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The path forward in prostate cancer therapeutics

The last decade has seen remarkable advances in the treatment of prostate cancer. Until 2010, only docetaxel had demonstrated the ability to improve the survival in metastatic castration-resistant prostate cancer (mCRPC).1 While effective, many men were reluctant to get treatment with docetaxel beca...

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Autores principales: Aragon-Ching, Jeanny B, Madan, Ravi A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952473/
https://www.ncbi.nlm.nih.gov/pubmed/29536949
http://dx.doi.org/10.4103/aja.aja_3_18
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author Aragon-Ching, Jeanny B
Madan, Ravi A
author_facet Aragon-Ching, Jeanny B
Madan, Ravi A
author_sort Aragon-Ching, Jeanny B
collection PubMed
description The last decade has seen remarkable advances in the treatment of prostate cancer. Until 2010, only docetaxel had demonstrated the ability to improve the survival in metastatic castration-resistant prostate cancer (mCRPC).1 While effective, many men were reluctant to get treatment with docetaxel because of the perceived toxicity, thereby further limiting the benefit of the one available and effective therapy. Remarkably, within the last 8 years, the field has seen a multitude of therapies that demonstrate an ability to extend survival for men with prostate cancer. Abiraterone and enzalutamide demonstrated the importance of the androgen axis in propelling prostate cancer growth.23 Sipuleucel-T was immunotherapy's entry into the evolving prostate cancer armamentarium, as the therapeutic cancer vaccine established an ability to extend survival despite an apparent lack of short-term effect on progression-free survival and prostate-specific antigen (PSA).4 Radium-223 built on the palliative success of previous radiopharmaceuticals, but this alpha-emitting agent importantly had limited hematologic-related toxicity and was associated with a survival advantage, unlike its in-class predecessors.5 Cabazitaxel also emerged as a second-line chemotherapy option in patients who had already progressed on docetaxel.6
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spelling pubmed-59524732018-06-01 The path forward in prostate cancer therapeutics Aragon-Ching, Jeanny B Madan, Ravi A Asian J Androl Invited Editorial The last decade has seen remarkable advances in the treatment of prostate cancer. Until 2010, only docetaxel had demonstrated the ability to improve the survival in metastatic castration-resistant prostate cancer (mCRPC).1 While effective, many men were reluctant to get treatment with docetaxel because of the perceived toxicity, thereby further limiting the benefit of the one available and effective therapy. Remarkably, within the last 8 years, the field has seen a multitude of therapies that demonstrate an ability to extend survival for men with prostate cancer. Abiraterone and enzalutamide demonstrated the importance of the androgen axis in propelling prostate cancer growth.23 Sipuleucel-T was immunotherapy's entry into the evolving prostate cancer armamentarium, as the therapeutic cancer vaccine established an ability to extend survival despite an apparent lack of short-term effect on progression-free survival and prostate-specific antigen (PSA).4 Radium-223 built on the palliative success of previous radiopharmaceuticals, but this alpha-emitting agent importantly had limited hematologic-related toxicity and was associated with a survival advantage, unlike its in-class predecessors.5 Cabazitaxel also emerged as a second-line chemotherapy option in patients who had already progressed on docetaxel.6 Medknow Publications & Media Pvt Ltd 2018 2018-03-09 /pmc/articles/PMC5952473/ /pubmed/29536949 http://dx.doi.org/10.4103/aja.aja_3_18 Text en Copyright: © The Author(s)(2018) http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Invited Editorial
Aragon-Ching, Jeanny B
Madan, Ravi A
The path forward in prostate cancer therapeutics
title The path forward in prostate cancer therapeutics
title_full The path forward in prostate cancer therapeutics
title_fullStr The path forward in prostate cancer therapeutics
title_full_unstemmed The path forward in prostate cancer therapeutics
title_short The path forward in prostate cancer therapeutics
title_sort path forward in prostate cancer therapeutics
topic Invited Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952473/
https://www.ncbi.nlm.nih.gov/pubmed/29536949
http://dx.doi.org/10.4103/aja.aja_3_18
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