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Abstracts tagged "methotrexate (MTX)"

  • Abstract Number: 609 • 2015 ACR/ARHP Annual Meeting

    A Reduction in Serum Uric Acid Levels May be Related to Methotrexate Efficacy in Early Rheumatoid Arthritis: Data from a Canadian Arthritis Cohort

    Jason Lee1, VP Bykerk2, George Dresser3, Gilles Boire4, Boulos Haraoui5, Carol Hitchon6, J Carter Thorne2, Diane Tin7, Shahin Jamal8, Edward C. Keystone9, Janet E. Pope10 and CATCH Investigators, 1Rheumatology, Western University, St. Joseph's Hospital, London, ON, Canada, 2University of Toronto, Toronto, ON, Canada, 3Clinical Pharmacology and Toxicology, Western University, London, ON, Canada, 4Department of Medicine/Division of Rheumatology, Université de Sherbrooke, Sherbrooke, QC, Canada, 5Institut de Rhumatologie, Montreal, QC, Canada, 6University of Manitoba, Winnipeg, MB, Canada, 7The Arthritis Program, Southlake Regional Health Centre, Newmarket, ON, Canada, 8Vancouver Coastal Health, Vancouver, BC, Canada, 9Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada, 10Monsignor Roney Bldg/Rheum, University of Western Ontario, St Joseph Health Care, London, ON, Canada

    Background/Purpose: The mechanism of methotrexate in rheumatoid arthritis (RA) is complex. It may increase adenosine levels by blocking conversion to of xanthine to uric acid…
  • Abstract Number: 3194 • 2015 ACR/ARHP Annual Meeting

    Oral to Subcutaneous Methotrexate Dose-Conversion Strategies in the Treatment of Rheumatoid Arthritis

    Michael Schiff1 and Peter Sadowski2, 1Division of Rheumatology, University of Colorado, Denver, CO, 2Antares Pharma Inc., Minneapolis, MN

    Background/Purpose: Methotrexate (MTX) is the cornerstone of rheumatoid arthritis (RA) therapy1 but absorption saturation limitations compromise oral MTX bioavailability (BA). Subcutaneous (SC) MTX has a…
  • Abstract Number: 1024 • 2015 ACR/ARHP Annual Meeting

    Disruptions in Folate Homeostasis May Lead to Increased Risk for Methotrexate Intolerance in Juvenile Idiopathic Arthritis

    Mara L Becker1, Leon van Haandel2, Ryan Funk3, Rodger Gaedigk4 and J.S. Leeder5, 1Rheumatology, Children's Mercy Kansas City, Kansas City, MO, 2Clinical Pharmacology, Medical Toxicology, and Therapeutic Innovation, Children's Mercy Kansas City, Kansas City, MO, 3University of Kansas Medical Center, Kansas City, KS, 4Clinical Pharmacology, medical Toxicology and Therapeutic Innovation, Children's Mercy Kansas City, Kansas City, MO, 5Clinical Pharmacology, Medical Toxicology and Therapeutic Innovation, Children's Mercy Kansas City, Kansas City, MO

    Background/Purpose: Despite widespread use, there remain no clear predictors of methotrexate (MTX) response or toxicity in Juvenile Idiopathic Arthritis (JIA).  With the utilization of new…
  • Abstract Number: 3197 • 2015 ACR/ARHP Annual Meeting

    Clinical Practice Experience in Rheumatoid Arthritis Patients Treated with Triple Therapy and Methotrexate-Tumor Necrosis Factor Inhibition Differs from That of Randomized Controlled Trials

    Daniel Erhardt1, Brian Sauer2, Chia-Chen Teng3, Ted R. Mikuls4, Jeffrey R. Curtis5, Derek Tang6, Bradley S. Stolshek6 and Grant W. Cannon1, 1Division of Rheumatology, Salt Lake City VA Medical Center and University of Utah, Salt Lake City, UT, 2Salt Lake City VA Medical Center and University of Utah, Salt Lake City, UT, 3HSR&D SLC VA Medical Center and University of Utah, Salt Lake City, UT, 4University of Nebraska Medical Center, Omaha, NE, 5University of Alabama at Birmingham, Birmingham, AL, 6Amgen, Inc., Thousand Oaks, CA

    Background/Purpose: Recently published randomized controlled trials (RCTs) have demonstrated similar outcomes in rheumatoid arthritis (RA) patients treated with triple therapy [methotrexate (MTX), sulfasalazine (SUL) and…
  • Abstract Number: 1039 • 2015 ACR/ARHP Annual Meeting

    The Safety and Effect on Disease Activity of Tocilizumab in Combination with MTX Versus Tocilizumab Monotherapy in Patients with Mild to Moderate RA: An Attempt to Optimise the Treatment Response

    Burkhard Leeb1,2, Raimund Lunzer3, Peter Fasching4, Manfred Herold5, O. Zamani6, Winfried Graninger7 and OPTIMISE trial Investigators, 12nd Dept. of Medicine, State Hospital Stockerau, Center for Rheumatology Lower Austria, Stockerau, Austria, 2Department of Clinical Rheumatology, Karl Landsteiner Society, Stockerau, Austria, 3Department of Internal Medicine, Hospital Barmherzige Brüder Graz-Eggenberg, Graz, Austria, 4Department of Internal Medicine V, Wilhelminen Hospital Vienna, Vienna, Austria, 5Internal Medicine VI, Medical University of Innsbruck, Austria, Innsbruck, Austria, 6Rheumazentrum Favoriten, Wien, Austria, 7Rheumatology and Immunology, Medical University of Graz, Graz, Austria

    Background/Purpose: An Austrian multi-center study of the effect on disease activity and the safety of Tocilizumab (TCZ) in combination with Methotrexate (MTX) versus TCZ Monotherapy…
  • Abstract Number: 3239 • 2015 ACR/ARHP Annual Meeting

    Response to Methotrexate Predicts Mortality in Rheumatoid Arthritis up to 30 Years

    Carolin Krause1, Siegfried Wassenberg2, Rolf Rau3, Gertraud Herborn4, Juergen Braun5 and Dietmar Krause6, 1University Munster, Munster, Germany, 2Rheumaklinik, Themistocles Gluck hospital - Rheumazentrum Ratingen, Ratingen, Germany, 3Expert in Rheumatology, Düsseldorf, Germany, 4Evangelisches Fachkrankenhaus Ratingen, Ratingen, Greece, 5Rheumazentrum Ruhrgebiet, Herne, Germany, 6Dept. for Medical Informatics, Biometry and Epidemiology, Ruhr University, Bochum, Germany

    Background/Purpose: Methotrexate (MTX) is considered as the anchor drug for the treatment of patients with rheumatoid arthritis (RA). MTX has been shown to reduce disease…
  • Abstract Number: 1041 • 2015 ACR/ARHP Annual Meeting

    Methotrexate Monotherapy and Methotrexate Combination Therapy with Traditional and Biologic Dmards for Rheumatoid Arthritis: A Cochrane Systematic Review and Network Meta-Analysis

    Glen S. Hazlewood1,2, Cheryl Barnabe3, George A. Tomlinson4, Deborah Marshall5, Daniel Devoe5 and Claire Bombardier6, 1Institute of Health, Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 2Medicine, University of Calgary, Calgary, AB, Canada, 3Cumming School of Medicine, University of Calgary, Calgary, AB, Canada, 4Institute for Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 5University of Calgary, Calgary, AB, Canada, 618 Strathearn Blvd, University of Toronto, Toronto, ON, Canada

    Background/Purpose: To compare methotrexate based disease-modifying anti-rheumatic drug (DMARD) treatments for rheumatoid arthritis in patients naïve to or after an inadequate response (IR) to methotrexate.  …
  • Abstract Number: 3247 • 2015 ACR/ARHP Annual Meeting

    Dietary Intake of Omega-3 Fatty Acids and Vitamin C and D Associate with Decreased Pain, Independent of Inflammation, in MTX Treated Early RA Patients

    Cecilia Lourdudoss1, Alicja Wolk2, Lars Alfredsson3, Lars Klareskog4, Ronald F. van Vollenhoven5 and Jon Lampa6, 1Dept. of Medicine, ClinTRID, Karolinska institutet, Stockholm, Sweden, 2Institute of Environmental Medicine (IMM), Karolinska institutet, Stockholm, Sweden, 3The Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden, 4Department of Medicine, Karolinska University Hospital, Stockholm, Sweden, 5Department of Medicine, Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), The Karolinska Institute, Stockholm, Sweden, 6Dep of Medicine, Rheumatology unit, Karolinska Institute, Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Chronic pain is common in RA and considered as the major disease burden from the patients’ perspective. Earlier data suggest that omega-3 fatty acids,…
  • Abstract Number: 1044 • 2015 ACR/ARHP Annual Meeting

    Many Patients with Early Rheumatoid Arthritis Want Triple Therapy: An Analysis Combining Comparative Effectiveness Research and Patients Preferences to Inform Treatment Recommendations

    Glen S. Hazlewood1,2, Claire Bombardier3, George A. Tomlinson4 and Deborah Marshall5, 1Institute of Health, Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada, 2Medicine, University of Calgary, Calgary, AB, Canada, 3Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada, 4Medicine, University Health Network, Toronto, ON, Canada, 5University of Calgary, Calgary, AB, Canada

    Background/Purpose: Growing evidence supports the efficacy of triple therapy (methotrexate + sulphasalazine + hydroxychloroquine) for controlling disease activity in patients with early rheumatoid arthritis (ERA),…
  • Abstract Number: 1577 • 2015 ACR/ARHP Annual Meeting

    Periodontal Evaluation Is Associated with Increased Likelihood of Achieving Low Disease Activity in Rheumatoid Arthritis with Methotrexate

    Melanie Rohr1, James R. O'Dell1, Abhijeet Danve2, Harlan Sayles1, Geoffrey M. Thiele3, Jeffrey Payne4 and Ted R. Mikuls5, 1University of Nebraska Medical Center, Omaha, NE, 2Rheumatology, University of Nebraska Medical Center, Omaha, NE, 3Research Services 151, Omaha VA Medical Center, Omaha, NE, 4College of Dentistry, University of Nebraska Medical Center, Lincoln, NE, 5Medicine, University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: Rheumatoid arthritis (RA) outcomes have improved substantially due to the development of new drug therapies, but also due to emphasis on early aggressive MTX…
  • Abstract Number: 1632 • 2015 ACR/ARHP Annual Meeting

    Do RA Susceptibility Loci Predict Response to Methotrexate As First DMARD in Early RA?

    Thomas Frisell1, Saedis Saevarsdottir2,3 and Johan Askling1,4, 1Clinical Epidemiology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden, 2Rheumatology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 3Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden, 4Rheumatology Unit, Karolinska University Hospital, Stockholm, Sweden

    Background/Purpose: Improved means to predict which RA patients will respond to methotrexate monotherapy, the preferred first line therapy in early RA, would allow patients to…
  • Abstract Number: 1640 • 2015 ACR/ARHP Annual Meeting

    Effect of Methotrexate Dose on the Efficacy of Tofacitinib: Treatment Outcomes from a Phase 3 Clinical Trial of Patients with Rheumatoid Arthritis

    Roy Fleischmann1, Philip J. Mease2, Sergio Schwartzman3, Lie-Ju Hwang4, Aditya Patel5, Koshika Soma4, Carol A. Connell6, Liza Takiya4 and Eustratios Bananis7, 1Rheumatology, Metroplex Clinical Research Center, Dallas, TX, 2Rheumatology Research, Swedish Medical Center, Seattle, WA, 3Hospital for Special Surgery, New York, NY, 4Pfizer Inc, New York, NY, 5Inventiv Health Inc, South Plainfield, NJ, 6Pfizer Inc, Groton, CT, 7Pfizer Inc, Collegeville, PA

    Background/Purpose: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). ORAL Scan was a 2-year, randomized, Phase 3, clinical trial…
  • Abstract Number: 1997 • 2015 ACR/ARHP Annual Meeting

    Underuse of Methotrexate (MTX) in the Treatment of Rheumatoid Arthritis (RA) in the United States (US): Results of a Comprehensive Pharmaceutical Claims Analysis

    James R. O'Dell1, Melanie Rohr1, Stanley B. Cohen2, J Carter Thorne3 and Ted R. Mikuls1, 1University of Nebraska Medical Center, Omaha, NE, 2Metroplex Clinical Research Center, Dallas, TX, 3Southlake Regional Health Centre, Newmarket, ON, Canada

    Background/Purpose: MTX is the anchor DMARD for RA treatment, but there is limited information about its appropriate use in clinical practice. This claims analysis was…
  • Abstract Number: 2138 • 2015 ACR/ARHP Annual Meeting

    Safety and Efficacy Results of a Phase 2, Double-Blind, Placebo-Controlled Clinical Study of Duvelisib with Background Methotrexate (MTX) in Adults with Moderate-to-Severe Rheumatoid Arthritis (RA)

    Richard Leff1, Sunil Kumar2, Natalia Nikulenkova3, Igor Kaidashev4, Kerstin Allen5, Joi Dunbar6, Howard Stern7, Julian Adams6 and Michael Weinblatt8, 1Clinical Research, Infinity Pharmaceuticals, Inc., Cambridge, MA, 2Centre for Clinical Research and Effective Practice (CCRep), Auckland, New Zealand, 3State Budgetary Healthcare Institution of Vladimir Region, Regional Clinical Hospital, Vladimir, Russia, 4City Clinical Hospital #1 of Poltava City, Poltava, Ukraine, 5Biostatistics, Infinity Pharmaceuticals, Inc., Cambridge, MA, 6Infinity Pharmaceuticals, Inc., Cambridge, MA, 7Translational Science, Infinity Pharmaceuticals, Inc., Cambridge, MA, 8Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA

    Background/Purpose:  Duvelisib is a potent, oral, dual inhibitor of phosphoinositide-3-kinase (PI3K)-δ,γ being developed for hematologic malignancies, and was also explored in early phase studies in…
  • Abstract Number: 187 • 2015 ACR/ARHP Annual Meeting

    Detection of Power Doppler Ultrasound Signals in Rheumatic Diseases Using Superb Microvascular Imaging (SMI): Comparison with Conventional Power Doppler Ultrasound

    Kazuhiro Yokota1, Takuma Tsuzuki Wada2, Yuji Akiyama2 and Toshihide Mimura3, 1Department of Rheumatology & Applied Immunology, Faculty of Medicine, Saitama Medical University, Irama, Japan, 2Department of Rheumatology & Applied Immunology, Faculty of Medicine, Saitama Medical University, Iruma, Japan, 3Department of Rheumatology and Applied Immunology, Faculty of Medicine, Saitama Medical University, Saitama, Japan

    Background/Purpose: The detection of power Doppler (PD) ultrasound signals in joints may be considered as the presence of joint inflammation, i.e., synovitis which is a…
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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.).

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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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