Difference between revisions of "Omacetaxine (Synribo)"

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==General information==
 
==General information==
Class/mechanism: Cephalotaxine ester & natural alkaloid that inhibits protein synthesis/translation/elongation; prepared via a semi-synthetic process from cephalotaxine, an extract of Cephalotaxus species leaves.  Mechanism is not fully understood, but omacetaxine mepesuccinate inhibits protein synthesis and promotes apoptosis in a manner that does not involve direct binding of Bcr-Abl.  Omacetaxine mepesuccinate has been observed to bind to the A-site cleft in the large ribosomal subunit of a type of archaeabacteria.  It reduces levels of Bcr-Abl and human induced myeloid leukemia cell differentiation protein Mcl-1, an anti-apoptotic Bcl-2 family member.  Omacetaxine mepesuccinate has been seen to have activity in mouse models with wild-type Bcr-Abl, as well as imatinib-resistant chronic myeloid leukemia (CML) models with the T315I mutation.<ref name="insert">[http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/203585lbl.pdf Omacetaxine mepesuccinate (Synribo) package insert]</ref><ref>[[Media:Omacetaxine.pdf | Omacetaxine mepesuccinate (Synribo) package insert (locally hosted backup)]]</ref><ref>Quintás-Cardama A, Kantarjian H, Cortes J. Homoharringtonine, omacetaxine mepesuccinate, and chronic myeloid leukemia circa 2009. Cancer. 2009 Dec 1;115(23):5382-93. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.24601/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/19739234 PubMed]</ref>
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Class/mechanism: Cephalotaxine ester & natural alkaloid that inhibits protein synthesis/translation/elongation; prepared via a semi-synthetic process from cephalotaxine, an extract of Cephalotaxus species leaves.  Mechanism is not fully understood, but omacetaxine mepesuccinate inhibits protein synthesis and promotes apoptosis in a manner that does not involve direct binding of Bcr-Abl.  Omacetaxine mepesuccinate has been observed to bind to the A-site cleft in the large ribosomal subunit of a type of archaeabacteria.  It reduces levels of Bcr-Abl and human induced myeloid leukemia cell differentiation protein Mcl-1, an anti-apoptotic Bcl-2 family member.  Omacetaxine mepesuccinate has been seen to have activity in mouse models with wild-type Bcr-Abl, as well as imatinib-resistant chronic myeloid leukemia (CML) models with the T315I mutation.<ref name="insert">[http://synribo.com/pdf/synribo_pi.pdf Omacetaxine mepesuccinate (Synribo) package insert]</ref><ref>[[Media:Omacetaxine.pdf | Omacetaxine mepesuccinate (Synribo) package insert (locally hosted backup)]]</ref><ref>[http://synribo.com/ Synribo manufacturer's website]</ref><ref>Quintás-Cardama A, Kantarjian H, Cortes J. Homoharringtonine, omacetaxine mepesuccinate, and chronic myeloid leukemia circa 2009. Cancer. 2009 Dec 1;115(23):5382-93. [http://onlinelibrary.wiley.com/doi/10.1002/cncr.24601/full link to original article] [http://www.ncbi.nlm.nih.gov/pubmed/19739234 PubMed]</ref>
  
 
Route: IV, SC
 
Route: IV, SC
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==Patient drug information==
 
==Patient drug information==
*Brief patient counseling information can be found on [http://www.accessdata.fda.gov/drugsatfda_docs/label/2012/203585lbl.pdf#page=10 page 10 of the Omacetaxine mepesuccinate (Synribo) package insert]<ref name="insert"></ref>
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*Brief patient counseling information can be found on [http://synribo.com/pdf/synribo_pi.pdf#page=10 page 10 of the Omacetaxine mepesuccinate (Synribo) package insert]<ref name="insert"></ref>
  
 
==History of changes in FDA indication==
 
==History of changes in FDA indication==

Revision as of 02:29, 29 October 2012

FDA approved 10/26/2012. Also known as HHT, homoharringtonine, Omapro, or omacetaxine mepesuccinate.

General information

Class/mechanism: Cephalotaxine ester & natural alkaloid that inhibits protein synthesis/translation/elongation; prepared via a semi-synthetic process from cephalotaxine, an extract of Cephalotaxus species leaves. Mechanism is not fully understood, but omacetaxine mepesuccinate inhibits protein synthesis and promotes apoptosis in a manner that does not involve direct binding of Bcr-Abl. Omacetaxine mepesuccinate has been observed to bind to the A-site cleft in the large ribosomal subunit of a type of archaeabacteria. It reduces levels of Bcr-Abl and human induced myeloid leukemia cell differentiation protein Mcl-1, an anti-apoptotic Bcl-2 family member. Omacetaxine mepesuccinate has been seen to have activity in mouse models with wild-type Bcr-Abl, as well as imatinib-resistant chronic myeloid leukemia (CML) models with the T315I mutation.[1][2][3][4]

Route: IV, SC
Extravasation: no information

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 used

Clinical trials

Patient drug information

History of changes in FDA indication

  • 10/26/2012: FDA approved for "treatment of adult patients with chronic or accelerated phase chronic myeloid leukemia (CML) with resistance and/or intolerance to two or more tyrosine kinase inhibitors (TKI)."[1]

References

  1. 1.0 1.1 1.2 1.3 Omacetaxine mepesuccinate (Synribo) package insert
  2. Omacetaxine mepesuccinate (Synribo) package insert (locally hosted backup)
  3. Synribo manufacturer's website
  4. Quintás-Cardama A, Kantarjian H, Cortes J. Homoharringtonine, omacetaxine mepesuccinate, and chronic myeloid leukemia circa 2009. Cancer. 2009 Dec 1;115(23):5382-93. link to original article PubMed
  5. Cortes J, Lipton JH, Rea D, Digumarti R, Chuah C, Nanda N, Benichou AC, Craig AR, Michallet M, Nicolini FE, Kantarjian H; on behalf of the Omacetaxine 202 Study Group. Phase 2 study of subcutaneous omacetaxine mepesuccinate after TKI failure in patients with chronic-phase CML with T315I mutation. Blood. 2012 Sep 27;120(13):2573-2580. Epub 2012 Aug 15. link to original article contains verified protocol PubMed