Abstract
The discovery of recombinant human granulocyte colony-stimulating factor (rHuG-CSF) and the development of filgrastim as a clinical therapeutic tool allowed physicians to broaden their scope with respect to chemotherapeutic options and goals. From the initial registration trials, filgrastim demonstrated the ability to limit the duration and severity of neutropenia and to reduce the frequency of febrile neutropenia [1, 2]. Filgrastim allowed the maintenance of dose density, enabling the completion of the full doses of chemotherapy on schedule [3]. Furthermore, it enabled the development of more aggressive regimens with increased dose densities and dose intensities.
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Renwick, W. (2012). Use of rHuG-CSF in New Chemotherapy Strategies. In: Molineux, G., Foote, M., Arvedson, T. (eds) Twenty Years of G-CSF. Milestones in Drug Therapy. Springer, Basel. https://doi.org/10.1007/978-3-0348-0218-5_13
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