Difference between revisions of "Denileukin diftitox (Ontak)"

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==Diseases for which it is used==
 
==Diseases for which it is used==
*[[T-cell lymphoma|Cutaneous T-cell lymphoma (CTCL)]]
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*[[Cutaneous T-cell lymphoma]]
  
 
==Patient drug information==
 
==Patient drug information==
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==History of changes in FDA indication==
 
==History of changes in FDA indication==
* 2/5/1999: Initial FDA approval "for the treatment of patients with persistent or recurrent [[T-cell lymphoma | cutaneous T-cell lymphoma]] whose malignant cells express the CD25 component of the IL-2 receptor."
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* 2/5/1999: Initial FDA approval "for the treatment of patients with persistent or recurrent [[Cutaneous T-cell lymphoma | cutaneous T-cell lymphoma]] whose malignant cells express the CD25 component of the IL-2 receptor."
 
   
 
   
 
==References==
 
==References==
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[[Category:Immunotoxin]]
 
[[Category:Immunotoxin]]
  
[[Category:T-cell lymphoma medications]]
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[[Category:Cutaneous T-cell lymphoma medications]]
  
 
[[Category:Drugs FDA approved in 1999]]
 
[[Category:Drugs FDA approved in 1999]]

Revision as of 14:49, 14 December 2014

General information

Class/mechanism: Recombinant diphtheria toxin fusion protein which binds with high affinity to IL-2 receptors. The fusion protein is internalized by receptor-mediated endocytosis and is cleaved, releasing the diphtheria toxin, which inhibits protein synthesis and causes cell death.[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

Patient drug information

History of changes in FDA indication

  • 2/5/1999: Initial FDA approval "for the treatment of patients with persistent or recurrent cutaneous T-cell lymphoma whose malignant cells express the CD25 component of the IL-2 receptor."

References