ACR Meeting Abstracts

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  • Abstract Number: 2044 • 2015 ACR/ARHP Annual Meeting

    Axonal Dysfunction in Childhood-Onset Systemic Lupus Erythematosus. Association with Neuropsychiatric Manifestations and Disease Activity

    Renan Frittoli1, Mariana Postal2, Karina Pelicari2, Nailu Sinicato3, Aline Tamires Lapa4, Fernando Peres1, Fernando Cendes5, Roberto Marini Sr.6, Gabriela Castellano7, Leticia Rittner8 and Simone Appenzeller2, 1State University of Campinas, Campinas, Brazil, 2Medicine, State University of Campinas, Campinas, Brazil, 3pEDIATRICS, State University of Campinas, Campinas, Brazil, 4Rua Alexandre Fleming, Fcm09-Baraogeraldo, Campinas, Brazil, 5Neurology, State University of Campinas, Campinas, Brazil, 6Pediatric Rheumatology Unit, State University of Campinas, São Paulo, Brazil, 7Medical Physics, State University of Campinas, Campinas, Brazil, 8Electrical Engineering, State University of Campinas, Campinas, Brazil

    Background/Purpose: Involvement of the central nervous system is frequently observed in childhood-onset SLE patients (cSLE). Proton magnetic spectroscopy (1H-MRS) is an important non-invasive method of…
  • Abstract Number: 2045 • 2015 ACR/ARHP Annual Meeting

    Cross-Validation of the Pediatric Automated Neuropsychological Assessment Metrics-Cognitive Performance Scores in the Screening of Neurocognitive Impairment in Childhood-Onset Systemic Lupus Erythematosus

    Jasmine Nguyen1, Tricia Williams2, Earl Silverman3 and Deborah M. Levy4, 1Royal College of Surgeons in Ireland, Dublin, Ireland, 2Psychology, Hospital for Sick Children, Toronto, ON, Canada, 3Division of Rheumatology, Hospital for Sick Children and University of Toronto, Toronto, ON, Canada, 4Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada

    Background/Purpose: Neurocognitive impairment (NCI) is an important morbidity in childhood-onset systemic lupus erythematosus (cSLE); however, the gold standard formal neuropsychological assessment is difficult to access. Screening for…
  • Abstract Number: 2046 • 2015 ACR/ARHP Annual Meeting

    Long-Term Outcomes in Cardiac Neonatal Lupus and Associated Risk Factors for Morbidity

    Amit Saxena1, Peter M. Izmirly1, Sara Sahl1, Deborah Friedman2 and Jill P. Buyon3, 1Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY, 2Pediatric Cardiology, New York Medical College, Valhalla, NY, 3Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: All women with anti-Ro antibodies face the risk of cardiac neonatal lupus (cardiac NL), which presents as congenital heart block (CHB) and/or cardiomyopathy in…
  • Abstract Number: 2047 • 2015 ACR/ARHP Annual Meeting

    A Randomised Double-Blind Placebo-Controlled Trial of Vitamin D Supplementation in Juvenile-Onset Systemic Lupus Erythematosus: Effects on Microarchitecture Measured By HR-pQCT

    Glauce Lima1, Juliane Paupitz1, Nadia E Aikawa2, Jackeline Couto Alvarenga3, Eloisa Bonfá1 and Rosa M R Pereira4, 1Rheumatology Division, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 2Rheumatology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 3Division of Rheumatology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 4Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil

    Background/Purpose: Vitamin D has an important effect in bone quality and vitamin D deficiency in Juvenile-onset Systemic Lupus Erythematosus patients (JoSLE) may be associated with…
  • Abstract Number: 2048 • 2015 ACR/ARHP Annual Meeting

    Hospitalization Trends of Rheumatoid Arthritis and Gout in the United States: A Crossroad

    Sian Yik Lim1, Na Lu1, Mark Fisher1, Amar Oza1, Sharan K. Rai2, Mariano E Menendez1 and Hyon Choi1, 1Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, 2Experimental Medicine, University of British Columbia, Vancouver, BC, Canada

    Background/Purpose:  Rheumatoid arthritis (RA) and gout are the two most common inflammatory arthritides in the US and beyond. As hospitalization for these conditions are known…
  • Abstract Number: 2049 • 2015 ACR/ARHP Annual Meeting

    Long Term Effectiveness of Herpes Zoster Vaccine Among Patients with Autoimmune and Inflammatory Diseases

    Huifeng Yun1, Fenglong Xie2, John Baddley3, Kevin L. Winthrop4, Lang Chen5 and Jeffrey R. Curtis6, 1Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 2Rheumatology & Immunology, University of Alabama at Birmingham, Birmingham, AL, 3Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Oregon Health and Science University, Portland, OR, 5University of Alabama at Bimingham, Birmingham, AL, 6University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: The live herpes zoster (HZ) vaccine is effective in healthy older people to reduce the incidence and burden of HZ.  Recent results from a…
  • Abstract Number: 2050 • 2015 ACR/ARHP Annual Meeting

    Herpes Zoster during the Tofacitinib Clinical Development Program for RA: Characterization of Herpes Zoster Incidence and Evaluation of Whether Herpes Zoster Predicts Subsequent Serious Infections or Malignancy

    Kevin L. Winthrop1, Yoshiya Tanaka2, Kunihiro Yamaoka3, Jeffrey R. Curtis4, Chudy Nduaka5, Haiyun Fan5, Pinaki Biswas6, Tomohiro Hirose7, Sriram Krishnaswami8, Hernan Valdez6, Shigeyuki Toyoizumi7, Koshika Soma8 and Connie Chen6, 1Oregon Health & Science University, Portland, OR, 2The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 3Keio University, Tokyo, Japan, 4University of Alabama at Birmingham, Birmingham, AL, 5Pfizer Inc, Collegeville, PA, 6Pfizer Inc, New York, NY, 7Pfizer Japan Inc, Tokyo, Japan, 8Pfizer Inc, Groton, CT

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of RA. The risk of herpes zoster (HZ) was elevated within the tofacitinib clinical…
  • Abstract Number: 2051 • 2015 ACR/ARHP Annual Meeting

    Risk for Lower Intestinal Perforations in RA Patients Treated with Tocilizumab in Comparison to Treatment with TNF Inhibitors, Rituximab, Abatacept or Conventional Synthetic Dmards

    Anja Strangfeld1, Adrian Richter2, Peter Herzer3, Karin Rockwitz4, Winfried Demary5, Martin Aringer6, Angela Zink7 and Joachim Listing8, 1Epidemiology, German Rheumatism Research Center, Berlin, Germany, 2German Rheumatism Research Center, Berlin, Germany, 3Rheumatologist, Scientific Advisory Board, München, Germany, 4Rheumatologic Practice, Goslar, Germany, 5Rheumatologist, Hildesheim, Germany, 6Rheumatology, Medicine III, University Clinical Center, Technical University Dresden, Dresden, Germany, 7Epidemiologie, Deutsches Rheuma-Forschungszentrum, Berlin, Germany, 8Epidemiology, DRFZ, Berlin, Germany

    Background/Purpose: Interleukin-6 has a direct protective effect on intestinal cells. Although several cases of lower intestinal perforations (LIP) were reported in clinical trials of tocilizumab…
  • Abstract Number: 2052 • 2015 ACR/ARHP Annual Meeting

    Lymphoma in Patients with Rheumatoid Arthritis Treated with Biologic Drugs:  Long-Term Follow-up of Risks and Lymphoma Subtypes

    Karin Hellgren1, Christer Sundström2, Johan Askling3, Eva Baecklund4 and on behalf of the ARTIS study group, 1Clinical Epidemiology Unit and Rheumatology Unit, Department of Medicine, Karolinska Institute at Karolinska University Hospital, Stockholm, Sweden, 2Department of Genetics and Pathology, Uppsala University, Uppsala, Sweden, 3Clinical Epidemiology Unit and Rheumatology Unit, Department of Medicine, Karolinska Institute, Stockholm, Sweden, 4Rheumatology, Department of Medical Sciences, University Hospital, Uppsala, Sweden

    Background/Purpose: The long-term lymphoma risk in patients with rheumatoid arthritis (RA) treated with biologic disease modifying anti-rheumatic drugs (bDMARDs) remains a concern. The aim of…
  • Abstract Number: 2053 • 2015 ACR/ARHP Annual Meeting

    Adjustment of Skeletal Muscle Mass Estimates for the Extent of Adiposity Strengthens Relationships with Functional Outcomes in Rheumatoid Arthritis

    Joshua Baker1, Jon Giles2, Mary Leonard3, David Weber4, Jin Long5, Erik Jorgenson6 and Patricia P. Katz7, 1Medicine/Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Rheumatology, Columbia University Medical Center, NY, NY, 3Stanford University, Palo Alto, CA, 4Rochester University, Rochester, NY, 5Children's Hospital of Philadelphia, Philadelphia, PA, 6University of Pennsylvania, Philadelphia, PA, 7Rheumatology, UCSF, SF, CA

    Background/Purpose: Skeletal muscle loss in rheumatoid arthritis (RA) has been described in association with poor physical functioning. Greater adiposity is simultaneously associated with both greater…
  • Abstract Number: 2054 • 2015 ACR/ARHP Annual Meeting

    Randomized, Double-Blind, Phase 3 Study of Efficacy and Safety of ABP 501 Compared with Adalimumab in Subjects with Moderate to Severe Rheumatoid Arthritis

    Stanley B. Cohen1, Mark C. Genovese2, Ernest H. Choy3, Fernando Perez-Ruiz4, Jose L. Pablos5, Nan Zhang6 and Primal Kaur7, 1Metroplex Clinical Research Center, Dallas, TX, 2Division of Rheumatology, Stanford University Medical Center, Palo Alto, CA, 3Cardiff University, Institute of Infection and Immunity, Tenovus Building, University Hospital of Wales, Cardiff, United Kingdom, 4Servicio de Reumatología, Vizcaya, Spain, 5Instituto de Investigacion Hospital, Madrid, Spain, 6Biosimilars, Amgen, Inc., Thousand Oaks, CA, 7Amgen, Inc., Thousand Oaks, CA

    Background/Purpose: ABP 501 is being developed as a biosimilar candidate to adalimumab (Humira®), a fully human recombinant monoclonal antibody. Evidence from analytical comparisons indicates that…
  • Abstract Number: 2055 • 2015 ACR/ARHP Annual Meeting

    A Phase III, Randomized, Double-Blind Clinical Study Comparing SB4, an Etanercept Biosimilar, with Etanercept Reference Product (Enbrel®) in Patients with Moderate to Severe Rheumatoid Arthritis Despite Methotrexate Therapy (52-week Results)

    Jiri Vencovsky1, Anna Sylwestrzak2, Piotr Leszczyñski3, Wieslawa Porawska4, Asta Baranauskaite5, Vira Tseluyko6, Vyacheslav Zhdan7, Barbara Stasiuk8, Roma Milasiene9, Aaron Alejandro Barrera Rodriguez10, Soo Yeon Cheong11, Jeehoon Ghil11 and Paul Emery12, 1Rheumatology, Institute of Rheumatology and Department of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 2NZOZ Medica Pro Familia Sp. z o.o., Warsaw, Poland, 3Rheumatology and Rehabilitation, Poznan University of Medical Sciences, Poznan, Poland, 4Poznanski Osrodek Medyczny NOVAMED, Poznan, Poland, 5Lithuanian University of Health Sciences, Kaunas, Lithuania, 6Internal Medicine and Rheumatology, Kharkiv Medical Academy of Postgraduate Education, Kharkiv, Ukraine, 7M.V.Sklifosovskyi Poltava Regional Clinical Hospital, Poltava, Ukraine, 8Medicome Sp. z o.o., Oswiecim, Poland, 9Klaipeda University Hospital, Klaipeda, Lithuania, 10Unidad de Atención Medica e Investigación en Salud (UNAMIS), Yucatán, Mexico, 11Samsung Bioepis Co., Ltd., Incheon, South Korea, 12Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom

    Background/Purpose: SB4 is a biologic agent developed as a biosimilar of the etanercept reference product (ETN). This study was a randomized, double-blind, multicenter study and…
  • Abstract Number: 2056 • 2015 ACR/ARHP Annual Meeting

    A Randomized, Double-Blind, Phase III Study Comparing SB2, an Infliximab Biosimilar, to the Infliximab Reference Product (Remicade®) in Patients with Moderate to Severe Rheumatoid Arthritis Despite Methotrexate Therapy: 54-Week Results

    Jung-Yoon Choe1, Nenad Prodanovic2, Jaroslaw Niebrzydowski3, Ivan Staykov4, Eva Dokoupilova5, Asta Baranauskaite6, Roman Yatsyshyn7, Mevludin Mekic8, Wieslawa Porawska9, Hana Ciferska10, Krystyna Jedrychowicz-Rosiak11, Agnieszka Zielinska12, Jasmine Choi13, Young Hee Rho13 and Josef S. Smolen14, 1Division of Rheumatology, Daegu Catholic University Medical Center, Daegu, South Korea, 2Clinical Center Banja Luka, Banja Luka, Bosnia, 3Medica Pro Familia, Gdynia, Poland, 4MHAT "Dr. Ivan Seliminski", AD, Sliven, Bulgaria, 5MEDICAL PLUS s.r.o, Uherske Hradiste, Czech Republic, 6Lithuanian University of Health Sciences, Kaunas, Lithuania, 7SHEI Ivano-Frankivsk NMU, Ivano-Frankivsk, Ukraine, 8University Clinic Centre Sarajevo, Sarajevo, Bosnia, 9Poznanski Osrodek Medyczny NOVAMED, Poznan, Poland, 10Revmatologicky ustav, Praha 2, Czech Republic, 11MCBK S.C., Grodzisk Mazowiecki, Poland, 12Medica Pro Familia Sp. z o.o. Spolka Komandytowo-Akcyjna, Warszawa, Poland, 13Samsung Bioepis Co., Ltd., Incheon, South Korea, 14Medical University of Vienna, Vienna, Austria

    Background/Purpose: SB2 is developed as a biosimilar of the infliximab reference product (INF). 30-week efficacy and safety results from a randomized phase III study were…
  • Abstract Number: 2057 • 2015 ACR/ARHP Annual Meeting

    Antibodies to Infliximab in Remicade-Treated Rheumatic Patients Show Identical Reactivity Towards Biosimilars

    Begoña Ruiz-Argüello1, Ainara Maguregui1, Ainhoa Ruiz del Agua1, Dora Pascual-Salcedo2, Ana Martínez2, Teresa Jurado3, Chamaida Plasencia4, Alejandro Balsa5, Francisca Llinares-Tello6, José Rosas7, Nerea Torres1, Antonio Martínez1 and Daniel Nagore1, 1R&D, Progenika-Grifols, Derio, Spain, 2Immunology Unit, La Paz University Hospital-Immunology, Madrid, Spain, 3Immunology, La Paz University Hospital-Idipaz, Madrid, Spain, 4Rheumatology Unit, La Paz University Hospital-Rheumatology, Madrid, Spain, 5Rheumatology, La Paz University Hospital-Rheumatology Department, Madrid, Spain, 6Clinical Analysis, Hospital Marina Baixa, Clinical Analysis, Villajoyosa, Spain, 7Rheumatology, Hospital Marina Baixa, Villajoyosa, Spain

    Background/Purpose: Infliximab (IFX) is the most immunogenic of anti-TNFα drugs available to treat patients with rheumatic diseases. The recent approval of the first infliximab biosimilars in…
  • Abstract Number: 2058 • 2015 ACR/ARHP Annual Meeting

    Efficacy and Safety of Rituximab Biosimilar Candidate (CT-P10) and Innovator Rituximab in Patients with Rheumatoid Arthritis: Results from Phase I Randomized Controlled Trial over 72 Weeks

    Dae-Hyun Yoo1, Won Park2, Chang-Hee Suh3, Seung-Cheol Shim4, Slawomir Jeka5, Fidencio Cons Molina6, Pawel Hrycaj7, Wolfgang Spieler8, Piotr Wiland9, Jan Brzezicki10, Eun Young Lee11, Francisco G. Medina-Rodriguez12, Pavel Shesternya13, Sebastiao Radominski14, Marina Stanislav15, Volodymyr Kovalenko16, Donghyuk Sheen17, Leysan Myasoutova18, Mie Jin Lim19, Jung-Yoon Choe20, Taek S. Kwon21 and Sang Joon Lee21, 1Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, South Korea, 2Division of Rheumatology, Department of Internal Medicine, Inha University Hospital, Incheon, South Korea, 3Department of Rheumatology, Ajou University Hospital, Suwon, South Korea, 4Department of Internal Medicine, Chungnam National University Hospital, Daejeon, South Korea, 5University Hospital Nr 2 Dr. Jan Biziel, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, Clinic of Rheumatology and Connective Tissue Diseases, Bydgoszcz, Poland, 6Centro de Investigacion en Artritis y Osteoporosis, Mexicali, Mexico, 7Department of Rheumatology and Clinical Immunology, Poznan University of Medical Sciences, Poznan, Poland, 8Osteologie und Rheumatologie, ZeFOR GmbH Zentrum für Forschung, Zerbst, Germany, 9Department of Rheumatology, Medical University of Wroclaw, Wroclaw, Poland, 10Wojewodzki Szpital Zespolony w Elablagu, Elblag, Poland, 11Division of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea, 12Rheumatology, LaSalle University, Mexico City, Mexico, 13Rheumatology Department, Krasnoyarsk State Medical University, Krasnoyarsk, Russia, 14CETI-Centro de estudos em Terapias Inovadoras, Universidade Federal do Parana, Curitiba, Brazil, 15Research Rheumatology Institute n. a. V.A. Nassonova, Moscow, Russia, 16Section of Non-coronarogenic Myocardial Diseases and Clinical Rheumatology, National Scientific Center, Kiev, Ukraine, 17Rheumatology, Eulji University Hospital, Daejeon, South Korea, 18City Reumatology Center, Research Medical Complex Vashe Zdorovie, Kazan, Russia, 19Division of Rheumatology, Departments of Internal Medicine, Inha University Hospital, Incheion, South Korea, 20Internal Medicine, Catholic University of Daegu, School of Medicine, Daegu, South Korea, 21CELLTRION, Inc., Incheon, South Korea

    Background/Purpose: CT-P10 is a biosimilar candidate of innovator rituximab (RTX). PK profile and clinical data up to week 24 has been reported at ACR 20131.…
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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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