Difference between revisions of "Cladribine (Leustatin)"

From HemOnc.org - A Hematology Oncology Wiki
Jump to navigation Jump to search
Line 26: Line 26:
  
 
==History of changes in FDA indication==
 
==History of changes in FDA indication==
* 2/26/1993: Initial FDA approval for treatment of active [[hairy cell leukemia]]. ''(Based on Saven et al. 1998)''
+
* 1993-02-26: Initial FDA approval for treatment of active [[hairy cell leukemia]]. ''(Based on Saven et al. 1998)''
  
 
==Also known as==
 
==Also known as==

Revision as of 20:51, 4 May 2023

General information

Class/mechanism: Purine analog; mimics the nucleoside adenosine, inhibiting adenosine deaminase, which interferes with DNA synthesis and repair.[1][2]
Route: IV, SC
Extravasation: irritant or neutral, depending on reference

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 established (work in progress)

Diseases for which it is used

Patient drug information

History of changes in FDA indication

  • 1993-02-26: Initial FDA approval for treatment of active hairy cell leukemia. (Based on Saven et al. 1998)

Also known as

  • Generic names: 2-chlorodeoxyadenosine, 2-CdA
  • Brand names: Leustatin, Litak, Movectro

References