ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "biologic response modifiers"

  • Abstract Number: 1174 • 2012 ACR/ARHP Annual Meeting

    Severe Adverse Events Associated with Use of Biologic Therapy in Juvenile Idiopathic Arthritis: A Single-Center Study

    Ricardo A. G. Russo1 and Marìa M. Katsicas2, 1Immunology & Rheumatology, Hospital de Pediatria Garrahan, Buenos Aires, Argentina, 2Immunology & Rheumatology., Hospital de Pediatrìa Garrahan, Buenos Aires, Argentina

    Background/Purpose: biologic agents have revolutionized the treatment of Juvenile Idiopathic Arthritis (JIA) and other conditions due to their high efficacy and safety. However, with the…
  • Abstract Number: 2172 • 2012 ACR/ARHP Annual Meeting

    An Update of Management of Coccidioidomycosis in Patients On Biologic Response Modifiers and Disease-Modifying Antirheumatic Drugs

    Susan Knowles1, Dominick Sudano1, Sara Taroumian2, Neil M. Ampel3, John Galgiani4, Jeffrey R. Lisse1 and Susan E. Hoover5, 1Department of Rheumatology, University of Arizona, Tucson, AZ, 2Department of Rheumatology, University of California, Los Angeles, Los Angeles, CA, 3Infectious Disease, University of Arizona, Tucson, AZ, 4Valley Fever Center for Excellence, Tucson, AZ, 5Infectious Diseases, University of Arizona, Tucson, AZ

    Background/Purpose: Coccidioidomycosis (valley fever) is an endemic fungal infection in the Southwestern United States which typically causes a self-limited pulmonary illness. Patients with rheumatic disease…
  • Abstract Number: 1142 • 2012 ACR/ARHP Annual Meeting

    Efficacy of Biologic Agents in Juvenile Idiopathic Arthritis: A Systematic Review Using Indirect Comparisons

    Janneke Anink1, Marieke H. Otten1, Sandra Spronk2 and Lisette W.A. Van Suijlekom-Smit1, 1Pediatric Rheumatology, Erasmus MC Sophia Children's Hospital, Rotterdam, Netherlands, 2Department of Epidemiology and Radiology, Erasmus MC, Rotterdam, Netherlands

    Background/Purpose: During the last decade the availability of biologic agents for the treatment of juvenile idiopathic arthritis (JIA) increased substantially. Because direct head-to-head trials comparing…
  • Abstract Number: 2155 • 2012 ACR/ARHP Annual Meeting

    The Annualized Progression of Radiologic Damage in Placebo Arms of Rheumatoid Arthritis Trials Is Much Lower Than the Mean Annual Progression Since Disease Onset

    Jean-Marie Berthelot and Celine Cozic, Rheumatology Unit, Nantes University Hospital, Nantes, France

    Background/Purpose : A previous meta-analysis by Graudal and Jürgens (Arthritis Rheum. 2010;62:2852–63) challenged the belief that biologics better protect rheumatoid arthritis (RA) from joint destruction…
  • Abstract Number: 1145 • 2012 ACR/ARHP Annual Meeting

    Use of Non-Etanercept Biologics in Children with Juvenile Idiopathic Arthritis: Results From the Biologics for Children with Rheumatic Diseases Study

    Lianne Kearsley-Fleet1, Eileen Baildam2, Michael Beresford3, Rebecca Davies4, Helen E. Foster5, Katy Mowbray1, Taunton R. Southwood6, Wendy Thomson1 and Kimme L. Hyrich7, 1Arthritis Research UK Epidemiology Unit, Manchester Academic Health Science Centre, Manchester, United Kingdom, 2Paediatric Rheumatology, Alder Hey Children's Foundation NHS Trust, Liverpool, United Kingdom, 3University of Liverpool, Institute of Translational Medicine (Child Health), Alder Hey Children's Foundation NHS Trust, Liverpool, United Kingdom, 4Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester, United Kingdom, 5Institute Cellular Medicine, Musculoskeletal Research Group, Newcastle upon Tyne, United Kingdom, 6Institute of Child Health, University of Birmingham and Birmingham Children's Hospital, Birmingham, United Kingdom, 7Centre for Musculoskeletal Research, University of Manchester, Manchester, United Kingdom

    Background/Purpose: The management of juvenile idiopathic arthritis (JIA) has been revolutionised by the introduction of biologic therapy, although the majority remain unlicensed for children. Until…
  • Abstract Number: 2093 • 2012 ACR/ARHP Annual Meeting

    Rates of Opportunistic Infections Among Rheumatoid Arthritis Patients Switching Biologic Therapy

    John Baddley1, Shuo Yang2, Klye Brizendine3, Scott DuVall4, Kevin L. Winthrop5, Mary J. Burton6, Nivedita M. Patkar7, Elizabeth S. Delzell8, Monika M. Safford9, Jasvinder A. Singh10, Iris E. Navarro11, Grant W. Cannon12, Ted R. Mikuls13, Lang Chen11, Kenneth G. Saag14, Kimberly Alexander15, Pavel Napalkov15, Aaron Kamauu16 and Jeffrey R. Curtis17, 1Medicine, University of Alabama at Birmingham, Birmingham, AL, 2Clinical Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Infectious Disease, Birmingham, AL, 4VA Salt Lake City Health Care System and University of Utah School of Medicine, Salt Lake City, UT, 5Dept of Infectious Disease, Oregon Health & Science University, Portland, OR, 6VA Hospital, Jackson, MS, 7Immunology/Rheumatology, Univ of Alabama-Birmingham, Birmingham, AL, 8Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 9Preventive Medicine, University of Alabama at Birmingham, Birmingham, AL, 10Department of Medicine, University of Alabama, Tuscaloosa, AL, 11Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 12Division of Rheumatology, George E. Wahlen VA Medical Center, Salt Lake City, UT, 13Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE, 14Div Clinical Immun & Rheum, Univ of Alabama-Birmingham, Birmingham, AL, 15Epidemiology, Genentech, Inc., South San Francisco, CA, 16Anolinx, Bountiful, UT, 17Rheumatology & Immunology, Univ of Alabama-Birmingham, Birmingham, AL

    Background/Purpose: The incidence of opportunistic infections (OIs) in patients on biologics is low, but may approach several cases per 100 person-years (PY). Data on risks…
  • Abstract Number: 1146 • 2012 ACR/ARHP Annual Meeting

    Choice of Systemic JIA Treatment Among Childhood Arthritis and Rheumatology Research Alliance (CARRA) Rheumatologists

    Jennifer E. Weiss1, Esi M. Morgan DeWitt2, Timothy Beukelman3, Laura E. Schanberg4, Rayfel Schneider5 and Yukiko Kimura6, 1Pediatric Rheumatology, Hackensack University Medical Center, Hackensack, NJ, 2Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3Pediatric Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Pediatrics, Duke University Medical Center, Durham, NC, 5Pediatric Rheumatology Collaborative Study Group (PRCSG), Cincinnati, OH, Canada, 6Pediatric Rheumatology, Joseph M. Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, NJ

    Background/Purpose: Despite recent advances in identifying effective treatments for systemic Juvenile Idiopathic Arthritis (sJIA), many pediatric rheumatologists continue to use corticosteroids and methotrexate. The Childhood…
  • Abstract Number: 2055 • 2012 ACR/ARHP Annual Meeting

    TEAM-Managed Care of Biological Patients At A Canadian Centre

    Melissa Deamude1, Dawn Heap2, Melanie Kanellos2, Debbie Kislinsky3, Kathy Kislinsky1, Cynthia Mech4, Helena Ross1, Peggy Saldanha3, Lauri Vanstone5, Kathleen Brown6 and William G. Bensen7, 1Dr. William G. Bensen, Rheumatology Health Team, St. Joseph's Hospital Hamilton, Hamilton, ON, Canada, 2Dr. Bensen's Rheumatology Clinic, Hamilton, ON, Canada, 3Dr. William Bensen Rheumatology Clinic, Hamilton, ON, Canada, 4Dr. William G. Bensen, Rheumatology Health Team, Dr. Bensen's Rheumatology Clinic, Hamilton, ON, Canada, 5Dr. William Bensen Rheumatology Biologic Clinic, Rheumatology Health Team, Hamilton, ON, Canada, 6Dr. William Bensen Rheumatology Clinic, Rheumatology Health Team, St. Joseph's Hospital Hamilton, Hamilton, ON, Canada, 7Department of Medicine, Division of Rheumatology, St. Joseph's Hospital and McMaster University, Hamilton, ON, Canada

    Background/Purpose: Managing complex arthritic patients with biologics is exacting and time consuming.  As a result in January 2008 we established a separate biologic clinic with…
  • Abstract Number: 1004 • 2012 ACR/ARHP Annual Meeting

    A Unique Single Nucleotide Polymorphism in the 3’ UTR of the MED29 Gene On Chromosome 19 Is Associated with the Clinical Outcome of Different Biologic Response Modifiers

    Susanne Drynda1, David Leesch2, Marietta Gloetzner2 and Joern Kekow2, 1Clinic of Rheumatology, Univ of Magdeburg, Clinic of Rheumatology, Vogelsang-Gommern, Germany, 2Clinic of Rheumatology, Univ of Magdeburg, Vogelsang-Gommern, Germany

    Background/Purpose: Due to the wide range of highly specific and effective biologic response modifiers that are available today for the treatment of RA it has…
  • Abstract Number: 1839 • 2012 ACR/ARHP Annual Meeting

    The Progression of the Rate of Biologic Initiation in Early Rheumatoid Arthritis Is Constant Over the First 5 Years in the Espoir Cohort

    Stéphanie Emilie1, Cécile Gaujoux-Viala2, Benjamin Granger3, Anne-Christine Rat4, Bernard Combe5 and Bruno Fautrel6, 1Paris 6,Pierre and Marie Curie University, AP-HP, Pitié-Salpêtrière Hospital, Department of Rheumatology, Paris, France, 2Paris 6 – Pierre et Marie Curie University; Rheumatology, Pitié-Salpêtrière Hospital, Paris, France, 3Biostatistics - GRC08-EEMOIS, Université Pierre et Marie Curie - Paris 6 ; AP-HP, Paris, France, 4CHU Nancy, Clinical Epidemiology and Evaluation, Université de Lorraine, Paris Descartes University, APEMAC, EA 4360, Nancy, France, 5Rheumatology, Hopital Lapeyronie, Montpellier, France, 6Rheumatology / GRC08-EEMOIS, APHP-Pitie Salpetriere Hospital / UPMC, Paris, France

    Background/Purpose: The European League Against Rheumatism recommends tight control of rheumatoid arthritis (RA). However, tight control of RA may depend on several factors, including patient…
  • Abstract Number: 782 • 2012 ACR/ARHP Annual Meeting

    Anti-TNF Therapy Slows Radiographic Progression of Ankylosing Spondylitis

    Nigil Haroon1, Robert D. Inman2, Thomas J. Learch3, Michael H. Weisman4, Michael M. Ward5, John D. Reveille6 and Lianne S. Gensler7, 1Medicine/Rheumatology, University Health Network, Toronto Western Research Institute, University of Toronto, Toronto, ON, Canada, 2Dept of Medicine/Rheumatology, Toronto Western Research Institute, University Health Network and University of Toronto, Toronto, ON, Canada, 3Cedars-Sinai, Los Angeles, CA, 4Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 5Bldg 10 CRC Rm 4-1339, NIAMS/NIH, Bethesda, MD, 6Internal Medicine/Rheumatology, Univ of Texas Health Science Center at Houston, Houston, TX, 7Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: The influence of anti-TNF therapy on radiographic progression in ankylosing spondylitis (AS) is not well established. We studied this effect on radiographic progression in…
  • Abstract Number: 1827 • 2012 ACR/ARHP Annual Meeting

    Factors That Impact Work Productivity in the Preserve Trial: A Randomized Controlled Trial of Combination Etanercept-Methotrexate Therapy in Patients with Moderately Active Rheumatoid Arthritis

    Vibeke Strand1, Thomas V. Jones2, Wenzhi Li3, Andrew S. Koenig4 and Sameer Kotak5, 1Adjunct, Division of Immunology / Rheumatology, Stanford University, Portola Valley, CA, 2Inflammation Specialty Care, Pfizer, Inc, Collegeville, PA, 3Pfizer Inc., Collegeville, PA, 4Specialty Care Business Unit, Pfizer Inc., Collegeville, PA, 5Specialty Care, Pfizer Inc., New York, NY

    Background/Purpose: Active joint inflammation and structural damage in patients with rheumatoid arthritis (RA) often result in impaired physical function and ultimately work disability.1,2 Lost productivity…
  • Abstract Number: 762 • 2012 ACR/ARHP Annual Meeting

    Potentially Fatal Pulmonary Complications in Systemic Juvenile Idiopathic Arthritis

    Yukiko Kimura1, Jennifer E. Weiss2, Kathryn L. Haroldson1, Tzielan C. Lee3, Marilynn G. Punaro4, Sheila K. Feitosa de Oliveira5, C. Egla Rabinovich6, Meredith P. Riebschleger7, Jordi Anton8, Peter R. Blier9, Valeria Gerloni10, Melissa M. Hazen11, Elizabeth Kessler12, Karen Onel13, Murray H. Passo14, Robert M. Rennebohm15, Carol A. Wallace16, Patricia Woo17, Nico M. Wulffraat18 and CARRAnet Investigators19, 1Pediatric Rheumatology, JM Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, NJ, 2Pediatric Rheumatology, Joseph M Sanzari Children’s Hospital, Hackensack University Medical Center, Hackensack, NJ, 3Pediatric Rheumatology, Stanford University School of Medicine, Stanford, CA, 4Pediatric Rheumatology, Texas Scottish Rite Hospital, Dallas, TX, 5Pediatric Rheumatology, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil, 6Pediatric Rheumatology, Duke University Medical Center, Durham, NC, 7Pediatric Rheumatology & Health Services Research, University of Michigan, Ann Arbor, MI, 8Rheumatology, Hospital Sant Joan de Deu, Barcelona, Spain, 9Pediatrics, Baystate Children's Hospital, Springfield, MA, 10Pediatric Rheumatology, Gaetano Pini Chair of Rheum, Milan, Italy, 11Division of Immunology, Boston Children's Hospital, Boston, MA, 12Pediatric Rheumatology, Medical College of Wisconsin, Milwaukee, WI, 13Pediatric Rheumatology, University of Chicago Hospitals, Chicago, IL, 14Pediatrics, Medical University of South Carolina, Charleston, SC, 15Pediatric Rheumatology, Alberta Children's Hospital, University of Calgary, Calgary, AB, Canada, 16Pediatrics, Seattle Childrens Hospital, Seattle, WA, 17Division of Infection and Immunity, University College London, London, United Kingdom, 18Pediatric Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 19Durham

    Background/Purpose: Systemic Juvenile Idiopathic Arthritis (sJIA) is characterized by fevers, rash and arthritis, for which IL1 and IL6 inhibitors appear to be effective.  Pulmonary artery…
  • Abstract Number: 1830 • 2012 ACR/ARHP Annual Meeting

    Drugs Are the Major Cost Driver of Rheumatoid Arthritis As Soon As the First Year of the Disease: An Economic Analysis Based On the Espoir Cohort Data

    Bruno Fautrel1, Sandy Lucier2, Georges Haour2, Hassani Maoulida2, Stephanie Harvard1, Alain Saraux3, Xavier Mariette4, Francis Guillemin5, Isabelle Durand-Zaleski2 and Karine Chevreul2, 1Rheumatology / GRC08-EEMOIS, APHP-Pitie Salpetriere Hospital / UPMC, Paris, France, 2APHP - URC Eco, Paris, France, 3Department of rheumatology and unit of immunology (EA 2216), Université Brest Occidentale, Brest, France, 4Rheumatology, Université Paris-Sud, Le Kremlin Bicetre, France, 5Hopitaux de Brabois, Nancy, France

    Background/Purpose: Many studies have explored the economic burden of established RA but few data are available about the determinants of costs in early rheumatoid arthritis…
  • Abstract Number: 692 • 2012 ACR/ARHP Annual Meeting

    A Phase 1 Multicenter, Open-Label Study of MEDI-546, a Human Anti-Type I Interferon Receptor Monoclonal Antibody, in Adults with Scleroderma

    Avram Z. Goldberg1, Thomas D. Geppert2, Elena Schiopu3, Tracy M. Frech4, Vivien M. Hsu5, Robert W. Simms6, Stanford L. Peng7, Yihong Yao8, Nairouz Elgeioushi9, Bing Wang10, Linda Chang11 and Stephen Yoo12, 1Div of Rheumatology, North Shore-LIJ Health System, Lake Success, NY, 2Metroplex Clinical Research Center, LLC, Dallas, TX, 3Rheumatology/Internal Medicine, University of Michigan, Ann Arbor, MI, 4Internal Medicine-Division of Rheumatology, University of Utah School of Medicine, SLC, UT, 5Rheumatology, RWJ Med Schl Scleroderma Prog, New Brunswick, NJ, 6Rheumatology, Boston University School of Medicine, Boston, MA, 7Department of Rheumatology, Benaroya Research Institute at Virginia Mason Medical Center, Seattle, WA, 8Translational Sciences, MedImmune, Gaithersburg, MD, 9Medical Biostatistics, MedImmune, Gaithersburg, MD, 10Clinical Pharmacology and DMPK, Medimmune, Mountain View, CA, 11Translational Sciences, MedImmune, Hayward, CA, 12Clinical Development, MedImmune, Gaithersburg, MD

    Background/Purpose: Type I interferons (IFNs) have been implicated in the pathogenesis of scleroderma. This phase 1 study evaluated safety, pharmacokinetics (PK), pharmacodynamics, and immunogenicity of…
  • « 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 »

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].

Wiley

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

© Copyright 2025 American College of Rheumatology