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  • Abstract Number: 513 • 2014 ACR/ARHP Annual Meeting

    Analysis of Shoulder Joint Destruction in Rheumatoid Arthritis Patients Treated with Biologics

    Yukio Yonemoto, Koichi Okamura, Tetsuya Kaneko, Chisa Okura and Kenji Takagishi, Department of Orthopaedic Surgery, Gunma University Graduate School of Medicine, Maebashi, Japan

    Background/Purpose The assessment of joint destruction in rheumatoid arthritis (RA) patients being treated with biologics is normally mainly carried out for small joints. There are…
  • Abstract Number: 514 • 2014 ACR/ARHP Annual Meeting

    Methotrexate Reduces the Frequency of Prediabetes in Patients with Rheumatoid Arthritis or Psoriatic Arthritis

    Katja Perdan-Pirkmajer1, Sergej Pirkmajer2, Alojzija Hocevar1, ŽIga Rotar1, Natasa Gaspersic1, Sonja Praprotnik1, Matija Tomsic3 and Ales Ambrozic1, 1Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia, 2Institute of Pathophysiology, Faculty of Medicine Ljubljana, Ljubljana, Slovenia, 3Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia, Ljubljana, Slovenia

    Background/Purpose Rheumatoid arthritis (RA) and psoriatic arthritis (PsA) are associated with an increased risk of diabetes mellitus (DM). Disease-modifying anti-rheumatic drugs, including methotrexate (MTX), may…
  • Abstract Number: 515 • 2014 ACR/ARHP Annual Meeting

    Dosing of Intravenous Tocilizumab in a Real-World Setting—Analyses from a US RA Registry

    Dimitrios A. Pappas1, Ani John2, Jeffrey R. Curtis3, George W. Reed4,5, Chitra Karki6, Robert Magner5, Joel M. Kremer7, Ashwini Shewade2 and Jeffrey D. Greenberg6,8, 1Columbia University, New York, NY, 2Genentech, Inc, South San Francisco, CA, 3University of Alabama at Birmingham, Birmingham, AL, 4Corrona, LLC., Southborough, MA, 5University of Massachusetts Medical School, Worcester, MA, 6Corrona, LLC, Southborough, MA, 7Albany Medical College and The Center for Rheumatology, Albany, NY, 8NYU School of Medicine, New York, NY

    Background/Purpose: In the US, the recommended starting dose of intravenous tocilizumab (TCZ) in combination with DMARDs or as monotherapy is 4 mg/kg every 4 weeks…
  • Abstract Number: 505 • 2014 ACR/ARHP Annual Meeting

    A Structured Approach for Comparative Benefit-Risk Assessment of Rituximab for the Treatment of Rheumatoid Arthritis

    Ani John1, George Quartey1, Patricia B. Lehane2, Nicole Mairon3, Michael Schulte3, Ashwini Shewade1, Carol Chung1 and Dominic Borie1, 1Genentech, Inc, South San Francisco, CA, 2Roche Products Ltd, Welwyn Garden City, United Kingdom, 3F. Hoffmann-La Roche Ltd, Basel, Switzerland

    Background/Purpose: Rituximab in combination with methotrexate (MTX) is indicated for the treatment of adult patients with moderate to severe active rheumatoid arthritis (RA) who have…
  • Abstract Number: 484 • 2014 ACR/ARHP Annual Meeting

    Reactivation of Hepatitis B Virus in Patients with Rheumatoid Arthritis after Anti-TNF Therapy

    Seung Min Jung1, Hong Ki Min1, Jung Hee Koh1, Jin Young Kang1, Jennifer Lee1, Seung-Ki Kwok2, Ji Hyeon Ju1, Hyeok-Jae Ko3, Kyung-Su Park4, Ho-Youn Kim1 and Sung-Hwan Park1, 1Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea, 2Division of Rheumatology, Department of Internal Medicine, St. Mary’s hospital, The Catholic University of Korea, Seoul, South Korea, 3Division of Rheumatology, Department of Internal Medicine, Daejeon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Daejeon, South Korea, 4Internal Medicine, St. Vincent Hospital, SuWon Gyeonggi-do, South Korea

    Background/Purpose: Anti-TNF therapy was known to increase the risk of certain infection. There are only limited data about the reactivation of hepatitis B virus (HBV)…
  • Abstract Number: 485 • 2014 ACR/ARHP Annual Meeting

    Incidence of Clinical and Serological Lupus-like Disease during Anti-Tnfα-Treatment – a Two-Year Prospective Study in an Interdisciplinary Patient Cohort

    Simon Julius Winkelmann1, Rainald A. Zeuner1, Dörte Schuldt1, Johannes Bethge1, Ulrich Mrowietz2, Matthias Laudes1, Stefan Schreiber1 and Johann Schroeder1, 11st Medical Dept, University of Kiel, Kiel, Germany, 2Dermatology, Univ Schleswig-Holstein, Kiel, Germany

    Background/Purpose: TNFα-Inhibitors are the most widely used biological agents in rheumatic conditions or other chronic inflammatory diseases. Over the last ten years, the occurrence of…
  • Abstract Number: 483 • 2014 ACR/ARHP Annual Meeting

    Risk of HBV Reactivation in Rheumatoid Arthritis Patients Undergoing Treatment with Newer Biological Dmards, Tocilizumab and Abatacept: A Single-Center Real Life Experience

    Francesca De Nard1, Vittorio Grosso2, Monica Todoerti3, Carlomaurizio Montecucco4 and Roberto Caporali5, 1Division of Rheumatology, University of Pavia, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy, 2Division of Rheumatology, University of Pavia, Foundation IRCCS Policlinico S. Matteo, Pavia, Italy, 3Rheumatology, University of Pavia, IRCCS Policlinico S. Matteo Foundation, Pavia, Italy, 4Rheumatology and Translational Immunology Research Laboratories (LaRIT), Division of Rheumatology, IRCCS Policlinico S.Matteo Foundation/University of Pavia, Pavia, Italy, 5Division of Rheumatology, Rheumatology and Translational Immunology Research Laboratories (LaRIT), Division of Rheumatology, IRCCS Policlinico S.Matteo Foundation/University of Pavia, Pavia, Italy

    Background/Purpose HBV infection represents a major issue in patients with rheumatoid arthritis (RA) undergoing biological disease-modifying anti-rheumatic drugs (bDMARDs) (1). While the risk of hepatitis…
  • Abstract Number: 482 • 2014 ACR/ARHP Annual Meeting

    Incidence of Opportunistic Infections in Rheumatoid Arthritis Treated with Biological Agents

    Alejandro Gomez-Gomez1,2, Zulema Rosales1,2, Leticia Leon2, Juan A Jover2, Luis Rodriguez-Rodriguez2 and Lydia Abasolo2, 1Rheumatology, Hospital Clinico San Carlos, Madrid, Spain, 2Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain

    Background/Purpose With the expanding use of Biological Agents (BA), in particular TNF inhibitors, opportunistic infections (OI) are a major concern in Rheumatology. Our purposes were…
  • Abstract Number: 481 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Etanercept in Rheumatoid Arthritis Patients over 75 Years Old

    Satoru Kodama, Satoshi Ito, Akira Murasawa, Kiyoshi Nakazono and Daisuke Kobayashi, Niigata Rheumatic Center, Shibata, Japan

    Background/Purpose Early introductions of biologics in early rheumatoid arthritis (RA) patients are well documented, but there are few reports of biologics use in established elderly…
  • Abstract Number: 480 • 2014 ACR/ARHP Annual Meeting

    Serious Infection Risk By Treatments and Types in Patients with RA

    Kaleb Michaud1,2, Sofia Pedro1, Andre Kalil3, Ted R. Mikuls4 and Frederick Wolfe1, 1National Data Bank for Rheumatic Diseases, Wichita, KS, 2Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 3Infectious Diseases, University of Nebraska Medical Center, Omaha, NE, 4University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: Recent studies provide conflicting results on the impact of DMARDs on the risk of serious infections for patients with RA. We examined these infection…
  • Abstract Number: 479 • 2014 ACR/ARHP Annual Meeting

    Long Term Safety of Intravenous Golimumab and Comparison with Subcutaneous Golimumab in Rheumatoid Arthritis:  Results through 2 Years

    Rene Westhovens1, Edward C. Keystone2, Clifton O. Bingham III3, Elizabeth C. Hsia4,5, Lilianne Kim4, Yiying Zhou4, Alan M. Mendelsohn6 and Michael E. Weinblatt7, 1Rheumatology, University Hospital KU Leuven, Leuven, Belgium, 2Department of Medicine, Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada, 3Johns Hopkins University, Baltimore, MD, 4Janssen Research & Development, LLC., Spring House, PA, 5University of Pennsylvania, Philadelphia, PA, 6Immunology, Janssen Research & Development, LLC., Spring House, PA, 7Division of Rheumatology & Immunology, Brigham and Women's Hospital, Boston, MA

    Long Term Safety of Intravenous Golimumab and Comparison with Subcutaneous Golimumab in Rheumatoid Arthritis:  Results through 2 Years Background/Purpose:   To describe the safety profile…
  • Abstract Number: 498 • 2014 ACR/ARHP Annual Meeting

    Patient Experience with Initiation of SQ and Oral MTX

    Jeffrey R. Curtis1, David Mackey2, Noam Gerber3, Aseem Bharat1, Lang Chen4, Fenglong Xie5, Ben Nowell3, Kenneth G. Saag6 and Seth Ginsberg7, 1University of Alabama at Birmingham, Birmingham, AL, 2Clinical Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Creaky Joints/Global Healthy Living Foundation, Upper Nyack, NY, 4Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 6Immunology & Rheumatology, The University of Alabama at Birmingham, Birmingham, AL, 7CreakyJoints/Global Healthy Living Foundation, Upper Nyack, NY

    Background/Purpose Methotrexate is the anchor drug used for the treatment of rheumatoid arthritis (RA). Despite its prominent position in RA therapeutics, its real-world effectiveness may…
  • Abstract Number: 497 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety Study of a Sequential Therapy of Tocilizumab and, If Initially Inadequately Responded to Tocilizumab, Followed By Rituximab in Patients with Rheumatoid Arthritis and Inadequate Response to Traditional Disease Modifying Anti-Rheumatic Drugs

    Thomas Dörner1, Hans-Peter Tony2, Gerd Burmester1, Hendrik Schulze-Koops3, Jörg Kaufmann4, Peter Kästner5, Herbert Kellner6, Reiner Kurthen7, Sylke Wagner8, Marvin A. Peters9 and Christoph Iking-Konert10, 1Charité - Universitätsmedizin Berlin, Berlin, Germany, 2University Clinic Wuerzburg, Wuerzburg, Germany, 3University Clinic Munich, Munich, Germany, 4Rheumatology Practice, Ludwigsfelde, Germany, 5MVZ Out-patient Rheumatogy Unit Erfurt, Erfurt, Germany, 6Specialist Practice for Rheumatology and Gastroenterology, Munich, Germany, 7Rheumatology Practice, Aachen, Germany, 8Practice for Internal Medicine specialized in Rheumatology, Halle, Germany, 9Roche Pharma AG, Grenzach-Wyhlen, Germany, 10University Clinic Hamburg-Eppendorf, Hamburg, Germany

    Background/Purpose: The MIRAI study evaluated a sequential exposure to 2 defined biologics under rigorous study conditions within a homogeneous population of biological naïve patients (pts)…
  • Abstract Number: 496 • 2014 ACR/ARHP Annual Meeting

    Efficacy and Safety of Induction Therapy for Rheumatoid Arthritis with Simultaneous Administration of Methotrexate and Low-Dose Tacrolimus: A Retrospective Study

    Takashi Nakanishi1, Hideyuki Horikoshi1, Reiko Takahashi1, Kanami Tongu2, Junko Nishioka2, Fumihiko Kimura3, Yuichi Nishioka2 and Kenji Itoh1, 1Division of Rheumatology, Department of Internal Medicine, National Defense Medical College, Tokorozawa, Japan, 2Nishioka Clinic for Rheumatic Diseases and Allergic Diseases, Kofu, Japan, 3National Defense Medical College, Tokorozawa, Japan

    Background/Purpose Additional administration of low-dose tacrolimus (LD-TAC) at 0.5–1.0 mg daily was reported to be quite effective for rheumatoid arthritis (RA) patients with inadequate response…
  • Abstract Number: 495 • 2014 ACR/ARHP Annual Meeting

    Discontinuation of Biologics in Patients with Rheumatoid Arthritis after Achieving Low-Activity Disease Status

    Moeko Ochiai1, Eri Sato1, Eiichi Tanaka1, Eisuke Inoue1, Ayako Nakajima1, Shigeki Momohara2, Atsuo Taniguchi2 and Hisashi Yamanaka2, 1Rheumatology, Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan, 2Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan

    Background/Purpose: Several clinical trials have reported bio-free remission or discontinuation of biologic DMARDs; however, these findings have not been confirmed in a real-world setting. The…
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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.).

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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