Difference between revisions of "Cetuximab (Erbitux)"

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m (Created page with "==General information== Class/mechanism: Causes damage or degradation of PML-RAR alpha fusion protein, causes apoptosis-type changes in NB4 human promyelocytic leukemia cells in ...")
 
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==General information==
 
==General information==
Class/mechanism: Causes damage or degradation of PML-RAR alpha fusion protein, causes apoptosis-type changes in NB4 human promyelocytic leukemia cells in vitro.<ref name="insert">[http://packageinserts.bms.com/pi/pi_erbitux.pdf Cetuximab (Erbitux) package insert]</ref><ref>[http://hemonc.org/docs/packageinsert/cetuximab.pdf Cetuximab (Erbitux) package insert (locally hosted backup)]</ref>
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Class/mechanism: EGFR antagonist; monoclonal antibody that binds to the EGFR/HER1/c-ErbB-1 receptor tyrosine kinase, competitively inhibiting binding of epidermal growth factor (EGF) and other ligands, such as transforming growth factor-alpha.  This results in inhibition of cell growth, induction of apoptosis, decreased matrix metalloproteinase, and decreased vascular endothelial growth factor production.<ref name="insert">[http://packageinserts.bms.com/pi/pi_erbitux.pdf Cetuximab (Erbitux) package insert]</ref><ref>[http://hemonc.org/docs/packageinsert/cetuximab.pdf Cetuximab (Erbitux) package insert (locally hosted backup)]</ref>
 
<br>Route: IV
 
<br>Route: IV
 
<br>Extravasation: no information
 
<br>Extravasation: no information

Revision as of 05:16, 30 November 2011

General information

Class/mechanism: EGFR antagonist; monoclonal antibody that binds to the EGFR/HER1/c-ErbB-1 receptor tyrosine kinase, competitively inhibiting binding of epidermal growth factor (EGF) and other ligands, such as transforming growth factor-alpha. This results in inhibition of cell growth, induction of apoptosis, decreased matrix metalloproteinase, and decreased vascular endothelial growth factor production.[1][2]
Route: IV
Extravasation: no information

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 package insert[1].

Patient drug information

Regimens

Standard format will be:
<acronym (if any)> <generic drug1, generic drug2, generic drug3, etc.> (disease)

References