Difference between revisions of "Filgrastim (Neupogen)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*2/20/1991: Initial FDA approval.
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*1991-02-20: Initial approval.
*Currently approved to:
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*Uncertain date: Approved to decrease the incidence of infection‚ as manifested by febrile neutropenia‚ in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a significant incidence of severe neutropenia with fever.
**"Decrease the incidence of infection‚ as manifested by febrile neutropenia‚ in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a significant incidence of severe neutropenia with fever"
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*Uncertain date: Approved to reduce the time to neutrophil recovery and the duration of fever, following induction or consolidation chemotherapy treatment of patients with acute myeloid leukemia (AML).
**"Reduce the time to neutrophil recovery and the duration of fever, following induction or consolidation chemotherapy treatment of patients with acute myeloid leukemia (AML)"
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*Uncertain date: Approved to reduce the duration of neutropenia and neutropenia-related clinical sequelae‚ e.g.‚ febrile neutropenia, in patients with nonmyeloid malignancies undergoing myeloablative chemotherapy followed by bone marrow transplantation (BMT).
**"Reduce the duration of neutropenia and neutropenia-related clinical sequelae‚ e.g.‚ febrile neutropenia, in patients with nonmyeloid malignancies undergoing myeloablative chemotherapy followed by bone marrow transplantation (BMT)"
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*Uncertain date: Approved to mobilize autologous hematopoietic progenitor cells into the peripheral blood for collection by leukapheresis.
**"Mobilize autologous hematopoietic progenitor cells into the peripheral blood for collection by leukapheresis"
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*Uncertain date: Approved to reduce the incidence and duration of sequelae of severe neutropenia (e.g.‚fever‚ infections‚ oropharyngeal ulcers) in symptomatic patients with congenital neutropenia‚ cyclic neutropenia‚ or idiopathic neutropenia.
**"Reduce the incidence and duration of sequelae of severe neutropenia (e.g.‚fever‚ infections‚ oropharyngeal ulcers) in symptomatic patients with congenital neutropenia‚ cyclic neutropenia‚ or idiopathic neutropenia"
 
  
 
==Also known as==
 
==Also known as==

Revision as of 16:55, 9 May 2023

General information

Class/mechanism: Recombinant human granulocyte colony-stimulating factor (G-CSF). Binds to cell surface receptors on hematopoietic cells and stimulates proliferation‚ differentiation, and some end-cell functional activation.[1][2][3]
Route: SC, IV
Extravasation: no known issues

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.[1]

Diseases for which it is used

Note that colony stimulating factors are used for their adjuvant effect e.g. removing leukemia stem cells from their protective niches; they are not thought to have inherent anti-cancer activity.

Patient drug information

History of changes in FDA indication

  • 1991-02-20: Initial approval.
  • Uncertain date: Approved to decrease the incidence of infection‚ as manifested by febrile neutropenia‚ in patients with nonmyeloid malignancies receiving myelosuppressive anticancer drugs associated with a significant incidence of severe neutropenia with fever.
  • Uncertain date: Approved to reduce the time to neutrophil recovery and the duration of fever, following induction or consolidation chemotherapy treatment of patients with acute myeloid leukemia (AML).
  • Uncertain date: Approved to reduce the duration of neutropenia and neutropenia-related clinical sequelae‚ e.g.‚ febrile neutropenia, in patients with nonmyeloid malignancies undergoing myeloablative chemotherapy followed by bone marrow transplantation (BMT).
  • Uncertain date: Approved to mobilize autologous hematopoietic progenitor cells into the peripheral blood for collection by leukapheresis.
  • Uncertain date: Approved to reduce the incidence and duration of sequelae of severe neutropenia (e.g.‚fever‚ infections‚ oropharyngeal ulcers) in symptomatic patients with congenital neutropenia‚ cyclic neutropenia‚ or idiopathic neutropenia.

Also known as

  • Generic names: filgrastim, GCSF, G-CSF, granulocyte colony stimulating factor
  • Brand names:
Synonyms
Biocilin Biofigran Biofilgran Euprotin Filatil Filgen Filgrastima Gran
Granulokine Grasalva Grasin Grastim Leicita Leubene Leucin Leucocim
Leucokain Leucostim Leukokine Leumostin Lioplim Mielastra Myelostim Neipogen
Neitrostim Neukine Neupogen Nevkine Topneuter

References