Difference between revisions of "Enzalutamide (Xtandi)"

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==References==
 
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[[Category:Drugs FDA approved in 2012]]

Revision as of 05:37, 15 October 2012

FDA approved 8/31/2012. Also known as MDV3100.

General information

Class/mechanism: Antiandrogen; androgen receptor inhibitor (ARI) or androgen receptor signaling inhibitor (ARSI). Enzalutamide competitively inhibits testosterone from binding to the androgen receptor, interferes with translocation of the androgen receptor to the nucleus, and inhibits binding to DNA, resulting in decreased prostate cancer proliferation and cell death.[1][2][3]
Route: PO
Extravasation: n/a

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.

Diseases for which it is used

Clinical trials

Patient drug information

References

  1. 1.0 1.1 Enzalutamide (Xtandi) package insert
  2. Enzalutamide (Xtandi) package insert (locally hosted backup)
  3. Enzalutamide (MDV3100) manufacturer's website
  4. Scher HI, Fizazi K, Saad F, Taplin ME, Sternberg CN, Miller MD, de Wit R, Mulders P, Chi KN, Shore ND, Armstrong AJ, Flaig TW, Fléchon A, Mainwaring P, Fleming M, Hainsworth JD, Hirmand M, Selby B, Seely L, de Bono JS; the AFFIRM Investigators. Increased Survival with Enzalutamide in Prostate Cancer after Chemotherapy. N Engl J Med. 2012 Aug 15. [Epub ahead of print] link to original article contains verified protocol PubMed ClinicalTrials.gov