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Novel erythropoiesis stimulating protein (NESP) for the treatment of anaemia of chronic disease associated with cancer
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  • Published: 03 April 2001

Novel erythropoiesis stimulating protein (NESP) for the treatment of anaemia of chronic disease associated with cancer

  • R E Smith Jr1,
  • I A Jaiyesimi2,
  • L A Meza3,
  • N S Tchekmedyian4,
  • D Chan5,
  • H Griffith6,
  • S Brosman7,
  • R Bukowski8,
  • M Murdoch9,
  • M Rarick10,
  • A Saven11,
  • A B Colowick12,
  • A Fleishman13,
  • U Gayko14 &
  • …
  • J Glaspy15 

British Journal of Cancer volume 84, pages 24–30 (2001)Cite this article

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Abstract

Anaemia is a common haematologic disorder in patients with cancer and has a multifactorial aetiology, including the effects of the malignancy itself and residual effects from previous therapy. Novel erythropoiesis stimulating protein (NESP, darbepoetin alfa), a protein with additional sialic acid compared with erythropoietin (EPO), stimulates erythropoiesis by the same mechanism as recombinant human erythropoietin (rHuEPO) but it is biochemically distinct. NESP, with its approximately 3-fold greater serum half-life, can maintain haemoglobin levels as effectively as rHuEPO in anaemic patients with chronic renal failure and do so with less frequent dosing. We investigated the ability of NESP to safely increase haemoglobin levels of anaemic patients with non-myeloid malignancies not receiving chemotherapy. NESP was administered under the supervision of a physician at doses of 0.5, 1.0, 2.25 or 4.5 mcg kg–1wk–1for a maximum of 12 weeks. This report includes 89 patients completing the study by November 2000. NESP was well tolerated, with no reported dose-limiting toxicities or treatment-related severe adverse events. Increasing doses of NESP corresponded with increased efficacy. The percentage (95% confidence interval) of patients responding ranged from 61% (42%, 77%) in the 1.0 mcg kg–1wk–1group to 83% (65%, 94%) in the 4.5 mcg kg–1wk–1group. © 2001 Cancer Research Campaign

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. South Carolina Oncology Associates, 1301 Taylor, Suite IA, Columbia, SC 29201, USA

    R E Smith Jr

  2. William Beaumont Hospital, 3577 West 13 Mile Road, Suite 40, Royal Oak, MI 48073, USA

    I A Jaiyesimi

  3. Southwest Oncology Associates, 443 Heymann Blvd, Suite A, Lafayette, LA 70503, USA

    L A Meza

  4. Pacific Shores Medical Group Inc, 1043 Elm Ave, Suite 104, Long Beach, CA 90813-3244, USA

    N S Tchekmedyian

  5. Cancer Care Associates Medical Group, 514 North Prospect St, Redondo Beach, CA 90277-3026, USA

    D Chan

  6. Memorial Clinic Research Center, 520 Lilly Road, NE Building 3, Olympia, WA 98506, USA

    H Griffith

  7. Pacific Clinical Research, 1260 15th Street, Suite 1200, Santa Monica, CA 90404, USA

    S Brosman

  8. The Cleveland Clinic Foundation, Desk S33, 9500 Euclid Avenue, Cleveland, OH 44195, USA

    R Bukowski

  9. Urology Associates, 7500 Hanover Parkway, Suite 206, Greenbelt, MD 20770, USA

    M Murdoch

  10. Kaiser Permanente Northwest Division, 3600 North Interstate, Portland, OR 97227, USA

    M Rarick

  11. Scripps Clinic, 10666 North Torrey Pines Road, La Jolla, CA 92037, USA

    A Saven

  12. Amgen Inc, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, USA

    A B Colowick

  13. Amgen Inc, One Amgen Center Drive, M/S 24-1-C, Thousand Oaks, CA 91320-1799, USA

    A Fleishman

  14. Amgen Inc, One Amgen Center Drive; M/S 24-1-C, Thousand Oaks, CA 91320-1799, USA

    U Gayko

  15. UCLA School of Medicine, 200 Medical Plaza, Suite 120, Los Angeles, CA 90024, USA

    J Glaspy

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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Smith, R., Jaiyesimi, I., Meza, L. et al. Novel erythropoiesis stimulating protein (NESP) for the treatment of anaemia of chronic disease associated with cancer. Br J Cancer 84 (Suppl 1), 24–30 (2001). https://doi.org/10.1054/bjoc.2001.1749

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  • Published: 03 April 2001

  • Issue date: 01 April 2001

  • DOI: https://doi.org/10.1054/bjoc.2001.1749

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Keywords

  • anaemia
  • cancer
  • chemotherapy
  • chronic disease
  • darbepoetin alfa
  • erythropoietin

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Improving the Standard of Care in the Management of Cancer-Related Anaemia: Focus on Darbepoetin Alfa, a Novel Erythropoiesis Stimulating Protein

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