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Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date
Advances in therapies have led to the approval of six therapeutic agents since 2004, each demonstrating overall survival benefit in randomized studies, and these have significantly improved the outlook for men facing metastatic castration-resistant prostate cancer (CRPC). More recently, efforts have...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905496/ https://www.ncbi.nlm.nih.gov/pubmed/29695920 http://dx.doi.org/10.2147/OTT.S147168 |
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author | Chong, Julio T Oh, William K Liaw, Bobby C |
author_facet | Chong, Julio T Oh, William K Liaw, Bobby C |
author_sort | Chong, Julio T |
collection | PubMed |
description | Advances in therapies have led to the approval of six therapeutic agents since 2004, each demonstrating overall survival benefit in randomized studies, and these have significantly improved the outlook for men facing metastatic castration-resistant prostate cancer (CRPC). More recently, efforts have been directed at trying to effect change at earlier phases of the disease. Apalutamide (ARN-509), a second-generation androgen receptor antagonist, recently received approval in the nonmetastatic (M0) CRPC space. Similar to enzalutamide, apalutamide inhibits the binding of androgen to androgen receptor (AR), nuclear translocation of the androgen–AR complex, and binding of AR transcription complex to DNA-binding sites and transcription elements. Phase I and II trial experience demonstrates the safety and tolerability of apalutamide, as well as its efficacy in effecting prostate-specific antigen response and radiographic-free survival in CRPC. US Food and Drug Administration approval in M0 CRPC was granted following positive results from the phase III SPARTAN study, where apalutamide demonstrated significant improvements in metastasis-free survival and time to symptomatic progression as compared to placebo. |
format | Online Article Text |
id | pubmed-5905496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59054962018-04-25 Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date Chong, Julio T Oh, William K Liaw, Bobby C Onco Targets Ther Review Advances in therapies have led to the approval of six therapeutic agents since 2004, each demonstrating overall survival benefit in randomized studies, and these have significantly improved the outlook for men facing metastatic castration-resistant prostate cancer (CRPC). More recently, efforts have been directed at trying to effect change at earlier phases of the disease. Apalutamide (ARN-509), a second-generation androgen receptor antagonist, recently received approval in the nonmetastatic (M0) CRPC space. Similar to enzalutamide, apalutamide inhibits the binding of androgen to androgen receptor (AR), nuclear translocation of the androgen–AR complex, and binding of AR transcription complex to DNA-binding sites and transcription elements. Phase I and II trial experience demonstrates the safety and tolerability of apalutamide, as well as its efficacy in effecting prostate-specific antigen response and radiographic-free survival in CRPC. US Food and Drug Administration approval in M0 CRPC was granted following positive results from the phase III SPARTAN study, where apalutamide demonstrated significant improvements in metastasis-free survival and time to symptomatic progression as compared to placebo. Dove Medical Press 2018-04-12 /pmc/articles/PMC5905496/ /pubmed/29695920 http://dx.doi.org/10.2147/OTT.S147168 Text en © 2018 Chong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Chong, Julio T Oh, William K Liaw, Bobby C Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title | Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title_full | Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title_fullStr | Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title_full_unstemmed | Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title_short | Profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
title_sort | profile of apalutamide in the treatment of metastatic castration-resistant prostate cancer: evidence to date |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5905496/ https://www.ncbi.nlm.nih.gov/pubmed/29695920 http://dx.doi.org/10.2147/OTT.S147168 |
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