Difference between revisions of "Alvocidib (Flavopiridol)"

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===[[Acute myeloid leukemia]]===
 
===[[Acute myeloid leukemia]]===
 
==FLAM {{#subobject:8a86fb|Regimen=1}}==
 
==FLAM {{#subobject:8a86fb|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
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|-
 
|[[#top|back to top]]
 
|}
 
 
FLAM: '''<u>FL</u>'''avopiridol (Alvocidib), '''<u>A</u>'''ra-C (Cytarabine), '''<u>M</u>'''itoxantrone
 
FLAM: '''<u>FL</u>'''avopiridol (Alvocidib), '''<u>A</u>'''ra-C (Cytarabine), '''<u>M</u>'''itoxantrone
 
===Regimen {{#subobject:5340f1|Variant=1}}===
 
===Regimen {{#subobject:5340f1|Variant=1}}===
{| class="wikitable" style="width: 100%; text-align:center;"  
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{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 25%"|Study
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
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|-
 
|-
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800702/ Zeidner et al. 2015 (JHOC-J1101)]
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800702/ Zeidner et al. 2015 (JHOC-J1101)]
| style="background-color:#1a9851" |Randomized Phase II (E)
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| style="background-color:#1a9851" |Randomized Phase 2 (E)
 
|[[#Cytarabine_.26_Daunorubicin|7+3d, high-dose dauno]]
 
|[[#Cytarabine_.26_Daunorubicin|7+3d, high-dose dauno]]
 
| style="background-color:#1a9850" |Superior CR rate
 
| style="background-color:#1a9850" |Superior CR rate
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===References===
 
===References===
# '''JHOC-J1101:''' Zeidner JF, Foster MC, Blackford AL, Litzow MR, Morris LE, Strickland SA, Lancet JE, Bose P, Levy MY, Tibes R, Gojo I, Gocke CD, Rosner GL, Little RF, Wright JJ, Doyle LA, Smith BD, Karp JE. Randomized multicenter phase II study of flavopiridol (alvocidib), cytarabine, and mitoxantrone (FLAM) versus cytarabine/daunorubicin (7+3) in newly diagnosed acute myeloid leukemia. Haematologica. 2015 Sep;100(9):1172-9. Epub 2015 May 28. [http://www.haematologica.org/content/100/9/1172 link to original article] '''contains verified protocol''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800702/ link to PMC article] [https://www.ncbi.nlm.nih.gov/pubmed/26022709 PubMed]
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# '''JHOC-J1101:''' Zeidner JF, Foster MC, Blackford AL, Litzow MR, Morris LE, Strickland SA, Lancet JE, Bose P, Levy MY, Tibes R, Gojo I, Gocke CD, Rosner GL, Little RF, Wright JJ, Doyle LA, Smith BD, Karp JE. Randomized multicenter phase II study of flavopiridol (alvocidib), cytarabine, and mitoxantrone (FLAM) versus cytarabine/daunorubicin (7+3) in newly diagnosed acute myeloid leukemia. Haematologica. 2015 Sep;100(9):1172-9. Epub 2015 May 28. [http://www.haematologica.org/content/100/9/1172 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800702/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/26022709/ PubMed]
  
 
===[[Chronic lymphocytic leukemia]]===
 
===[[Chronic lymphocytic leukemia]]===
 
==History of changes in FDA indication==
 
*4/13/2007: Granted orphan status for treatment of [[Chronic lymphocytic leukemia | B-cell chronic lymphocytic leukemia (B-CLL)]] or prolymphocytic leukemia arising from CLL.
 
*4/23/2014: Granted orphan designation for the treatment of patients with [[Acute myeloid leukemia | acute myeloid leukemia (AML)]]
 
  
 
==Also known as==
 
==Also known as==
 
*'''Generic name:''' flavopiridol
 
*'''Generic name:''' flavopiridol
*'''Code names:''' HMR 1275, L-868275
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*'''Code names:''' HMR-1275, L-868275
  
 
[[Category:Drugs]]
 
[[Category:Drugs]]
 
[[Category:Oral medications]]
 
[[Category:Oral medications]]
 
[[Category:Kinase inhibitors]]
 
 
[[Category:CDK inhibitors]]
 
[[Category:CDK inhibitors]]
  
[[Category:Orphan drug]]
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[[Category:Acute myeloid leukemia medications (investigational)]]
 +
[[Category:Chronic lymphocytic leukemia medications (investigational)]]
 
[[Category:Investigational drugs]]
 
[[Category:Investigational drugs]]

Revision as of 02:06, 11 August 2023

Mechanism of action

From the NCI Drug Dictionary: A synthetic N-methylpiperidinyl chlorophenyl flavone compound. As an inhibitor of cyclin-dependent kinase, alvocidib induces cell cycle arrest by preventing phosphorylation of cyclin-dependent kinases (CDKs) and by down-regulating cyclin D1 and D3 expression, resulting in G1 cell cycle arrest and apoptosis.
Route: PO

Preliminary data

Acute myeloid leukemia

FLAM

FLAM: FLavopiridol (Alvocidib), Ara-C (Cytarabine), Mitoxantrone

Regimen

Study Evidence Comparator Comparative Efficacy
Zeidner et al. 2015 (JHOC-J1101) Randomized Phase 2 (E) 7+3d, high-dose dauno Superior CR rate

Chemotherapy

One course

References

  1. JHOC-J1101: Zeidner JF, Foster MC, Blackford AL, Litzow MR, Morris LE, Strickland SA, Lancet JE, Bose P, Levy MY, Tibes R, Gojo I, Gocke CD, Rosner GL, Little RF, Wright JJ, Doyle LA, Smith BD, Karp JE. Randomized multicenter phase II study of flavopiridol (alvocidib), cytarabine, and mitoxantrone (FLAM) versus cytarabine/daunorubicin (7+3) in newly diagnosed acute myeloid leukemia. Haematologica. 2015 Sep;100(9):1172-9. Epub 2015 May 28. link to original article contains dosing details in manuscript link to PMC article PubMed

Chronic lymphocytic leukemia

Also known as

  • Generic name: flavopiridol
  • Code names: HMR-1275, L-868275