rheumatology, Institut de recherche en rhumatologie de Montréal (IRRM), Montréal, QC, Canada, 3None, Montreal, QC, Canada, 4Bristol Myers Squibb Canada, St-Laurent, QC, Canada, 5Bristol Myers Squibb, Montreal, QC, Canada

    Background/Purpose: The subcutaneous (SC) formulation of abatacept (ABA) has been available in Canada since January 2014. Here we report first year experience with SC ABA…
  • Abstract Number: 2656 • 2015 ACR/ARHP Annual Meeting

    Analysis of Morning Stiffness Response in Rheumatoid Arthritis Patients with Low Disease Activity Receiving Delayed-Release Prednisone Plus Dmards As Compared to Placebo Plus Dmards

    Rieke Alten1, Robert J. Holt2, Jeffrey D. Kent3 and Frank Buttgereit4, 1Charité Univ Medicine, Berlin, Germany, 2College of Pharmacy, University of Illinois-Chicago, Vernon Hill, IL, 3Medical Affairs, Horizon Pharma, Inc, Deerfield, IL, 4Charité-Universitätsmedizin Berlin, Free University and Humboldt University of Berlin, Berlin, Germany

    Background/Purpose: Patient reported outcomes such as morning stiffness are reported frequently in rheumatoid arthritis (RA) patients. But little has been reported about the presence and…
  • Abstract Number: 1903 • 2014 ACR/ARHP Annual Meeting

    Change in 14-3-3η Expression in Early RA Patients Treated with Dmards Corresponds with Change in DAS28 and Good EULAR Responses

    Dirkjan van Schaardenburg1, Mairead Murphy2, Yuan Gui2, Samina Turk3, Walter P. Maksymowych4 and Anthony Marotta5, 1Dr Jan van Breemenstraat 2, Reade, Amsterdam, Netherlands, 2Augurex Life Sciences Corp., North Vancouver, BC, Canada, 3Reade, Amsterdam, Netherlands, 4Medicine/Rheumatic Dis Unit, University of Alberta, Edmonton, AB, Canada, 51423 Dempsey Road, Augurex Life Sciences Corp., North Vancouver, BC, Canada

    Background/Purpose 14-3-3η is a mechanistic marker that up-regulates inflammatory and joint damage factors that are implicated in the RA pathophysiological process1. It is a potent…
  • Abstract Number: 1847 • 2014 ACR/ARHP Annual Meeting

    Effect of Disease Duration on Clinical Outcomes in Moderate Rheumatoid Arthritis Patients Treated with Etanercept Plus Methotrexate in the Preserve Study

    Josef Smolen1, David Collier2, Annette Szumski3, Heather Jones4 and Lisa Marshall5, 1PsAID taskforce, EULAR, Zurich, Switzerland, 2Amgen, Inc., Thousand Oaks, CA, 3Specialty Care, Pfizer Inc., Collegeville, PA, 4Inflammation & Immunology, Pfizer Inc., Collegeville, PA, 5Inflammation Immunology Disease Group, Pfizer Inc., Collegeville, PA

    Background/Purpose Previous studies evaluating various treatment strategies indicate that disease duration is a key determinant of outcomes in rheumatoid arthritis (RA). While data suggest that…
  • Abstract Number: 1540 • 2014 ACR/ARHP Annual Meeting

    Treatment Patterns of Biologics Used in Rheumatoid Arthritis and Ankylosing Spondylitis in the US Veterans Population

    Brian Sauer1, Chia-Chen Teng1, Tao He1, Jianwei Leng2, Chao-Chin Lu1, Neel Shah3, David J. Harrison4, Derek Tang4 and Grant W. Cannon5, 1Salt Lake City VA and University of Utah, Salt Lake City, UT, 2Salt Lake City VA and University of Utah, Salt Lake Citty, UT, 31 Amgen Center Dr, Amgen Inc., Thousand Oaks, CA, 4Amgen Inc., Thousand Oaks, CA, 5Division of Rheumatology, Salt Lake City VA and University of Utah, Salt Lake City, UT

    Background/Purpose: Biologics used for rheumatoid arthritis (RA) and ankylosing spondylitis (AS), including tumor necrosis factor blockers, are a key area of focus for Veterans Affairs…
  • Abstract Number: 1514 • 2014 ACR/ARHP Annual Meeting

    An Analysis of in-Vitro Cytokine Inhibition Profiles of Tofacitinib and Other Janus Kinase Inhibitors at Clinically-Meaningful Concentrations

    M.E. Dowty, T.S. Lin, L. Wang, J. Jussif, B. Juba, L. Li, E. Moy and J.-B. Telliez, Pfizer Worldwide R&D, Cambridge, MA

    Background/Purpose: A number of Janus kinase (JAK) inhibitors are being actively investigated for treatment of rheumatoid arthritis (RA), including tofacitinib, baricitinib, filgotinib (GLPG0634), and decernotinib…
  • Abstract Number: 1485 • 2014 ACR/ARHP Annual Meeting

    Analysis of Patient-Reported Outcomes during Treatment with Mavrilimumab, a Human Monoclonal Antibody Targeting GM-CSFRá, in the Randomized Phase 2b Earth Explorer 1 Study

    Joel M. Kremer1, Gerd Burmester2, Michael Weinblatt3, Angela Williams4, Niklas Karlsson5, Alex Godwood6 and David Close7, 1Medicine, Albany Medical College and the Center for Rheumatology, Albany, NY, 2Department of Rheumatology and Clinical Immunology, Charité University Medicine, Berlin, Germany, 3Rheumatology, Brigham & Women's Hospital, Harvard Medical School, Boston, MA, 4MedImmune Ltd, Cambridge, United Kingdom, 5Health Economics and Outcomes Research, AstraZeneca, Molndal, Sweden, 6Clinical Biostatics and Data Management, MedImmune Ltd, Cambridge, United Kingdom, 7Clinical Development, MedImmune Ltd, Cambridge, United Kingdom

    Background/Purpose Active RA significantly impairs health-related quality of life (HRQoL) and physical function of patients. Granulocyte-macrophage colony-stimulating factor (GM-CSF) plays a key role in macrophage…
  • Abstract Number: 1452 • 2014 ACR/ARHP Annual Meeting

    Timing of Decisions to Adjust Disease Modifying Anti-Rheumatic Drug (DMARD) Therapy for Rheumatoid Arthritis (RA) Patients with Active Disease in a Usual Practice Setting

    Yomei Shaw1, Chung-Chou H. Chang2, Marc C. Levesque3, Julie M. Donohue4, Kaleb Michaud5,6 and Mark S. Roberts1, 1Department of Health Policy and Management, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, 2Department of Medicine, University of Pittsburgh Department of Medicine, Pittsburgh, PA, 3Division of Rheumatology and Clinical Immunology, University of Pittsburgh Department of Medicine, Pittsburgh, PA, 4Health Policy & Management, University of Pittsburgh Graduate School of Public Health, Pittsburgh, PA, 5National Data Bank for Rheumatic Diseases, Wichita, KS, 6Internal Medicine, Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: Current guidelines recommend that rheumatoid arthritis (RA) patients with poor response to their current regimen of disease modifying anti-rheumatic drugs (DMARDs) have therapy adjusted…
  • Abstract Number: 2923 • 2014 ACR/ARHP Annual Meeting

    Protein Quantification Using Mass Spectrometry Methods to Predict Response to Abatacept and Methotrexate Combination Therapy in Rheumatoid Arthritis

    A Obry1,2, P Cosette2, T Lequerré1,3, Maria-Antonietta d'Agostino4, C Gaillez5, M Le Bars6 and O Vittecoq1,3, 1Inserm 905, Institute for Biomedical Research, University of Rouen, Rouen, France, 2UMR 6270 CNRS, PISSARO Proteomic Facility, IRIB, Normandy University, University of Rouen, Rouen, France, 3Department of Rheumatology, Rouen University Hospital, Rouen, France, 4AP-HP Ambroise Paré Hospital, Boulogne-Billancourt, France, 5Formerly of Bristol-Myers Squibb, Rueil-Malmaison, France, 6Bristol-Myers Squibb, Rueil-Malmaison, France

    Background/Purpose: Targeted biologic therapies with different mechanisms of action are commonly used in RA. Abatacept is a recombinant fusion protein that inhibits T-cell co-stimulatory molecules…
  • Abstract Number: 1407 • 2014 ACR/ARHP Annual Meeting

    Low HAQ and Pain Predict Patient Perceived Remission in Rheumatoid Arthritis Patients Receiving MTX or Anti-TNF-Alpha Treatment

    Paul Studenic1, Josef Smolen2 and Daniel Aletaha1, 1Department of Internal Medicine 3, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 2Department of Medicine 3, Division of Rheumatology, Medical University of Vienna and Hietzing Hospital, Vienna, Austria

    Background/Purpose The induction of remission is the primary target of RA therapy. Failing to achieve the patient global estimate of disease activity criterion (PGA
  • Abstract Number: 2912 • 2014 ACR/ARHP Annual Meeting

    Impact of Failure to Adhere to Treat-to-Target of Rheumatoid Arthritis in Real World Practice: Data from the International Rheumatoid Arthritis Biomarker Program

    Walter P. Maksymowych1,2, M. Østergaard3, O Elkayam4, R Landewé5, J Homik6, C Thorne7, M Backhaus8, S Shaikh9, G Boire10, M Larche11, B Combe12, T Schaeverbeke13, A Saraux14, G Ferraccioli15, M Dougados16, C Barnabe17, M Govoni18, PP Tak19, D. van Schaardenburg20, D van der Heijde21, R Dadashova2, E Hutchings2, J Paschke2 and Oliver FitzGerald22, 1Medicine, University of Alberta, Edmonton, AB, Canada, 2CaRE Arthritis, Edmonton, AB, Canada, 3Copenhagen Center for Arthritis Research, Glostrup, Denmark, 4Tel Aviv Sourasky Medical Center, Tel Aviv, Israel, 5Amsterdam Rheumatology Center, Amsterdam, Netherlands, 6University of Alberta, Edmonton, AB, Canada, 7Southlake Regional Health Centre, Newmarket, ON, Canada, 8Rheumatology/Immunology, Charite University Hospital, Berlin, Germany, 9Niagara Peninsula Arthritis Centre, Hamilton, ON, Canada, 10CHUS-Sherbrooke University, Sherbrooke, QC, Canada, 11St Joseph's Healthcare Hamilton, Hamilton, ON, Canada, 12Immuno-Rhumatologie, Hôpital Lapeyronie, Montpellier, France, 13Bordeaux University Hospital, Bordeaux, France, 14CHU Brest and EA 2216, UBO, Brest, France, 15Catholic University of The Sacred Heart, Rome, Italy, 16Hopital Cochin, Paris, France, 17University of Calgary, Calgary, AB, Canada, 18Universita di Ferrara, Ferrara, Italy, 19Academic Medical Center, Amsterdam, Netherlands, 20Jan van Breemen Research Institute, Amsterdam, Netherlands, 21Leiden University Medical Center, Leiden, Netherlands, 22St. Vincent's University Hospital, Dublin, Ireland

    Background/Purpose . There is limited data on adherence to treat-to-target (T2T) strategies in RA in real world-practice and the impact of failure to adopt this…
  • Abstract Number: 1384 • 2014 ACR/ARHP Annual Meeting

    Fibromyalgia and Its Effect on Treatment Response in Early Rheumatoid Arthritis Patients  

    Josefina Durán Santa Cruz1, Bernard Combe2, Jingbo Niu1, Nathalie Rincheval3, Cécile Gaujoux-Viala4 and David T. Felson5, 1Clinical Epidemiology Research and Training Unit, Boston University School of Medicine, Boston, MA, 2Immuno-Rhumatologie, Hôpital Lapeyronie, Montpellier, France, 3Institut Universitaire de Recherche Clinique, Montpellier, France, 4EA 2415, Montpellier I University, Nîmes University Hospital, Rheumatology Department, Nîmes, France, 5Clinical Epidemiology Unit, Boston University School of Medicine, Boston, MA

    Background/Purpose: Fibromyalgia (FM) occurs commonly in patients with rheumatoid arthritis (RA) and its effect on treatment response is unknown. In this study we aimed to…
  • Abstract Number: 2517 • 2014 ACR/ARHP Annual Meeting

    Long-Term Clinical, Structural, and Functional Consequences of Not Adopting Treatment in MTX Suboptimal Responders

    Josef Smolen1, Ronald F. van Vollenhoven2, Stefan Florentinus3, Yijie Zhou4, Benoit Guerette4 and Arthur Kavanaugh5, 1Medical University of Vienna and Hietzing Hospital, Vienna, Austria, 2The Karolinska Institute, Stockholm, Sweden, 3AbbVie, Rungis, France, 4AbbVie, Inc., North Chicago, IL, 5University of California San Diego, La Jolla, CA

    Background/Purpose: Methotrexate (MTX) is used as first line therapy for treatment of rheumatoid arthritis (RA). Current recommendations state that therapy should be adjusted if patients…
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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].

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