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Abstracts tagged "cyclophosphamide"

  • Abstract Number: 2675 • 2013 ACR/ARHP Annual Meeting

    Phase 2 Trial On Triptorelin For Ovary Protection In Childhood-Onset Systemic Lupus Erythematosus

    Rina Mina1, Andreas Reiff2, Clovis A. Silva3, Patricia Vega Fernandez4, Gloria C. Higgins5, Lisa F. Imundo6, Marisa S. Klein-Gitelman7, Calvin Williams8, Carol A. Wallace9, Nadia E. Aikawa10, Shannen L. Nelson11, Jun Ying12, Susan R. Rose13 and Hermine Brunner14, 1Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2Division of Rheumatology, Children's Hospital Los Angeles, Los Angeles, CA, 3Children's Institute, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brazil, 4Cincinnati Children's Hospital Medica Center, CINCINNATI, OH, 5Pediatric Rheumatology Ohio State University, Nationwide Childrens Hosp, Columbus, OH, 6Pediatric and Adult Rheumatology Columbia University Medical Center, New York, NY, 7Division of Rheumatology, Children's Memorial Hospital, Chicago, IL, 8Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI, 9University of Washington School of Medicine and Seattle Children's Hospital, Seattle, WA, 10Reumatologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil, 11Rheumatology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 12Medicine-Internal Medicine-General Medicine, University of Cincinnati, Cincinnati, OH, 13Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 14PRCSG, Cincinnati, OH

    Background/Purpose: Gonadotoxicity is a known side effect of cyclophosphamide (CYC) therapy in childhood-onset systemic lupus erythematosus (cSLE).  Gonadotropin releasing hormone (GnRH) agonists, such as triptorelin,…
  • Abstract Number: 1559 • 2013 ACR/ARHP Annual Meeting

    Cyclophosphamide and Rituximab Combination Treatment For Severe Systemic Lupus erythematosus is Effective and Well Tolerated

    Ali Shahzad1, Farheen Jafri2, Bisharah Rizvi2, Xiongce Zhao3, Meryl Waldman3 and Sarfaraz A. Hasni4, 1National Institute of Arthritis, Musculoskeletal and skin diseases, NIAMS/NIH, Bethesda, MD, 2R-Research, Hamilton, NJ, 3NIDDK/NIH, Bethesda, MD, 4National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD

    Background/Purpose: Systemic lupus erythematosus (SLE) is often complicated by resistance or partial response to initial immunosuppressive regimen and flares after initial response.  Optimal management of…
  • Abstract Number: 1255 • 2013 ACR/ARHP Annual Meeting

    Ovarian Dysfunction In Adult Childhood-Onset Systemic Lupus Erythematosus Patients: A Possible Role Of Methotrexate?

    Daniel B. Araujo1, Lucas Yamakami2, Eloisa Bonfá3, Vilma S. T. Viana4, Sandra G. Pasoto5, Rosa M. Pereira4, Paulo C. Serafin2, Eduardo F. Borba6 and Clovis A. Silva7, 1Rheumatology, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo, Brazil, 2Gynecology Department, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brazil, 3Rheumatology Division, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 4Rheumatology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil, 5Rheumatology, Faculdade de Medicina da Universidade de São Paulo, Sao Paulo, Brazil, 6Rheumatology Division; University of São Paulo, São Paulo, Brazil, 7Pediatric Rheumatology Unit, University of São Paulo, São Paulo, Brazil

    Background/Purpose: Reduction of ovarian reserve has been observed in childhood-onset SLE (c-SLE) and adult SLE populations, and most of them were limited to follicle stimulating…
  • Abstract Number: 884 • 2013 ACR/ARHP Annual Meeting

    Treatment Of Lupus Nephritis With Abatacept Plus Low-Dose Pulse Cyclophosphamide Followed By Azathioprine (the Euro-Lupus Regimen): Twenty-Four Week Data From a Double-Blind Controlled Trial

    David Wofsy1, Anca Askanase2, Patricia C. Cagnoli3, W. Winn Chatham4, Gabriel Contreras5, Maria Dall'era6, Mary Anne Dooley7, Hilda Fragoso-Loyo8, David R. Karp9, Meenakshi Jolly10, Kenneth Kalunian11, Diane L. Kamen12, Iris Lee13, Marc C. Levesque14, S. Sam Lim15, Meggan Mackay16, Cesar Ramos-Remus17, Brad H. Rovin18, Tammy O. Utset19, Swamy Venuturupalli20, Robert Winchester21, Linna Ding22, Wendy Gao22, Lynette Keyes-Elstein23 and Patti Tosta24, 1Rheumatology/Immunology, University of California San Francisco and NIAID Autoimmunity Centers of Excellence, San Francisco, CA, 2NYU School of Medicine, New York, NY, 3Int Med/Div of Rheum, University of Michigan Health, Ann Arbor, MI, 4University of Alabama at Birmingham, Birmingham, AL, 5University of Miami, Miami, FL, 6Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA, 7University of North Carolina at Chapel Hill, Chapel Hill, NC, 8Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico, Mexico, 9Rheumatic Diseases Division, UT Southwestern Medical Center, Dallas, TX, 10Rheumatology, Rush University Medical Center, Chicago, IL, 11UCSD School of Medicine, La Jolla, CA, 12Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 13Nephrology, Temple University, Philadelphia, PA, 14Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, 15Emory University School of Medicine, Division of Rheumatology, Atlanta, GA, 16Autoimmune & Musculoskeletal Disease, Feinstein Institute for Medical Research, Manhasset, NY, 17Unidad de Investigacion en Enfermedades Cronico-Degenerativas, Guadalajara, Mexico, 18Division of Nephrology, Ohio State University Medical Center, Columbus, OH, 19Rheumatology, University of Chicago Medical Center, Chicago, IL, 20Cedars-Sinai Medical Center, West Hollywood, CA, 21Dept of Medicine & Pathology, Columbia University, New York, NY, 22NIAID, Bethesda, MD, 23Rho Federal Systems, Inc., Chapel Hill, NC, 24Immune Tolerance Network, San Francisco, CA

    Background/Purpose: Studies in murine models for SLE have shown that CTLA4Ig can ameliorate murine lupus nephritis.  Moreover, the combination of CTLA4Ig plus intravenous cyclophosphamide (IVC)…
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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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