Difference between revisions of "Bendamustine"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
As Treanda:
 
As Treanda:
* 3/20/2008: Initial FDA approval "for the treatment of patients with [[Chronic lymphocytic leukemia (CLL/SLL) | chronic lymphocytic leukemia (CLL)]]."
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* 3/20/2008: Initial FDA approval for the treatment of patients with [[Chronic lymphocytic leukemia (CLL/SLL) | chronic lymphocytic leukemia (CLL)]].
* 4/22/2009: Additional indication for "Indolent B-cell non-Hodgkin’s lymphoma (NHL) that has progressed during or within six months of treatment with [[Rituximab (Rituxan) | rituximab]] or a rituximab­ containing regimen."
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*10/31/2008: Approved for the treatment of patients with indolent B-cell non-Hodgkin’s lymphoma (NHL) that progressed during or within 6 months of treatment with [[Rituximab (Rituxan) | rituximab]] or a rituximab­ containing regimen. ''(New disease entity)''
 
As Bendeka:
 
As Bendeka:
 
* 12/7/2015: Bendamustine (Bendeka) formulation FDA approved for:
 
* 12/7/2015: Bendamustine (Bendeka) formulation FDA approved for:
 
**[[Chronic lymphocytic leukemia (CLL/SLL) |Chronic lymphocytic leukemia (CLL)]]
 
**[[Chronic lymphocytic leukemia (CLL/SLL) |Chronic lymphocytic leukemia (CLL)]]
**Indolent B-cell non-Hodgkin lymphoma (NHL) that has progressed during or within six months of treatment with [[Rituximab (Rituxan)|rituximab]] or a rituximab-containing regimen."
+
**Indolent B-cell non-Hodgkin lymphoma (NHL) that has progressed during or within six months of treatment with [[Rituximab (Rituxan)|rituximab]] or a rituximab-containing regimen.
  
 
==Also known as==
 
==Also known as==

Revision as of 03:40, 27 November 2018

Note: Previous Treanda formulation discontinued on 3/31/2016 by Teva to switch to Bendeka.[1]

General information

Class/mechanism: Nitrogen mustard, alkylator; bifunctional mechlorethamine derivative containing a purine-like benzimidazole ring which forms electrophilic alkyl groups, resulting in interstrand DNA crosslinks, leading to cell death via several pathways in both quiescent and dividing cells.[2][3][4][5][6][7]
Route: IV
Extravasation: irritant (usually), vesicant (rare)

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, Medscape, UpToDate (courtesy of Lexicomp), or the prescribing information.[2]

Diseases for which it is used

Patient drug information

History of changes in FDA indication

As Treanda:

  • 3/20/2008: Initial FDA approval for the treatment of patients with chronic lymphocytic leukemia (CLL).
  • 10/31/2008: Approved for the treatment of patients with indolent B-cell non-Hodgkin’s lymphoma (NHL) that progressed during or within 6 months of treatment with rituximab or a rituximab­ containing regimen. (New disease entity)

As Bendeka:

  • 12/7/2015: Bendamustine (Bendeka) formulation FDA approved for:

Also known as

  • Code names: CEP-18083, SDX-105, SyB L-0501
  • Generic names: bendamustin hydrochloride, bendamustine hydrochloride, cytostasan hydrochloride
  • Brand names: Bendamax, Bendawel, Bendeka, Bendit, Innomustine, Leuben, Levact, Maxtorin, MyMust, Purplz, Ribomustin, Treakisym, Treanda, Xyotin

References