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  • Abstract Number: 1525 • 2018 ACR/ARHP Annual Meeting

    Effect of JAK-Inhibitor Versus Bdmards on Quality of Life in Rheumatoid Arthritis : A Meta Analysis of Randomized Controlled Trials

    Mamadaly Boudhabhay1, Thomas Barnetche2 and Pascale Vergne-Salle3, 1CHU de Limoges, Limoges, France, 2Rheumatology Department, FHU ACRONIM, Bordeaux University Hospital, Bordeaux, France, 3Rheumatology, CHU de Limoges, Limoges, France

    Background/Purpose: Recent studies comparing JAK-inhibitors (Jak-i) and adalimumab seem to show a better efficacy of JAK-i on patient-reported outcomes in rheumatoid arthritis (RA). As there…
  • Abstract Number: 1526 • 2018 ACR/ARHP Annual Meeting

    Baseline Characteristics and Outcomes in Patients with Anemia in Clinical Studies of Tofacitinib

    Burkhard Moeller1, Axel Finckh2, Jose Maria Alvaro-Gracia3, Godehard Scholz1, Daniel Aletaha4, Francesca Biondo5, Sander Strengholt6, Jose L Rivas7, Carol A Connell8 and Harry Shi9, 1Inselspital-University Hospital, Bern, Switzerland, 2University Hospital of Geneva, Geneva, Switzerland, 3Hospital Universitario de La Princesa, Madrid, Spain, 4Medical University of Vienna, Vienna, Austria, 5Pfizer Inc, Rome, Italy, 6Pfizer Inc, Capelle aan den IJssel, Netherlands, 7Pfizer SLU, Madrid, Spain, 8Pfizer Inc, Groton, CT, 9Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA. The purpose of this study is to describe the profile of patients…
  • Abstract Number: 1527 • 2018 ACR/ARHP Annual Meeting

    Tofacitinib Improves Left Ventricular Mass and Cardiac Output in Rheumatoid Arthritis Patients with Chronic Heart Failure

    Kensuke Kume1, Kanzo Amano2, Susumu Yamada3, Toshikatsu Kanazawa3 and Kazuhiko Hatta4, 1Rheumatology, Hiroshima Clinic, Hiroshima, Japan, 2rheumatology., hiroshima clinic, Hiroshima, Japan, 3rheumatology, hiroshima clinic, hiroshima, Japan, 4Rheumatology, Hatta Clinic, Kure, Japan

    Background/Purpose: Rheumatologists need to develop primary and secondary prevention strategies for cardiovascular disease (CVD) in rheumatoid arthritis (RA) patients. We reported tofacitinib (Tofa) (with or…
  • Abstract Number: 1528 • 2018 ACR/ARHP Annual Meeting

    Unique Changes in Hemoglobin with Sarilumab Versus Adalimumab Are Independent of Better Disease Control in Patients with Rheumatoid Arthritis (RA)

    Gerd R. Burmester1, Owen Hagino2, Qunming Dong3, Marina Stanislav4, Antonio Gomez-Centeno5, Carlo Selmi6, Tom W.J. Huizinga7, Erin Mangan8, Cem Gabay9 and Mark C. Genovese10, 1Charité – University Medicine Berlin, Free University and Humboldt University Berlin, Berlin, Germany, 2Sanofi Genzyme, Bridgewater, NJ, 3Sanofi, Bridgewater, NJ, 4Scientific Research Institute of Rheumatology, Russian Academy of Medical Sciences, Moscow, Russian Federation, 5Corporació Sanitària Parc Taulí, Barcelona, Spain, 6Rheumatology and Clinical Immunology Unit, Humanitas Research Hospital, Rozzano (MI), Italy, 7Leiden University Medical Center, Leiden, Netherlands, 8Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 9University Hospitals of Geneva, Geneva, Switzerland, 10Stanford University Medical Center, Palo Alto, CA

    Background/Purpose: Anemia (WHO criteria: Hemoglobin [Hb] levels <12.0 g/dL [females] or <13.0 g/dL [males]) is a common finding associated with increased joint inflammation in patients…
  • Abstract Number: 1529 • 2018 ACR/ARHP Annual Meeting

    Long-Term, Real-World Safety of Adalimumab in Rheumatoid Arthritis

    Leslie R. Harrold1,2, Jenny Griffith3, Heather J Litman4, Bernice Gershenson1, Syed Islam3, Christine J Barr2, Dianlin Guo3, Patrick Zueger5, Jonathan Fay3 and Jeffrey Greenberg2,6, 1University of Massachusetts Medical School, Worcester, MA, 2Corrona, LLC, Waltham, MA, 3AbbVie, Inc., North Chicago, IL, 4Corrona LLC, Waltham, MA, 5AbbVie Inc., North Chicago, IL, 6New York University School of Medicine, New York, NY

    Background/Purpose: The incidence of adverse events (AE) among rheumatology medication users has not been well documented in real-world disease registry datasets in the US.  We…
  • Abstract Number: 1530 • 2018 ACR/ARHP Annual Meeting

    CRP Changes during Bacterial Infections in Baricitinib-Treated Patients with RA

    Oliver Hendricks1, Stavros Chrysidis2, Jens Gerwien3, Chadi Saifan3, Francesco de Leonardis3, Pedro Lopez-Romero3, Jinglin Zhong4, Kevin Winthrop5 and Josef S. Smolen6, 1King Chr.Xs Rheumatology Hospital, Graasten, Denmark, 2Rheumatology Department Sydvestjysk Sygehus, Esbjerg, Denmark, 3Eli Lilly and Company, Indianapolis, IN, 4Quintiles, Rockville, MD, 5Oregon Health Sciences University, Portland, OR, 6Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Baricitinib (BARI) is a selective inhibitor of Janus kinase 1/2, modulating responses to inflammatory cytokines, e.g. IL-6 or IFNs1. During acute inflammation, including those…
  • Abstract Number: 1531 • 2018 ACR/ARHP Annual Meeting

    Tofacitinib Show Similar Retention When Used with and without Methotrexate. Analysis from the Rhumadata® Clinical Database and Registry

    Denis Choquette1, Louis Bessette2, Jacques Brown2, Boulos Haraoui1, Frédéric Massicotte1, Jean-Pierre Pelletier1, Jean-Pierre Raynauld1, Marie-Anaïs Rémillard1, Diane Sauvageau1, Angèle Turcotte2, Édith Villeneuve1 and Louis Coupal1, 1Rheumatology, Institut de Recherche en Rhumatologie de Montréal (IRRM), Montréal, QC, Canada, 2Rheumatology, Centre de l'Ostéoporose et de Rhumatologie de Québec (CORQ), Québec, QC, Canada

    Background/Purpose: Tofacitinib (TOFA), a targeted synthetic DMARD has recently appeared on the Canadian market. It is an oral agent, targeting the JAK 1 and JAK…
  • Abstract Number: 1532 • 2018 ACR/ARHP Annual Meeting

    Impact of Immunogenicity on Clinical Efficacy and Administration Related Reaction in TNF Inhibitors: A Pooled-Analysis from Three Biosimilar Studies in Patients with Rheumatoid Arthritis

    Paul Emery1, Michael E Weinblatt2, Josef S. Smolen3, Edward C. Keystone4, Mark C. Genovese5, Jiri Vencovsky6, Jonathan Kay7, Evelyn Hong8 and Jeehoon Ghil8, 1University of Leeds and NIHR Leeds Biomedical Research Centre, Leeds, United Kingdom, 2Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 3Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria, 4Mount Sinai Hospital, Toronto, ON, Canada, 5Stanford University Medical Center, Palo Alto, CA, 6Institute of Rheumatology and Department of Rheumatology, 1st Faculty of Medicine, Charles University, Czech Republic, Prague 2, Czech Republic, 7UMass Memorial Medical Center and University of Massachusetts Medical School, Worcester, MA, 8Samsung Bioepis Co., Ltd., Incheon, Korea, Republic of (South)

    Background/Purpose: SB4, SB2, and SB5 are biosimilars of reference etanercept, infliximab, and adalimumab, respectively. The phase III randomized, double-blind clinical studies comparing the efficacy and…
  • Abstract Number: 1533 • 2018 ACR/ARHP Annual Meeting

    Simulating Population Disability Outcomes for Alternative Treatment Pathways in Patients with Active Rheumatoid Arthritis

    Josephine Mauskopf1, Mahdi Gharaibeh2, David Wamble1, David H. Collier2, Bradley S. Stolshek2 and Eric L. Matteson3, 1RTI Health Solutions, Research Triangle Park, NC, 2Amgen Inc., Thousand Oaks, CA, 3Division of Rheumatology, Mayo Clinic College of Medicine and Science, Rochester, MN

    Background/Purpose:  Rheumatoid arthritis (RA) is a chronic, systemic inflammatory disorder that causes joint pain and swelling, bone erosions, and deformity.  This debilitating disease can severely…
  • Abstract Number: 1534 • 2018 ACR/ARHP Annual Meeting

    Comparative Risk of Diabetes Mellitus in Rheumatoid Arthritis Patients Treated with Different Biologics- a Cohort Study

    Rishi J. Desai1, Sara Dejene2, Yinzhu Jin2, Jun Liu3 and Seoyoung C. Kim2, 1Division of Pharmacoepidemiology and Pharmacoeconimics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Brigham and Women's Hospital, Boston, MA, 3Division of Pharmacoepidemiology and Pharmacoeconomics, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Patients with rheumatoid arthritis (RA) often develop diabetes mellitus (DM), potentially due to aggravated systemic inflammation. Reducing inflammation with disease-modifying antirheumatic drugs (DMARD) may…
  • Abstract Number: 1535 • 2018 ACR/ARHP Annual Meeting

    Enhancing Patient Ability to Process and Use Information about Medication Risks and Benefits

    Genevieve Hickey1, Caprice Hunt1, Molly Keebler2, Delesha M. Carpenter3, Elizabeth (Blair) Solow4, Valerie Reyna5, W. Benjamin Nowell6, Cynthia Edmonds1, Kimberlee O'Neill1 and Susan J. Blalock1, 1Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, 2Center for BrainHealth, University of Texas Dallas, Dallas, TX, 3Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Asheville, NC, 4UT Southwestern Rheumatology, Dallas, TX, 5Cornell University, Ithica, NY, 6Global Healthy Living Foundation, Upper Nyack, NY

    Background/Purpose: Guidelines for the treatment of rheumatoid arthritis (RA) underscore the importance of an early and targeted approach to control inflammation. However, patients are often…
  • Abstract Number: 1536 • 2018 ACR/ARHP Annual Meeting

    Mean Platelet Volume Changes with Baricitinib Indicate Reduced New Platelet Production in Baricitinib-Treated Rheumatoid Arthritis Patients

    Jon T. Giles1, Michael T. Nurmohamed2, Henry M. Rinder3, Venkatesh Krishnan4, Brenda J. Crowe4, Chadi Saifan4 and Thomas Dörner5, 1Columbia University, New York, NY, 2VU University Medical Center, Amsterdam, Netherlands, 3Yale University School of Medicine, New Haven, CT, 4Eli Lilly and Company, Indianapolis, IN, 5Charité Universitätsmedizin Berlin and Deutsches Rheuma-Forschungszentrum (DRFZ), Berlin, Germany

    Background/Purpose: Transient increases in circulating platelets were observed in patients with RA treated with baricitinib, an oral selective Janus kinase 1/2 inhibitor, approved for the…
  • Abstract Number: 1537 • 2018 ACR/ARHP Annual Meeting

    Frequency and Duration of Early Non-Serious Adverse Events in Rheumatoid Arthritis Patients Treated with Tofacitinib 5 Mg Twice Daily As Monotherapy and Combination Therapy

    Ara Dikranian1, Jürgen Wollenhaupt2, Valderilio F Azevedo3, Louis Bessette4, David Gold5, Jose L Rivas6, Harry Shi7, Lisy Wang8, John Woolcott7, Andrea Shapiro9 and Peter Nash10, 1Cabrillo Center for Rheumatic Disease, San Diego, CA, 2Schön Klinik Hamburg-Eilbek Teaching Hospital of the University of Hamburg, Hamburg, Germany, 3Universidade Federal do Paraná, Curitiba, Brazil, 4Laval University, Kirkland, QC, Canada, 5Pfizer Canada, Montreal, QC, Canada, 6Pfizer SLU, Madrid, Spain, 7Pfizer Inc, Collegeville, PA, 8Pfizer Inc, Groton, CT, 9Pfizer Inc, Peapack, NJ, 10University of Queensland, Brisbane, Australia

    Background/Purpose: Tolerability remains ill-defined in clinical trials and most commonly refers to non-serious adverse events (AEs) that may impact patient (pt) satisfaction and adherence to…
  • Abstract Number: 1538 • 2018 ACR/ARHP Annual Meeting

    Moderate Adverse Drug Reactions Due to Disease Modifying Drugs in a Cohort of Patients with Incident Rheumatoid Arthritis

    Lydia A Alcazar1, Dalifer Freites Núñez1, Isabel Hernández-Rodríguez2, Judit Font Urgelles2, Pia Mercedes Lois2, Benjamín Fernández-Gutiérrez2, Juan A Jover Jover1 and Zulema Rosales Rosado1,2, 1Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain, 2Rheumatology, Hospital Clínico San Carlos, Madrid, Spain

    Background/Purpose: In rheumatology, we are aware of the possibility to develop adverse drug reactions (ADR) to the widely used Disease Modifying Drugs (DMARD). We are…
  • Abstract Number: 1539 • 2018 ACR/ARHP Annual Meeting

    Safety of Methotrexate and Leflunomide Combination Therapy in the Treatment of Rheumatoid Arthritis

    María Badilla1, Nicia Moldenhauer2, Diego Neira3, Luis Muñoz4 and Oscar Neira1, 1Rheumatology Section., Hospital del Salvador, Universidad de Chile., Santiago, Chile, 2Rheumatology Section, Hospital del Salvador, Universidad de Chile, Santiago, Chile, 3Internal Medicine Departament, Hospital del Salvador, Universidad de Chile, Santiago, Chile, 4Pharmacy Department, Hospital del Salvador, Santiago, Chile

    Background/Purpose: Best treatment of Rheumatoid Arthritis (RA) requires to begin early, with a tight control, including nonsteroidal anti-inflammatory drugs (NSAIDs), steroids, disease-modifying antirheumatic drugs (DMARDs)…
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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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