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Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer

Significant progress has been made in the understanding of the underlying cancer biology of castration‐resistant prostate cancer (CRPC) with the androgen receptor (AR) signalling pathway remaining implicated throughout the prostate cancer disease continuum. Reactivation of the AR signalling pathway...

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Detalles Bibliográficos
Autores principales: Schalken, Jack, Fitzpatrick, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744713/
https://www.ncbi.nlm.nih.gov/pubmed/25818596
http://dx.doi.org/10.1111/bju.13123
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author Schalken, Jack
Fitzpatrick, John M.
author_facet Schalken, Jack
Fitzpatrick, John M.
author_sort Schalken, Jack
collection PubMed
description Significant progress has been made in the understanding of the underlying cancer biology of castration‐resistant prostate cancer (CRPC) with the androgen receptor (AR) signalling pathway remaining implicated throughout the prostate cancer disease continuum. Reactivation of the AR signalling pathway is considered to be a key driver of CRPC progression and, as such, the AR is a logical target for therapy in CRPC. The objective of this review was to understand the importance of AR signalling in the treatment of patients with metastatic CRPC (mCRPC) and to discuss the clinical benefits associated with inhibition of the AR signalling pathway. A search was conducted to identify articles relating to the role of AR signalling in CRPC and therapies that inhibit the AR signalling pathway. Current understanding of prostate cancer has identified the AR signalling pathway as a logical target for the treatment of CRPC. Available therapies that inhibit the AR signalling pathway include AR blockers, androgen biosynthesis inhibitors, and AR signalling inhibitors. Enzalutamide, the first approved AR signalling inhibitor, has a novel mode of action targeting AR signalling at three key stages. The direct mode of action of enzalutamide has been shown to translate into clinical responses in patients with mCRPC. In conclusion, the targeting of the AR signalling pathway in patients with mCRPC results in numerous clinical benefits. As the number of treatment options increase, more trials evaluating the sequencing and combination of treatments are required. This review highlights the continued importance of targeting a key driver in the progression of CRPC, AR signalling, and the clinical benefits associated with inhibition of the AR signalling pathway in the treatment of patients with CRPC.
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spelling pubmed-47447132016-02-18 Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer Schalken, Jack Fitzpatrick, John M. BJU Int Review Significant progress has been made in the understanding of the underlying cancer biology of castration‐resistant prostate cancer (CRPC) with the androgen receptor (AR) signalling pathway remaining implicated throughout the prostate cancer disease continuum. Reactivation of the AR signalling pathway is considered to be a key driver of CRPC progression and, as such, the AR is a logical target for therapy in CRPC. The objective of this review was to understand the importance of AR signalling in the treatment of patients with metastatic CRPC (mCRPC) and to discuss the clinical benefits associated with inhibition of the AR signalling pathway. A search was conducted to identify articles relating to the role of AR signalling in CRPC and therapies that inhibit the AR signalling pathway. Current understanding of prostate cancer has identified the AR signalling pathway as a logical target for the treatment of CRPC. Available therapies that inhibit the AR signalling pathway include AR blockers, androgen biosynthesis inhibitors, and AR signalling inhibitors. Enzalutamide, the first approved AR signalling inhibitor, has a novel mode of action targeting AR signalling at three key stages. The direct mode of action of enzalutamide has been shown to translate into clinical responses in patients with mCRPC. In conclusion, the targeting of the AR signalling pathway in patients with mCRPC results in numerous clinical benefits. As the number of treatment options increase, more trials evaluating the sequencing and combination of treatments are required. This review highlights the continued importance of targeting a key driver in the progression of CRPC, AR signalling, and the clinical benefits associated with inhibition of the AR signalling pathway in the treatment of patients with CRPC. John Wiley and Sons Inc. 2015-06-06 2016-02 /pmc/articles/PMC4744713/ /pubmed/25818596 http://dx.doi.org/10.1111/bju.13123 Text en © 2015 The Authors BJU International published by John Wiley & Sons Ltd on behalf of BJU International. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Schalken, Jack
Fitzpatrick, John M.
Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title_full Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title_fullStr Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title_full_unstemmed Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title_short Enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
title_sort enzalutamide: targeting the androgen signalling pathway in metastatic castration‐resistant prostate cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744713/
https://www.ncbi.nlm.nih.gov/pubmed/25818596
http://dx.doi.org/10.1111/bju.13123
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