ACR Meeting Abstracts

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Abstracts tagged "Psoriatic arthritis"

  • Abstract Number: 681 • 2018 ACR/ARHP Annual Meeting

    Identification of Treatment Naïve Patients with Psoriatic Arthritis Who Will Require a TNF Inhibitor

    Dan Gromer1, Laura C. Coates2, Oliver FitzGerald3, Blanca Himes4, Philip Helliwell5 and Alexis Ogdie6, 1University of Pennsylvania, Medical Student, Philadelphia, PA, 2University of Oxford, Oxford, United Kingdom, 3Department of Rheumatology, St Vincent's University Hospital and Conway Institute, University College Dublin, Ireland, Dublin, Ireland, 4Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA, 5LIMM, Section of Musculoskeletal Disease, University of Leeds, Leeds, United Kingdom, 6Medicine/Rheumatology and Epidemiology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Psoriatic arthritis (PsA) is a heterogeneous chronic inflammatory disease that affects the skin, joints, and soft tissues. No metrics exist to indicate whether an…
  • Abstract Number: 2447 • 2018 ACR/ARHP Annual Meeting

    Liver Enzyme Abnormalities after Tofacitinib Treatment in Patients with Hepatic Steatosis from the Rheumatoid Arthritis, Psoriatic Arthritis, and Psoriasis Clinical Programs

    Enrique R Soriano1, Hugo Madariaga2, Oswaldo Castañeda3, Gustavo Citera4, Emilce E Schneeberger4, Mario H Cardiel5, Thijs Hendrikx6, Daniela Graham7, Harry Shi6 and Dario Ponce de Leon8, 1Hospital Italiano de Buenos Aires, Buenos Aires, Argentina, 2Clínica del Sur, Arequipa, Peru, 3Clínica Anglo Americana, Lima, Peru, 4Instituto de Rehabilitación Psicofísica, Buenos Aires, Argentina, 5Centro de Investigación Clínica de Morelia, Morelia, Mexico, 6Pfizer Inc, Collegeville, PA, 7Pfizer Inc, Groton, CT, 8Pfizer Inc, Lima, Peru

    Background/Purpose: Non-alcoholic fatty liver disease, characterized by hepatic steatosis (HS), is a very common form of chronic liver disease in many countries. Limited data are…
  • Abstract Number: 685 • 2018 ACR/ARHP Annual Meeting

    Changes in Key Laboratory Values with Tofacitinib 5mg BID Treatment in Patients with Psoriatic Arthritis and Rheumatoid Arthritis

    William FC Rigby1, Gerd R. Burmester2, Oliver FitzGerald3, Valderilio F Azevedo4, Peter Nash5, Thijs Hendrikx6, Daniela Graham7, Cunshan Wang7 and Thomas Jones6, 1Geisel School of Medicine at Dartmouth, Lebanon, NH, 2Charité – University Medicine Berlin, Berlin, Germany, 3Department of Rheumatology, St Vincent’s University Hospital, and Conway Institute for Biomolecular Research, University College, Dublin, Ireland, 4Universidade Federal do Paraná, Curitiba, Brazil, 5University of Queensland, Brisbane, Australia, 6Pfizer Inc, Collegeville, PA, 7Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of psoriatic arthritis (PsA) and rheumatoid arthritis (RA). In most countries where tofacitinib is…
  • Abstract Number: 2568 • 2018 ACR/ARHP Annual Meeting

    Secukinumab Provides Sustained Improvements in the Signs and Symptoms in Psoriatic Arthritis: Final 5 Year Efficacy and Safety Results from a Phase 3 Trial

    Philip J. Mease1, Arthur Kavanaugh2, Andreas Reimold3, Hasan Tahir4, Juergen Rech5, Stephen Hall6, Piet Geusens7, Pellet Pascale8, Evie Maria Delicha9, Luminita Pricop10 and Shephard Mpofu9, 1Swedish Medical Center and University of Washington School of Medicine, Seattle, WA, 2University of California, San Diego, School of Medicine, La Jolla, CA, 3Hospital of Southern Norway, Kristiansand, Norway, 4Rheumatology, Barts Health NHS Trust, London, United Kingdom, 5Universitätsklinikum Erlangen, Erlangen, Germany, 6Monash University,, Melbourne, Australia, 7University of Hasselt, Belgium and Maastricht University Hospital, Maastricht, Netherlands, 8Novartis Pharma AG, basel, Switzerland, 9Novartis Pharma AG, Basel, Switzerland, 10Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA, East Hanover, NJ

    Background/Purpose: Secukinumab (SEC), a fully human monoclonal IgG1 antibody, provided rapid and significant improvements in all key clinical domains of psoriatic arthritis (PsA) in the…
  • Abstract Number: 698 • 2018 ACR/ARHP Annual Meeting

    Discontinuation of Methotrexate or TNF Inhibitors in Patients with Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis

    Michael D. George1, Joshua Baker2 and Alexis Ogdie3, 1Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Philadelphia VA Medical Center and University of Pennsylvania, Philadelphia, PA, 3Medicine/Rheumatology and Epidemiology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Methotrexate and TNF inhibitors (TNFi) are commonly used in the treatment of RA, PsA, and other SpA. While MTX is a mainstay of RA…
  • Abstract Number: 2577 • 2018 ACR/ARHP Annual Meeting

    Long-Term Effect of Ixekizumab on Patient-Reported Outcomes in Patients with Psa and Inadequate Response to TNF Inhibitors: 2-Year Follow-up from a Phase 3 Study

    Anthony Turkiewicz1, Amanda M. Gellett2, Lisa Kerr2, Julie Birt2 and Jordi Gratacos3, 1Rheumatology Associates, Birmingham, AL, 2Eli Lilly and Company, Indianapolis, IN, 3Rheumatology, Hospital Parc Taulí, Sabadell - Barcelona, Spain

    Background/Purpose: PsA is a chronic and complex inflammatory disease with both articular and extra-articular symptoms, including joint pain, enthesitis, dactylitis, fatigue, and skin and nail…
  • Abstract Number: 702 • 2018 ACR/ARHP Annual Meeting

    Effect of Biologics on Radiographic Progression of Peripheral Joints in Patients with Psoriatic Arthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

    Dongze Wu1, Priscilla Wong1, James F Griffith2, Jiang Yue1 and Lai-Shan Tam3, 1Department of Medicine & Therapeutics, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China, Hong Kong, China, 2Department of Imaging and Interventional Radiology, The Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, China, 3Department of Medicine & Therapeutics, The Chinese University of Hong Kong, Hong Kong, Hong Kong

    Background/Purpose: Psoriatic arthritis (PsA) often leads to structural damage with resultant disability and reduced quality of life. Biologic disease modifying anti-rheumatic drugs (bDMARDs), including tumor…
  • Abstract Number: 2588 • 2018 ACR/ARHP Annual Meeting

    Baseline Pain Severity As a Predictor of Pain Improvement Following Treatment with Tofacitinib in Psoriatic Arthritis

    Alexis Ogdie1, Kurt de Vlam2, Andrew G Bushmakin3, Joseph C Cappelleri3, Philip J. Mease4, Roy Fleischmann5, Peter C. Taylor6, Valderilio F Azevedo7, Lara Fallon8, Anna Maniccia9 and John Woolcott10, 1University of Pennsylvania, Philadelphia, PA, 2UZ Leuven, Leuven, Belgium, 3Pfizer Inc, Groton, CT, 4Swedish Medical Center and University of Washington, Seattle, WA, 5University of Texas Southwestern Medical Center, Dallas, TX, 6University of Oxford, Oxford, United Kingdom, 7Universidade Federal do Paraná, Curitiba, Brazil, 8Pfizer Canada, Montreal, QC, Canada, 9Pfizer Inc, New York, NY, 10Pfizer Inc, Collegeville, PA

    Background/Purpose: Pain is a core domain of psoriatic arthritis (PsA), and it is recommended that all randomized controlled trials (RCTs) in patients (pts) with PsA…
  • Abstract Number: 1018 • 2018 ACR/ARHP Annual Meeting

    Tofacitinib Impairs Monocyte-Derived Dendritic Cell Differentiation in Rheumatoid Arthritis and Psoriatic Arthritis.

    Viviana Marzaioli1, Mary Canavan1, Achilleas Floudas1, Siobhan C. Wade1, Candice Low2, Douglas J. Veale2 and Ursula Fearon1, 1Molecular Rheumatology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland, 2Centre for Arthritis and Rheumatic Diseases, Dublin Academic Medical Centre, University College Dublin, Dublin, Ireland

    Background/Purpose: Tofacinitib (Pfizer) is an oral Janus kinase inhibitor, recently approved for the treatment of rheumatoid arthritis (RA) and psoriatic arthritis (PsA). Although its mechanism…
  • Abstract Number: 2594 • 2018 ACR/ARHP Annual Meeting

    Median Time to Pain Improvement in Patients with Psoriatic Arthritis Treated with Tofacitinib

    Kurt de Vlam1, Alexis Ogdie2, Andrew G Bushmakin3, Joseph C Cappelleri3, Roy Fleischmann4, Peter C. Taylor5, Valderilio F Azevedo6, Lara Fallon7, Anna Maniccia8, John Woolcott9 and Philip J. Mease10, 1UZ Leuven, Leuven, Belgium, 2University of Pennsylvania, Philadelphia, PA, 3Pfizer Inc, Groton, CT, 4University of Texas Southwestern Medical Center, Dallas, TX, 5University of Oxford, Oxford, United Kingdom, 6Universidade Federal do Paraná, Curitiba, Brazil, 7Pfizer Canada, Montreal, QC, Canada, 8Pfizer Inc, New York, NY, 9Pfizer Inc, Collegeville, PA, 10Swedish Medical Center and University of Washington, Seattle, WA

    Background/Purpose: Pain is a core domain of psoriatic arthritis (PsA).1 Rapid, sustained pain reduction is a priority for patients (pts) and physicians when choosing treatment.…
  • Abstract Number: 1224 • 2018 ACR/ARHP Annual Meeting

    High Rates of Conversion and Reversion of Tuberculosis Screening Assays in Rheumatic Patients during Long Term Biologic Treatment

    Konstantinos Thomas1, Anastasia Makris1, Christina Tsalapaki1, Argyro Lazarini1, Kalliopi Klavdianou1, Katerina Antonatou1, Christos Koutsianas1, Chrisoula Hatzara1, Emilia Hadziyannis1 and Dimitrios Vassilopoulos2, 1Clinical Immunology-Rheumatology Unit, 2nd Department of Medicine and Laboratory, Hippokration General Hospital, Joint Rheumatology Program, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece, 2Clinical Immunology-Rheumatology Unit, 2nd Department of Medicine and Laboratory, Hippokration General HospitalMedicine, Joint Rheumatology Program, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece

    Background/Purpose: Baseline screening for tuberculosis (TB) with tuberculin skin testing (TST) and/or interferon-gamma release assays (IGRAs) is recommended for all rheumatic patients starting biologic DMARDs…
  • Abstract Number: 2595 • 2018 ACR/ARHP Annual Meeting

    Golimumab Improves Socio- and Health Economic Parameters in Patients with RA, Psa and As: Real World-Data from a Non-Interventional Clinical Study in Germany

    Klaus Krüger1, Gerd R. Burmester2, Siegfried Wassenberg3, Valeria Biermann4 and Matthias H. Thomas5, 1Medical Centre of Rheumatology, Munich, Germany, 2Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany, 3Rheumazentrum Ratingen, Ratingen, Germany, 4Lehrstuhl für Gesundheitsmanagement, Universität Erlangen-Nürnberg, Nürnberg, Germany, 5Medical Affairs, MSD Sharp & Dohme GmbH, Haar, Germany

    Background/Purpose: Golimumab (GLM) has shown its efficacy and safety in various clinical trials. Data from socio- and health economic parameters and costs in daily clinical…
  • Abstract Number: 1517 • 2018 ACR/ARHP Annual Meeting

    Integrated Safety Analysis across Phase 3 Clinical Studies Including the Controlled and Uncontrolled Periods for Intravenous Golimumab in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis

    Arthur Kavanaugh1, Atul A. Deodhar2, Sergio Schwartzman3, Shelly Kafka4, Soumya D Chakravarty5, Elizabeth C Hsia6, Diane D. Harrison7, Jocelyn Leu7, Yiying Zhou7, Kim Hung Lo7 and M. Elaine Husni8, 1University of California, San Diego, School of Medicine, La Jolla, CA, 2Oregon Health & Science U, Portland, OR, 3Weill Cornell Medical College, New York, NY, 4Janssen Scientific Affairs, LLC, Horsham, PA, 5Janssen Scientific Affairs, LLC/Drexel University School of Medicine, Horsham/Phila, PA, 6Janssen Reseach & Development, LLC/ U of Pennsylvania School of Medicine, Spring House/Philadelphia, PA, 7Janssen Research & Development, LLC, Spring House, PA, 8Orthopedic and Rheumatologic Institute, Cleveland Clinic, Cleveland, OH

    Background/Purpose: The GO-FURTHER, GO-VIBRANT, and GO-ALIVE randomized controlled trials evaluated the efficacy and safety of intravenous (IV) golimumab (GLM) in patients (pts) with active rheumatoid…
  • Abstract Number: 2613 • 2018 ACR/ARHP Annual Meeting

    Patterns of Medication Use in a Validated Cohort of Psoriatic Arthritis (PsA) Patients

    Madeline J. Epsten1, Lisa A. Mandl1, Jackie Szymonifka2 and Sergio Schwartzman1, 1Rheumatology, Hospital for Special Surgery, New York, NY, 2Hospital for Special Surgery, New York, NY

    Background/Purpose:  There is currently a lack of consensus among experts on the optimal therapeutic management of psoriatic arthritis (PsA). EULAR and GRAPPA recommendations support initial…
  • Abstract Number: 1591 • 2018 ACR/ARHP Annual Meeting

    Is Enthesitis a Marker of Disease Severity in Early Psoriatic Arthritis?

    Lihi Eder1, Chandra Farrer2 and Dana Jerome3, 1Women's College Research Institute, University of Toronto, Women's College Hospital, Toronto, ON, Canada, 2Rheumatology, Women's College Hospital, Toronto, ON, Canada, 3University of Toronto, Women's College Hospital, Toronto, ON, Canada

    Background/Purpose: Enthesitis is a key feature in psoriatic arthritis (PsA) affecting approximately a third of the patients. Ultrasound improves the detection of enthesitis compared to…
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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 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.).

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