Chemical Property of Sargramostim
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Chemical Property:
- Purity/Quality:
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99% *data from raw suppliers
rHuGM-CSF *data from reagent suppliers
Safty Information:
- Pictogram(s):
- Hazard Codes:
- MSDS Files:
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Useful:
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Description
Sargramostim, a recombinant DNA product, is a granulocyte macrophage colony
stimulating factor (GM-CSF) indicated for the treatment of cancer patients after
autologous bone marrow transplants. It stimulates immature cells to develop into
granulocytes and macrophages and can also switch on mature granulocytes and
macrophages.Other indications include improved bone m m w recovery in
non-Hodgkins lymphoma and acute lymphoblastic leukemia.
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Uses
Antineutropenic; hematopoietic stimulant.
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Indications
Sargramostim (GM-CSF, Leukine, Prokine) is a human
recombinant granulocyte and macrophage colony–
stimulating factor that stimulates the production and potentiates
the function of both granulocytes and macrophages
from hematopoietic progenitor cells. It is used to
accelerate bone marrow repopulation after high-dose
chemotherapy, radiation therapy, and bone marrow transplantation.
Adverse effects associated with sargramostim
use include bone pain (similar to that of filgrastim), fatigue,
fevers, skin rash, malaise, and fluid retention.
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Clinical Use
Sargramostim binds to specific receptors on target cellsand induces proliferation, activation, and maturation.Administration to patients causes a dose-related increase inthe peripheral white blood cell count. Unlike G-CSF, GMCSFis a multilineage hematopoietic growth factor that inducespartially committed progenitor cells to proliferate anddifferentiate along the granulocyte and the macrophage pathways.It also enhances the function of mature granulocytesand macrophages/monocytes. GM-CSF increases the chemotactic,antifungal, and antiparasitic activities of granulocytesand monocytes. It also increases the cytotoxicity of monocytestoward neoplastic cell lines and activates polymorphonuclearleukocytes to inhibit the growth of tumor cells.Sargramostim is used to reconstitute the myeloid tissueafter autologous bone marrow transplant and followingchemotherapy in acute myelogenous leukemia. The preparationdecreases the incidence of infection, decreases the numberof days that antibiotics are required, and decreases theduration of hospital stays.