Difference between revisions of "Melphalan (Alkeran)"

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*[[Acute promyelocytic leukemia]]
 
*[[Acute promyelocytic leukemia]]
 
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*[[Classical Hodgkin lymphoma]]
 
*[[Neuroblastoma]]
 
*[[Neuroblastoma]]
 
*Non-Hodgkin lymphoma
 
*Non-Hodgkin lymphoma

Revision as of 19:17, 9 June 2023

General information

Class/mechanism: Nitrogen mustard, alkylator. Melphalan is a bischloroethylamine alkylating agent that crosslinks DNA by binding at the N7 position of guanine, with activity against resting and proliferating cells.[1][2]
Route: IV, PO
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

Diseases for which it was used

Patient drug information

History of changes in FDA indication

  • 1964-01-17: Initial FDA approval[5]
  • Uncertain date: Indicated for the palliative treatment of multiple myeloma. (Based on SWG01)
  • Uncertain date: Indicated for the palliation of non-resectable epithelial carcinoma of the ovary. (No supporting studies are cited)

Also known as

  • Generic names: L-PAM, L-Sacrolysin, L-Sarcolysin, MPL, phenylalanine mustard
  • Brand names: Alkeran, Alkerana, Evomela, Levofolan, Melfalan, Phelinun

References