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Abstracts tagged "Disease-Modifying Antirheumatic Drugs (Dmards)"

  • Abstract Number: 0973 • ACR Convergence 2020

    Novel Network Tool Highlights Key Features Associated with Disease Pathotypes and Response to Treatment in Early Rheumatoid Arthritis

    Elisabetta Sciacca1, Anna Surace2, Myles Lewis1, Salvatore Alaimo3, Vito Latora4, Felice Rivellese1, Alfredo Pulvirenti3, Alfredo Ferro3 and Costantino Pitzalis5, 1Centre for Experimental Medicine and Rheumatology, Queen Mary University of London, London, United Kingdom, 2Centre for Experimental Medicine and Rheumatology, Queen Mary University of London, Liverpool, United Kingdom, 3Bioinformatics Unit, Dept of Clinical and Experimental Medicine, University of Catania, Catania, Sicilia, Italy, 4School of Mathematical Sciences Queen Mary, University of London, London, United Kingdom, 5Queen Mary University of London, London, United Kingdom

    Background/Purpose: Biomedical research uses many statistical/bioinformatics tools to find genes or proteins differentially expressed between patient group of interest. However, biological elements are related to…
  • Abstract Number: 1225 • ACR Convergence 2020

    Targeting to IL-6 or Specific JAKs for RA Treatment: Seeking a Rationale for Switching Each Other If One of These Treatments Resulted in Lack of Efficacy

    Yoshinobu Koyama1, Yoshiharu Sato2, Hiroshi Iijima2, Moe Sakamoto3 and Toshie Higuchi3, 1Okayama Red Cross Hospital, Japanese Red Cross Society, Okayama, Japan, 2DNA Chip Research Inc, Tokyo, Japan, 3Division of Rheumatology, Okayama Red Cross Hospital, Japanese Red Cross Society, Okayama, Japan

    Background/Purpose: Inhibition of IL-6 signaling is one of the most established strategies for RA treatment. Tocilizumab (TCZ) is the pioneer which blocks IL-6 signaling by…
  • Abstract Number: 1717 • ACR Convergence 2020

    Impact of Treatments on Favorable Outcome over the First 10 Years of Disease in Early Rheumatoid Arthritis: Results from a WCE Model in the ESPOIR Cohort

    Joanna Kedra1, David Hajage1, Alexandre Lafourcade1, Bernard Combe2, Maxime Dougados3 and Bruno Fautrel4, 1Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique, UMR S1136, Paris, France, Paris, France, 2University of Montpellier, Montpellier, France, 3Department of Rheumatology, Hopital Cochin, Université de Paris, Paris, France, 4Sorbonne University, INSERM, IPLES; Pitié-Salpêtrière Hospital, Paris, Ile-de-France, France

    Background/Purpose: Long-term observational studies on the prediction of favorable outcome (FO) in rheumatoid arthritis (RA) have mostly considered patients baseline characteristics and have rarely evaluated…
  • Abstract Number: 2000 • ACR Convergence 2020

    Risk of Venous Thromboembolism in Rheumatoid Arthritis Patients Treated with Methotrexate versus Hydroxychloroquine

    Mengdong He1, Ajinkya Pawar1, Rishi Desai1, Robert Glynn1, Hemin Lee1, Michael Weinblatt1, Daniel H Solomon1 and Seoyoung Kim1, 1Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Prior studies suggest an increased risk of venous thromboembolism (VTE) among patients with rheumatoid arthritis (RA). However, little is known about the comparative risk…
  • Abstract Number: 0211 • ACR Convergence 2020

    Efficacy and Safety of Upadacitinib in Patients from China, Brazil, and South Korea with Rheumatoid Arthritis Who Have Had Inadequate Response to Conventional Synthetic Disease-modifying Antirheumatic Drugs

    Xiaofeng Zeng1, Dongbao Zhao2, Sebastiao Radominski3, Mauro Keiserman4, Chang Keun Lee5, Sebastian Meerwein6, Jeffrey Enejosa7, Yunxia Sui7, Mohamed-Eslam Mohamed7 and Won Park8, 1Department of Rheumatology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Beijing, China (People's Republic), 2Shanghai Changhai Hospital, Shanghai, China (People's Republic), 3Universidade Federal do Paraná, Curitiba, Brazil, 4Pontificial Catholic University, Porto Alegre, Brazil, 5Asan Medical Center, Seoul, Republic of Korea, 6Pharmaceutical Development, AbbVie Deutschland GmbH & Co KG, Ludwigshafen, Germany, 7AbbVie Inc., North Chicago, IL, 8Inha University, Incheon, Republic of Korea

    Background/Purpose: This Phase 3, randomized, double-blind, placebo (PBO)-controlled study assessed the efficacy and safety of upadacitinib (UPA) in combination with csDMARDs in patients with rheumatoid…
  • Abstract Number: 0450 • ACR Convergence 2020

    In Vitro Characterization of Inflammatory Arthritis Associated with Immune Check Point Inhibition

    Anne Sofie Sørensen1, Morten Nørgaard Andersen1, Kristian Juul-Madsen2, Cæcilie Deisting Skejø1, Henrik Schmidt1, Thomas Vorup-Jensen1 and Tue Wenzel Kragstrup1, 1Aarhus University, Aarhus, Denmark, 2Aarhus University, Aarhus, Midtjylland, Denmark

    Background/Purpose: During treatment with immune checkpoint inhibitors (ICI) such as the anti-PD-1 antibody pembrolizumab, 2-4% of cancer patients develop inflammatory arthritis as an immune-related adverse…
  • Abstract Number: 0803 • ACR Convergence 2020

    Real-World DMARD Experience and Outcomes for Rheumatoid Arthritis Patients in Japan: Safety

    Mitsumasa Kishimoto1, Yoshiya Tanaka2, Leslie Harrold3, Alina Onofrei3, Christine Barr4, Ekta Agarwal5, Jose L Rivas6, Naonobu Sugiyama7, Jeffrey Greenberg8 and Hisashi Yamanaka9, 1Department of Nephrology and Rheumatology, Kyorin University School of Medicine, Yokohama, Japan, 2The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 3Corrona, LLC, Waltham, MA, 4Corrona, LLC, Albany, NY, 5Pfizer, Inc., Princeton Jct, NJ, 6Pfizer SLU, Madrid, Spain, 7Pfizer Japan Inc, Tokyo, Japan, 8Corrona, LLC and NYU School of Medicine, Waltham, MA, 9Sanno Medical Center, Tokyo, Japan, Tokyo, Japan

    Background/Purpose: There is limited information on the real-world safety of disease-modifying anti-rheumatic drugs (DMARDs) approved for treating rheumatoid arthritis (RA) in Japan. Using a Japanese…
  • Abstract Number: 0983 • ACR Convergence 2020

    Outcomes Following Antimalarial Withdrawal in Patients with Quiescent Systemic Lupus Erythematosus

    Danae Papachristos1, Dafna Gladman2, Jiandong Su3 and Murray Urowitz4, 1University Health Network, Toronto, ON, Canada, 2Krembil Research Institute, Toronto Western Hospital, Toronto, ON, Canada, 3University of Toronto Lupus Clinic, Centre for Prognosis Studies in Rheumatic Diseases, Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 4University Health Network, University of Toronto, Toronto, ON, Canada

    Background/Purpose: Antimalarial medications (AMs) are central to the management of SLE, affording numerous clinical benefits including the reduction of disease flare. However, little is known…
  • Abstract Number: 1228 • ACR Convergence 2020

    Baricitinib 2-mg Provides Greater Improvements in Patient-Reported Outcomes Across All Disease Activity Levels Compared to Placebo: Post-hoc Analyses of RA-BEACON and RA-BUILD Trials

    Clifton Bingham III1, Bochao Jia2, Jianmin Wu2, Amanda Quebe2, Carol Kannowski2, Susan Otawa2, Yun-Fei Chen2, Kirstin Griffing2, Dongyi He3 and Dalton Sholter4, 1Johns Hopkins University, Baltimore, MD, 2Eli Lilly and Company, Indianapolis, IN, 3Shanghai Guanghua Hospital, Shanghai, Shanghai, China (People's Republic), 4University of Alberta, Edmonton, AB, Canada

    Background/Purpose: Baricitinib (BARI) improved patient-reported outcomes (PROs) in patients with insufficient response or intolerance to ≥1 tumor necrosis factor inhibitors (TNFi) or other biological disease-modifying…
  • Abstract Number: 1718 • ACR Convergence 2020

    Impact of Treatments on Radiographic Progression over the First 10 Years of Disease in Early Rheumatoid Arthritis: Results from the ESPOIR Cohort

    Joanna Kedra1, David Hajage1, Alexandre Lafourcade1, Bernard Combe2, Maxime Dougados3 and Bruno Fautrel4, 1Sorbonne Université, Institut Pierre Louis d'Epidémiologie et de Santé Publique, UMR S1136, Paris, France, Paris, France, 2University of Montpellier, Montpellier, France, 3Department of Rheumatology, Hopital Cochin, Université de Paris, Paris, France, 4Sorbonne University, INSERM, IPLES; Pitié-Salpêtrière Hospital, Paris, Ile-de-France, France

    Background/Purpose: Long-term observational studies on the prediction of structural damage progression (SDP) in rheumatoid arthritis (RA) have mostly considered patients baseline characteristics and have rarely…
  • Abstract Number: 2001 • ACR Convergence 2020

    Adverse Effects of Low Dose Methotrexate: Adjudicated Hematologic Outcomes in a Large Randomized Double-blind Placebo-controlled Trial

    Kathleen Vanni1, Nancy Berliner1, Nina Paynter2, Robert Glynn2, Jean MacFadyen1, Joshua Colls1, Fengxin Lu1, Chang Xu2, Paul Ridker1 and Daniel H Solomon1, 1Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston

    Background/Purpose: Low dose methotrexate (LD-MTX), a cornerstone in the treatment of rheumatoid arthritis, is associated with a moderately increased risk of anemia and leukopenia, but…
  • Abstract Number: 0213 • ACR Convergence 2020

    Sustainability of Response to Upadacitinib as Monotherapy or in Combination Among Patients with Rheumatoid Arthritis and Prior Inadequate Response to Conventional Synthetic DMARDs

    Arthur Kavanaugh1, Maya Buch2, Bernard Combe3, Louis Bessette4, In-Ho Song5, Yanna Song6, Jessica Suboticki5 and Peter Nash7, 1Division of Rheumatology, Allergy, & Immunology, University of California San Diego Medical School, San Diego, CA, 2Centre of Musculoskeletal Research, School of Biological Sciences, University of Manchester, Manchester, United Kingdom, 3University of Montpellier, Montpellier, France, 4Laval University, Quebec, Canada, 5AbbVie Inc., North Chicago, IL, 6AbbVie Inc., North Chicago,, IL, 7School of Medicine Griffith University, Brisbane, Queensland, Australia

    Background/Purpose: To assess long-term sustainability of responses to upadacitinib (UPA), a JAK inhibitor, with or without background csDMARD(s) in patients (pts) with rheumatoid arthritis (RA).Methods:…
  • Abstract Number: 0466 • ACR Convergence 2020

    Dosage Modification of Immunomodulatory Medications by Rheumatology Patients in New York City During the Peak of the COVID-19 Pandemic

    Marianna Frey1, Gregory Vitone2, Candace Feldman3, Lindsay Lally1, Anne Bass4, Jane Salmon1, Mary Crow1, Michael Lockshin5, Vivian Bykerk1, Lisa Mandl1 and Medha Barbhaiya5, 1Hospital for Special Surgery, New York, NY, 2Hospital for Special Surgery, New York, 3Brigham and Women's Hospital, Boston, 4Hospital for Special Surgery/Weill Cornell Medicine, New York, NY, 5Hospital for Special Surgery, Barbara Volcker Center for Women and Rheumatic Diseases, New York, NY

    Background/Purpose: Due to concerns about underlying immune dysregulation and immunosuppression, patients with systemic rheumatic diseases living in COVID-19 “hot spots” may have modified their immunomodulatory…
  • Abstract Number: 0806 • ACR Convergence 2020

    Identification and Adjustment for Factors Associated with Clinical Response in Rheumatoid Arthritis Clinical Trials to Improve Comparisons of Treatment Efficacy

    Anthony Cordisco1 and Joshua Baker1, 1Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Numerous clinical trials have been published in rheumatoid arthritis (RA), but comparing efficacies of disease-modifying anti-rheumatic drugs (DMARDs) is complicated by a lack of…
  • Abstract Number: 1001 • ACR Convergence 2020

    Risk of Malignant Melanoma and Nonmelanoma Skin Cancer in Rheumatoid Arthritis Patients Initiating Methotrexate versus Hydroxychloroquine

    Hemin Lee1, Sarah Chen2, Nileesa Gautam2, Seanna Vine1, Mengdong He2, Rishi Desai2, Michael Weinblatt1, Robert Glynn2 and Seoyoung Kim2, 1Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston

    Background/Purpose: Previous randomized clinical trials and observational studies have signaled an increased risk of skin cancer in rheumatoid arthritis (RA) patients treated with immunosuppressants such…
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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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