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    Targeted molecular mechanisms of epoetin alfa.

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    Authors
    Langer, Corey J
    Hirsch, Fred R
    Cortés-Funes, Hernan
    Sawyer, Stephen T
    Thatcher, Nick
    Affiliation
    Department of Medical Oncology, Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, PA 19111, USA. cj_langer@fccc.edu
    Issue Date
    2003-08
    
    Metadata
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    Abstract
    Despite therapeutic improvements and ongoing efforts to develop more efficacious therapies, the majority of lung cancer patients face a poor prognosis. Therefore, the primary goal of current treatment is palliation, improvement and maintenance of quality of life (QOL), and (modest) prolongation of survival. Anemia frequently occurs in lung cancer patients and has been associated with decreased QOL, impaired treatment outcomes, and shortened survival time. Furthermore, anemia is a causative factor of tumor hypoxia, which compromises the efficacy of chemotherapy and radiotherapy. Thus, correction of even mild anemia seems to have a beneficial effect on QOL and cancer treatment outcomes. The current article describes the basis and mechanism for the use of recombinant human erythropoietin (rHuEPO, epoetin alfa), a molecular targeted therapy, for the treatment of cancer-related anemia, with a focus on lung cancer. Epoetin alfa has proven efficacy and safety in correcting anemia and improving QOL based on numerous clinical studies and over a decade of clinical practice. In addition, emerging data show that epoetin alfa may offer potential benefits beyond treating anemia, specifically in terms of treatment outcomes and cognitive function. Future research needs to be conducted to explore the potential for epoetin alfa to improve survival time in lung cancer patients.
    Citation
    Targeted molecular mechanisms of epoetin alfa. 2003, 41 Suppl 1:S133-45 Lung Cancer
    Journal
    Lung Cancer
    URI
    http://hdl.handle.net/10541/108145
    DOI
    10.1016/S0169-5002(03)00157-0
    PubMed ID
    12867072
    Type
    Article
    Language
    en
    ISSN
    0169-5002
    ae974a485f413a2113503eed53cd6c53
    10.1016/S0169-5002(03)00157-0
    Scopus Count
    Collections
    All Christie Publications
    All Paterson Institute for Cancer Research

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