Etoposide

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Etoposide
Etoposide.svg
Etoposide ball-and-stick.png
Clinical data
Pronunciation/ˌɛtoʊˈpoʊsaɪd/
Trade namesEtopophos, Toposar, Vepesid, others
Other namesVP-16; VP-16-213
AHFS/Drugs.comMonograph
MedlinePlusa684055
Pregnancy
category
  • AU: D
Routes of
administration		By mouth, intravenous
ATC code
Legal status
Legal status
Pharmacokinetic data
BioavailabilityHighly variable, 25 to 75%
Protein binding97%
MetabolismLiver (CYP3A4 involved)
Elimination half-lifeOral: 6 h., IV: 6-12 h., IV in children: 3 h.
ExcretionKidney and fecal
Identifiers
  • 4'-Demethyl-epipodophyllotoxin 9-[4,6-O-(R)-ethylidene-beta-D-glucopyranoside], 4' -(dihydrogen phosphate)
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.046.812 Edit this at Wikidata
Chemical and physical data
FormulaC29H32O13
Molar mass588.562 g·mol−1
3D model (JSmol)
Melting point243.5 °C (470.3 °F)
  • C[C@@H]1OC[C@@H]2[C@@H](O1)[C@@H]([C@H]([C@@H](O2)O[C@@H]3c4cc5c(cc4[C@H]([C@@H]6[C@@H]3COC6=O)c7cc(c(c(c7)OC)O)OC)OCO5)O)O
  • InChI=1S/C29H32O13/c1-11-36-9-20-27(40-11)24(31)25(32)29(41-20)42-26-14-7-17-16(38-10-39-17)6-13(14)21(22-15(26)8-37-28(22)33)12-4-18(34-2)23(30)19(5-12)35-3/h4-7,11,15,20-22,24-27,29-32H,8-10H2,1-3H3/t11-,15+,20-,21-,22+,24-,25-,26-,27-,29+/m1/s1 checkY
  • Key:VJJPUSNTGOMMGY-MRVIYFEKSA-N checkY
  

Etoposide, sold under the brand name Vepesid among others, is a chemotherapy medication used for the treatments of a number of types of cancer including testicular cancer, lung cancer, lymphoma, leukemia, neuroblastoma, and ovarian cancer.[1] It is also used for hemophagocytic lymphohistiocytosis.[2] It is used by mouth or injection into a vein.[1]

Side effects are very common.[1] They can include low blood cell counts, vomiting, loss of appetite, diarrhea, hair loss, and fever.[1] Other severe side effects include allergic reactions and low blood pressure.[1][3] Use during pregnancy will likely harm the baby.[1] Etoposide is in the topoisomerase inhibitor family of medication.[1] It is believed to work by damaging DNA.[1]

Etoposide was approved for medical use in the United States in 1983.[1] It is on the World Health Organization's List of Essential Medicines.[4]

Medical uses[]

Etoposide is used as a form of chemotherapy for cancers such as Kaposi’s sarcoma, Ewing's sarcoma, lung cancer, testicular cancer, lymphoma, nonlymphocytic leukemia, and glioblastoma multiforme. It is often given in combination with other drugs (such as bleomycin in treating testicular cancer). It is also sometimes used in a conditioning regimen prior to a bone marrow or blood stem cell transplant.[5]

Administration[]

It is given intravenously (IV) or orally in capsule or tablet form. If the drug is given IV, it must be done slowly over a 30- to 60-minute period because it can lower blood pressure as it is being administered. Blood pressure is checked often during infusing, with the speed of administration adjusted accordingly.

Side effects[]

Common are:

  • infusion site reactions
  • low blood pressure
  • hair loss
  • pain and or burning at the IV site
  • constipation or diarrhea
  • metallic food taste
  • bone marrow suppression, leading to:
    • decreased white blood cell counts (leading to increased susceptibility to infections)
    • low red blood cell counts (anemia)
    • low platelet counts (leading to easy bruising and bleeding)

Less common are:

  • nausea and vomiting
  • allergic-type reactions
  • rash
  • fever, often occurring shortly after IV administration and not due to infection
  • mouth sores
  • acute myeloid leukemia (which can be treated with etoposide itself)

When given with warfarin, it may cause bleeding.[6]

Pharmacology[]

Mechanism of action[]

Etoposide forms a ternary complex with DNA and the topoisomerase II enzyme, which is an enzyme that aids in relaxing negative or positive supercoils in DNA. Topoisomerase II normally will form a double-stranded break in one DNA double-strand, allow another to pass through, and re-ligate the broken strands. Etoposide's binding prevents topoisomerase II from re-ligating the broken DNA strands, which causes the DNA breaks made by topoisomerase II to stay broken, and also prevents the topoisomerase II molecule from leaving the site and relieving tension elsewhere. This results in a double-strand break in the DNA that can have various deleterious effects on the cell, and depletion of topoisomerase II available to relieve further tension.[7] Cancer cells rely on this enzyme more than healthy cells, since they divide more rapidly. Therefore, this causes errors in DNA synthesis and promotes apoptosis of the cancer cell.[5][8]

Chemistry[]

An illustration of the wild mandrake, showing part of the rhizome (at bottom)

Etoposide is a semisynthetic derivative of podophyllotoxin from the rhizome of the wild mandrake (Podophyllum peltatum). More specifically, it is a glycoside of podophyllotoxin with a D-glucose derivative. It is chemically similar to the anti-cancer drug teniposide, being distinguished only by a methyl group where teniposide has a thienyl.[9] Both these compounds have been developed with the aim of creating less toxic derivatives of podophyllotoxin.[10]

The substance is a white to yellow-brown, crystalline powder. It is soluble in organic solvents.[10]

It is used in form of its salt etoposide phosphate.

History[]

Etoposide was first synthesized in 1966 and U.S. Food and Drug Administration approval was granted in 1983.[5]

The nickname VP-16 likely comes from a compounding of the last name of one of the chemists who performed early work on the drug (von Wartburg) and podophyllotoxin.[11] Another scientist who was integral in the development of podophyllotoxin-based chemotherapeutics was the medical pharmacologist Hartmann F. Stähelin.

References[]

  1. ^ a b c d e f g h i "Etoposide". The American Society of Health-System Pharmacists. Archived from the original on 31 March 2016. Retrieved 8 December 2016.
  2. ^ Yildiz, H.; Van Den Neste, E.; Defour, J. P.; Danse, E.; Yombi, J. C. (2020). "Adult haemophagocytic lymphohistiocytosis: A Review". QJM: Monthly Journal of the Association of Physicians. doi:10.1093/qjmed/hcaa011. PMID 31943120.
  3. ^ World Health Organization (2009). Stuart MC, Kouimtzi M, Hill SR (eds.). WHO Model Formulary 2008. World Health Organization. p. 227. hdl:10665/44053. ISBN 9789241547659.
  4. ^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  5. ^ a b c Hande KR (1998). "Etoposide: four decades of development of a topoisomerase II inhibitor". Eur. J. Cancer. 34 (10): 1514–21. doi:10.1016/S0959-8049(98)00228-7. PMID 9893622.
  6. ^ Longe JL (2002). Gale Encyclopedia Of Cancer: A Guide To Cancer And Its Treatments. Detroit: Thomson Gale. pp. 397–399. ISBN 978-1-4144-0362-5.
  7. ^ Pommier Y, Leo E, Zhang H, Marchand C (2010). "DNA topoisomerases and their poisoning by anticancer and antibacterial drugs". Chem. Biol. 17 (5): 421–33. doi:10.1016/j.chembiol.2010.04.012. PMC 7316379. PMID 20534341.
  8. ^ Gordaliza M, García PA, del Corral JM, Castro MA, Gómez-Zurita MA (2004). "Podophyllotoxin: distribution, sources, applications and new cytotoxic derivatives". Toxicon. 44 (4): 441–59. doi:10.1016/j.toxicon.2004.05.008. PMID 15302526.
  9. ^ Mutschler, Ernst; Schäfer-Korting, Monika (2001). Arzneimittelwirkungen (in German) (8 ed.). Stuttgart: Wissenschaftliche Verlagsgesellschaft. pp. 894–5. ISBN 3-8047-1763-2.
  10. ^ a b Dinnendahl, V; Fricke, U, eds. (2015). Arzneistoff-Profile (in German). Vol. 4 (28 ed.). Eschborn, Germany: Govi Pharmazeutischer Verlag. ISBN 978-3-7741-9846-3.
  11. ^ Kuhn M, Von Wartburg A (1967). "Podophyllum-Lignane: Struktur und Absolutkonfiguration von Podorhizol-β-D-glucosid ( = Lignan F). 19. Mitt. über mitosehemmende Naturstoffe [1]". Helvetica Chimica Acta. 50 (6): 1546–65. doi:10.1002/hlca.19670500614. Archived from the original on 2013-01-05.

External links[]

  • "Etoposide". Drug Information Portal. U.S. National Library of Medicine.
  • "Etoposide phosphate". Drug Information Portal. U.S. National Library of Medicine.
  • "Etoposide". National Cancer Institute. 12 August 2008.
  • "Etoposide". NCI Drug Dictionary. National Cancer Institute.
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