ACR Meeting Abstracts

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  • Abstract Number: 1374 • 2019 ACR/ARP Annual Meeting

    Real-World Evidence: Infections Among RA Patients Switching from First Biologic DMARD to Another Treatment in the US

    Robin Dore1, Jenya Antonova 2, Huan Huang 3, Lawrence Chang 2, Xin Wang 3 and Mark Genovese 4, 1Private practice, Tustin, CA, 2Gilead Sciences, Foster City, CA, 3IQVIA, Plymouth Meeting, PA, 4Stanford University, Stanford, CA

    Background/Purpose: Infections are common safety events monitored in RA patients.1 ACR guidelines limit the use of live vaccines in patients who are on biologic (b)DMARDs…
  • Abstract Number: 1375 • 2019 ACR/ARP Annual Meeting

    Patient-Reported Outcomes of Upadacitinib versus Adalimumab Use in Patients with Moderately to Severely Active Rheumatoid Arthritis and an Inadequate Response to Methotrexate: 26-Week Analysis of a Phase 3 Study

    Roy Fleischmann1, Martin Bergman 2, Namita Tundia 3, In-Ho Song 4, Jessica Suboticki 4, Yan Song 5 and Vibeke Strand 6, 1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX, 2Drexel University College of Medicine, Stockholm, Sweden, 3AbbVie Inc., North Chicago, IL, 4AbbVie Inc., North Chicago, IL, USA, North Chicago, IL, 5Analysis Group, Inc., Boston, MA, 6Division of Immunology/Rheumatology, Stanford University, Stanford, CA

    Background/Purpose: In patients with active rheumatoid arthritis (RA), 12-week treatment with upadacitinib (UPA) while on background MTX therapy resulted in significant and clinically meaningful improvements…
  • Abstract Number: 1376 • 2019 ACR/ARP Annual Meeting

    Impact of 24- or 26-Week Upadacitinib Monotherapy on Patient-Reported Outcomes in Patients with Moderately to Severely Active Rheumatoid Arthritis and No Prior Use of or an Inadequate Response to Methotrexate: Results from Two Phase 3 Trials

    Vibeke Strand1, Namita Tundia 2, Alan Friedman 3, Heidi Camp 2, Jessica Suboticki 4, Debbie Goldschmidt 5, Catherine Fernan 5 and Martin Bergman 6, 1Division of Immunology/Rheumatology, Stanford University, Stanford, CA, 2AbbVie Inc., North Chicago, IL, 3AbbVie Inc., North Chicago, 4AbbVie Inc., North Chicago, IL, USA, North Chicago, IL, 5Analysis Group, Inc., New York, NY, 6Drexel University College of Medicine, Stockholm, Sweden

    Background/Purpose: Treatment with upadacitinib (UPA) monotherapy, a selective Janus kinase-1 (JAK-1) inhibitor, resulted in significant and clinically meaningful improvements in patient-reported outcomes (PROs) at Week…
  • Abstract Number: 1377 • 2019 ACR/ARP Annual Meeting

    MTX Withdrawal in Patients with RA Who Achieve Low Disease Activity with Tofacitinib Modified-Release 11 Mg Once Daily + MTX: An Assessment of the Impact on the Short Form-36 Patient-Reported Outcome

    Vibeke Strand1, Janet Pope 2, John Woolcott 3, Jose L. Rivas 4, Annette Diehl 3, Shixue Liu 5, David Gruben 6 and Stanley Cohen 7, 1Division of Immunology/Rheumatology, Stanford University, Palo Alto, CA, 2Western University, London, ON, Canada, 3Pfizer Inc, Collegeville, PA, 4Pfizer SLU, Madrid, Spain, 5Pfizer Inc, Shanghai, China (People's Republic), 6Pfizer Inc, Groton, CT, 7Metroplex Clinical Research Center, Dallas, TX

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA. Tofacitinib +/- background MTX has been shown to be an effective treatment…
  • Abstract Number: 1378 • 2019 ACR/ARP Annual Meeting

    High Baseline Serum IL-6 Predicts Increased Sarilumab Treatment Response for Patient Reported Symptoms and Health-Related Quality of Life Among Rheumatoid Arthritis Patients with Inadequate Response to Methotrexate

    Vibeke Strand1, Jerome Msihid 2, Toshio Kimura 3, Anita Boyapati 3, Gregory St John 4 and Wenhui Wei 3, 1Division of Immunology/Rheumatology, Stanford University, Stanford, CA, 2Sanofi, Chilly-Mazarin, France, 3Regeneron Pharmaceuticals, Inc, Tarrytown, NY, 4Regeneron Pharmaceuticals, Inc., Tarrytown, NY

    Background/Purpose: IL-6 is a key cytokine in the pathogenesis of rheumatoid arthritis (RA) and is elevated in serum and synovial fluid of RA patients. However,…
  • Abstract Number: 1379 • 2019 ACR/ARP Annual Meeting

    Glucocorticoid Dose Is Progressively Reduced in Patients with RA Receiving Sarilumab: Results from the Open-Label EXTEND Study

    Roy Fleischmann1, Carlo Selmi 2, Miguel Angel González-Gay 3, Hubert van Hoogstraten 4, Owen Hagino 4, Tejasweeni Rajput 5, Gregory St John 6, Frank Buttgereit 7 and Mark Genovese 8, 1Metroplex Clinical Research Center and University of Texas Southwestern Medical Center, Dallas, TX, 2Humanitas Research Hospital, University of Milan, Milan, Italy, 3Universidad de Cantabria and IDIVAL, Hospital Universitario Marqués de Valdecilla, Santander, Spain, 4Sanofi, Bridgewater, NJ, 5Cytel, Mumbai, India, 6Regeneron Pharmaceuticals, Inc., Tarrytown, NY, 7Charité-Universitätsmedizin Berlin, Berlin, Germany, 8Stanford University, Stanford, CA

    Background/Purpose: EXTEND (NCT01146652) is a long-term, open-label extension (OLE) study of sarilumab for the treatment of RA. This post hoc analysis assessed changes in oral…
  • Abstract Number: 1380 • 2019 ACR/ARP Annual Meeting

    Patient Characteristics, Treatment Patterns, and Treatment Persistency in Biologic DMARD-Experienced Rheumatoid Arthritis Patients in a US RA Registry

    Robin Dore1, Jenya Antonova 2, Leslie Harrold 3, Lawrence Chang 2, Emily Scherer 4, Angel Cronin 5, Kelechi Emeanuru 5 and Joel Kremer 6, 1Private practice, Tustin, CA, 2Gilead Sciences, Foster City, CA, 3Corrona, LLC and University of Massachusetts Medical School, Worcester, MA, 4Corrona, LLC, Cambridge, MA, 5Corrona, LLC, Waltham, MA, 6Albany Medical College and The Center for Rheumatology; Corrona, LLC, Albany, NY

    Background/Purpose: Multiple treatment options are available for patients with RA. ACR guidelines recommend initiating treatment with a conventional synthetic DMARD (csDMARD). If a patient fails…
  • Abstract Number: 1381 • 2019 ACR/ARP Annual Meeting

    High Serum IgA and High Proportion of Activated Th17 and Activated Treg Cells Are Predictive Biomarkers for Remission Achievement with Abatacept in Patients with Early, Seropositive Rheumatoid Arthritis

    Jun Inamo1, Yuko Kaneko 2, Jun Kikuchi 3 and Tsutomu Takeuchi 4, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Tokyo, Japan, 2Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku, Tokyo, Japan, 3Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan, 4Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: Abatacept (ABT) is a soluble fusion protein, which links cytotoxic T-lymphocyte-associated protein 4 to the modified Fc portion of IgG1. Seropositivity and a shorter…
  • Abstract Number: 1382 • 2019 ACR/ARP Annual Meeting

    The Efficacy of Low Dose Prednisone for Remission Induction in Newly Diagnosed Rheumatoid Arthritis Patients

    Jacob Greenmyer 1, John Stacy 1, James Beal 2, Abe Sahmoun 2 and Erdal Diri1, 1University of North Dakota, School of Medicine Health Sciences, Minot, ND, 2University of North Dakota, School of Medicine Health Sciences, Grandforks, ND

    Background/Purpose: Glucocorticoids (GCs) are commonly used in RA patients as remission induction monotherapy or as bridging therapy when starting DMARD/biologic therapy.  Despite the ubiquity of…
  • Abstract Number: 1383 • 2019 ACR/ARP Annual Meeting

    Glucocorticoid Tapering in Monthly 1-mg Decrements Does Not Result in Clinically Manifest Adrenal Insufficiency in Patients with Rheumatoid Arthritis: Learnings from a Phase 3/4 Study

    Frank Buttgereit1, J. Michael Nebesky 2, Gerd Burmester 3, Corrado Bernasconi 2, Markus R. John 2 and Marc Y. Donath 4, 1Charité-Universitätsmedizin Berlin, Berlin, Germany, 2F. Hoffmann-La Roche, Basel, Switzerland, 3Charité—University Medicine Berlin, Berlin, Germany, 4University Hospital Basel, Basel, Switzerland

    Background/Purpose: Systemic glucocorticoids (GCs) are used to treat serious inflammatory diseases but are associated with adverse events. Guidelines recommend tapering GCs to the lowest possible…
  • Abstract Number: 1384 • 2019 ACR/ARP Annual Meeting

    Duration of Oral Corticosteroid Therapy Does Not Change with the Addition of a Parenteral Injection: Results from a Real-World Canadian Early RA Cohort

    Kathleen M Andersen1, Orit Schieir 2, Marie-France Valois 3, Susan J. Bartlett 4, Louis Bessette 5, Gilles Boire 6, Glen Hazlewood 7, Carol Hitchon 8, Edward Keystone 9, Janet Pope 10, Diane Tin 11, Carter Thorne 12, Vivian Bykerk 13 and Canadian Early Arthritis Cohort (CATCH) Investigators 14, 1Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health,, Baltimore, MD, 2University of Toronto, Montreal, Canada, 3McGill University, Montreal, Canada, 4McGill University, Montreal, QC, Canada, 5Laval University, Quebec City, QC, Canada, 6Sherbrooke University, Sherbrooke, QC, Canada, 7University of Calgary, Calgary, Canada, 8University of Manitoba, Winnipeg, Canada, 9Mount Sinai Hospital and University of Toronto, Toronto, ON, Canada, 10Western University, London, ON, Canada, 11Southlake Regional Health Centre, Newmarket, Canada, 12Southlake Regional Health Centre, Newmarket, ON, Canada, 13Hospital for Special Surgery, New York City, NY, 14Canadian Early Arthritis Cohort (CATCH) Study, Toronto, Canada

    Background/Purpose: Synthetic glucocorticoids (steroids) are recommended for and commonly used in rheumatoid arthritis (RA) as initial “bridge therapy”, acting to rapidly reduce the inflammatory response…
  • Abstract Number: 1385 • 2019 ACR/ARP Annual Meeting

    Discontinuation of Oral Glucocorticoid After Initiation of Biological DMARDs Due to a Higher Dose of Methotrexate; A Retrospective Observational Study Based on Data from a Japanese Multicenter Registry Study

    Mochihito Suzuki1, Toshihisa Kojima 2, Nobunori Takahashi 2, Shuji Asai 2 and Naoki Ishiguro 2, 1Nagoya University Graduate School of Medicine, Nagoya, Japan, 2Department of Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan

    Background/Purpose:  In the treatment of rheumatoid arthritis (RA), glucocorticoid that provide anti-inflammatory effects is an important drug. We recommend discontinuing of glucocorticoid as soon as…
  • Abstract Number: 1386 • 2019 ACR/ARP Annual Meeting

    Association Between Baseline Anti-citrullinated Protein Antibody Status and Response to Abatacept or Non-TNF Inhibitor Therapy in Patients with RA: Results from a US National Observational Study

    Leslie Harrold1, Ying Shan 2, Sabrina Rebello 2, Lin Guo 2, Sean Connolly 3, Joe Zhuo 3, Sheila Kelly 3 and Thomas Lehman 3, 1University of Massachusetts and Corrona, LLC, Waltham, MA, 2Corrona, LLC, Waltham, MA, 3Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: In a US national observational study conducted in a clinical practice setting, patients who were positive (+) for anti-cyclic citrullinated peptide (CCP) antibodies at…
  • Abstract Number: 1387 • 2019 ACR/ARP Annual Meeting

    Low Probability of Clinical Worsening Following Switching Biologic DMARD in Patients with RA and Partial Response to Adalimumab

    Jeffrey Curtis1, Daniel Aletaha 2, Gerd Burmester 3, Kerri Ford 4, Hubert van Hoogstraten 5, Henry Leher 6, Karthinathan Thangavelu 7 and Vivian Bykerk 8, 1University of Alabama at Birmingham, Birmingham, AL, 2Medical University of Vienna, Vienna, Austria, 3Charité—University Medicine Berlin, Berlin, Germany, 4Sanofi Genzyme, Bridgewater, NJ, 5Sanofi, Bridgewater, NJ, 6Regeneron Pharmaceuticals, Inc, Tarrytown, NY, 7Sanofi Genzyme, Boston, MA, 8Hospital for Special Surgery, New York City, NY

    Background/Purpose: Guidelines recommend adjusting therapy in patients with RA who fail to reach low disease activity or remission. Partial responders to a TNF inhibitor may…
  • Abstract Number: 1388 • 2019 ACR/ARP Annual Meeting

    The Association Between Treatment of Abatacept or Other Target Disease-Modifying Anti-rheumatic Drugs and Type 2 Diabetes Mellitus (T2DM)-Related Healthcare Resource Utilization and Costs in Commercially Insured Rheumatoid Arthritis Patients with T2DM

    Qian Xia 1, Xue Han2, Ying Bao 1, Vardhaman Patel 3, Varshini Rajagopalan 4 and Francis Lobo 2, 1Bristol-Myers Squibb, Lawrenceville, NJ, 2Bristol-Myers Squibb Company, Princeton, NJ, 3Bristol-Myers Squibb, New York City, NY, 4Mu-Sigma, Bengaluru, India

    Background/Purpose: Type 2 diabetes mellitus (T2DM)-related complications are costly, and there is lack of information regarding the comparative impact of target disease-modifying anti-rheumatic drugs (tDMARDs)…
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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.

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