Difference between revisions of "Fotemustine (Muphoran)"

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==Mechanism of action==
 
==Mechanism of action==
From the [http://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=38865 NCI Drug Dictionary]: A chloroethylating nitrosourea with antineoplastic activity. Fotemustine alkylates guanine by forming chloroethyl adducts at the 6 position of guanine, resulting in N1-guanine and N3-cytosine cross linkages, inhibition of DNA synthesis, cell cycle arrest, and finally apoptosis. This agent is lipophilic and crosses the blood-brain barrier.
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=38865 NCI Drug Dictionary]: A chloroethylating nitrosourea with antineoplastic activity. Fotemustine alkylates guanine by forming chloroethyl adducts at the 6 position of guanine, resulting in N1-guanine and N3-cytosine cross linkages, inhibition of DNA synthesis, cell cycle arrest, and finally apoptosis. This agent is lipophilic and crosses the blood-brain barrier.
  
 
==Diseases for which it is used==
 
==Diseases for which it is used==
 
*[[Diffuse large B-cell lymphoma]]
 
*[[Diffuse large B-cell lymphoma]]
*[[Hodgkin lymphoma]]
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*[[Classical Hodgkin lymphoma]]
 
*[[Melanoma]]
 
*[[Melanoma]]
 
**[[CNS melanoma]]
 
**[[CNS melanoma]]
 
**[[Uveal melanoma]]
 
**[[Uveal melanoma]]
  
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==History of changes in EMA indication==
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*1989-04-14: EURD
 
==Also known as==
 
==Also known as==
 
*'''Brand names:''' Muphoran, Mustophoran
 
*'''Brand names:''' Muphoran, Mustophoran
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[[Category:Diffuse large B-cell lymphoma medications]]
 
[[Category:Diffuse large B-cell lymphoma medications]]
[[Category:Hodgkin lymphoma medications]]
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[[Category:Classical Hodgkin lymphoma medications]]
 
[[Category:Melanoma medications]]
 
[[Category:Melanoma medications]]
 
[[Category:Uveal melanoma medications]]
 
[[Category:Uveal melanoma medications]]
  
[[Category:EMA approved drugs]]
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[[Category:EMA approved in 1989]]

Latest revision as of 20:21, 27 June 2024

Mechanism of action

From the NCI Drug Dictionary: A chloroethylating nitrosourea with antineoplastic activity. Fotemustine alkylates guanine by forming chloroethyl adducts at the 6 position of guanine, resulting in N1-guanine and N3-cytosine cross linkages, inhibition of DNA synthesis, cell cycle arrest, and finally apoptosis. This agent is lipophilic and crosses the blood-brain barrier.

Diseases for which it is used

History of changes in EMA indication

  • 1989-04-14: EURD

Also known as

  • Brand names: Muphoran, Mustophoran