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Darbepoetin alpha in the treatment of cancer chemotherapy-induced anemia
Author(s) -
Alberto Grossi,
Francesca Balestri,
Simone Santini
Publication year - 2007
Publication title -
therapeutics and clinical risk management
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.719
H-Index - 55
eISSN - 1178-203X
pISSN - 1176-6336
DOI - 10.2147/tcrm.2007.3.2.269
Subject(s) - medicine , anemia , darbepoetin alfa , erythropoietin , cancer , quality of life (healthcare) , alpha (finance) , chemotherapy , radiation therapy , pharmacodynamics , pharmacokinetics , hemoglobin , oncology , intensive care medicine , surgery , construct validity , nursing , patient satisfaction
Anemia is a common, but underestimated and undertreated, complication of patients with cancer receiving chemo- or radiotherapy, and negatively affects their quality of life (QoL). Erythropoietic proteins (EPS) offer an effective treatment of cancer anemia and ameliorate QoL, although their use requires the correct targeting of hemoglobin increase to avoid thromboembolic complications. Currently the effort is focused on offering patients this effective treatment with reduced frequency of administration. Higher weekly single doses of recombinant human Epo (rHuEpo) either alpha or beta, instead of three times per week, have been proposed for the treatment. The pharmacokinetic and pharmacodynamic characteristics of the hyperglycosylated protein darbepoetin alpha permit even longer inter vals between administrations. Every other week or every three weeks schedules have shown results (erythropoietic response, reduction of transfusion requirements, and improvement of QoL) comparable with those of weekly rHuEpo.

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