Difference between revisions of "Perifosine (KRX-0401)"

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==Mechanism of action==
 
==Mechanism of action==
AKT and PI3K inhibitor
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=43408 NCI Drug Dictionary]: An orally active alkyl-phosphocholine compound with potential antineoplastic activity. Targeting cellular membranes, perifosine modulates membrane permeability, membrane lipid composition, phospholipid metabolism, and mitogenic signal transduction, resulting in cell differentiation and inhibition of cell growth. This agent also inhibits the anti-apoptotic mitogen-activated protein kinase (MAPK) pathway and modulates the balance between the MAPK and pro-apoptotic stress-activated protein kinase (SAPK/JNK) pathways, thereby inducing apoptosis.
  
 
==Preliminary data==
 
==Preliminary data==
  
===[[Hodgkin lymphoma]]===
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===[[Classical Hodgkin lymphoma]]===
# Guidetti A, Carlo-Stella C, Locatelli SL, Malorni W, Mortarini R, Viviani S, Russo D, Marchianò A, Sorasio R, Dodero A, Farina L, Giordano L, Di Nicola M, Anichini A, Corradini P, Gianni AM. Phase II Study of Perifosine and Sorafenib Dual-Targeted Therapy in Patients with Relapsed or Refractory Lymphoproliferative Diseases. Clin Cancer Res. 2014 Sep 19. [Epub ahead of print] [http://clincancerres.aacrjournals.org/content/20/22/5641.full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/25239609 PubMed]
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# Guidetti A, Carlo-Stella C, Locatelli SL, Malorni W, Mortarini R, Viviani S, Russo D, Marchianò A, Sorasio R, Dodero A, Farina L, Giordano L, Di Nicola M, Anichini A, Corradini P, Gianni AM. Phase II Study of Perifosine and Sorafenib Dual-Targeted Therapy in Patients with Relapsed or Refractory Lymphoproliferative Diseases. Clin Cancer Res. 2014 Nov 15;20(22):5641-51. Epub 2014 Sep 19. [http://clincancerres.aacrjournals.org/content/20/22/5641.full link to original article] [https://pubmed.ncbi.nlm.nih.gov/25239609/ PubMed]
  
==History of changes in FDA indication==
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==Also known as==
* 9/3/2009: Received FDA orphan drug designation for treatment of [[Multiple myeloma | multiple myeloma]].
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*'''Code name:''' KRX-0401
* 7/9/2010: Received FDA orphan drug designation for treatment of [[Neuroblastoma | neuroblastoma]].
 
  
[[Category:Drug index]]
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[[Category:Drugs]]
[[Category:Chemotherapy]]
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[[Category:Oral medications]]
  
[[Category:Kinase inhibitors]]
 
 
[[Category:AKT1 inhibitors]]
 
[[Category:AKT1 inhibitors]]
[[Category:PI3K inhibitors]]
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[[Category:MEK inhibitors]]
  
[[Category:Investigational]]
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[[Category:Investigational drugs]]
[[Category:Orphan drug]]
 

Latest revision as of 01:02, 15 June 2023

Mechanism of action

From the NCI Drug Dictionary: An orally active alkyl-phosphocholine compound with potential antineoplastic activity. Targeting cellular membranes, perifosine modulates membrane permeability, membrane lipid composition, phospholipid metabolism, and mitogenic signal transduction, resulting in cell differentiation and inhibition of cell growth. This agent also inhibits the anti-apoptotic mitogen-activated protein kinase (MAPK) pathway and modulates the balance between the MAPK and pro-apoptotic stress-activated protein kinase (SAPK/JNK) pathways, thereby inducing apoptosis.

Preliminary data

Classical Hodgkin lymphoma

  1. Guidetti A, Carlo-Stella C, Locatelli SL, Malorni W, Mortarini R, Viviani S, Russo D, Marchianò A, Sorasio R, Dodero A, Farina L, Giordano L, Di Nicola M, Anichini A, Corradini P, Gianni AM. Phase II Study of Perifosine and Sorafenib Dual-Targeted Therapy in Patients with Relapsed or Refractory Lymphoproliferative Diseases. Clin Cancer Res. 2014 Nov 15;20(22):5641-51. Epub 2014 Sep 19. link to original article PubMed

Also known as

  • Code name: KRX-0401