Difference between revisions of "Temsirolimus (Torisel)"
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==Also known as== | ==Also known as== | ||
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| − | + | *'''Brand name:''' Torisel | |
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==References== | ==References== | ||
Revision as of 03:13, 8 June 2019
General information
Class/mechanism: mTOR (mammalian target of rapamycin) inhibitor. mTOR inhibition by temsirolimus interferes with the ability of mTOR to phosphorylate downstream targets in the PI3 kinase/AKT pathway, such as p70S6k and the S6 ribosomal protein. Temsirolimus has also been observed to reduce levels of VEGF (vascular endothelial growth factor) and hypoxia-inducible factors HIF-1 and HIF-2 alpha.[1][2][3]
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 prescribing information.[1]
Diseases for which it is used
- CNS lymphoma
- Diffuse large B-cell lymphoma
- Follicular lymphoma
- Mantle cell lymphoma
- Renal cell carcinoma
- Endometrial cancer
Patient drug information
- Temsirolimus (Torisel) patient drug information (Chemocare)[4]
- Temsirolimus (Torisel) patient drug information (UpToDate)[5]
History of changes in FDA indication
- 5/30/2007: Initial FDA approval for the treatment of advanced renal cell carcinoma.
Also known as
- Code name: CCI-779
- Brand name: Torisel