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Emerging Biomarker-Guided Therapies in Prostate Cancer

Prostate cancer remains one of the leading causes of cancer death in men worldwide. In the past decade, several new treatments for advanced prostate cancer have been approved. With a wide variety of available drugs, including cytotoxic agents, androgen receptor axis-targeted therapies, and alpha-emi...

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Autores principales: Deluce, Jasna E., Cardenas, Luisa, Lalani, Aly-Khan, Maleki Vareki, Saman, Fernandes, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319825/
https://www.ncbi.nlm.nih.gov/pubmed/35877260
http://dx.doi.org/10.3390/curroncol29070400
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author Deluce, Jasna E.
Cardenas, Luisa
Lalani, Aly-Khan
Maleki Vareki, Saman
Fernandes, Ricardo
author_facet Deluce, Jasna E.
Cardenas, Luisa
Lalani, Aly-Khan
Maleki Vareki, Saman
Fernandes, Ricardo
author_sort Deluce, Jasna E.
collection PubMed
description Prostate cancer remains one of the leading causes of cancer death in men worldwide. In the past decade, several new treatments for advanced prostate cancer have been approved. With a wide variety of available drugs, including cytotoxic agents, androgen receptor axis-targeted therapies, and alpha-emitting radiation therapy, identifying their optimal sequencing remains a challenge. Progress in the understanding of the biology of prostate cancer has provided an opportunity for a more refined and personalized treatment selection process. With the advancement of molecular sequencing techniques, genomic precision through the identification of potential treatment targets and predictive biomarkers has been rapidly evolving. In this review, we discussed biomarker-driven treatments for advanced prostate cancer. First, we presented predictive biomarkers for established, global standard treatments for advanced diseases, such as chemotherapy and androgen receptor axis-targeted agents. We also discussed targeted agents with recent approval for special populations, such as poly ADP ribose polymerase (PARP) inhibitors in patients with metastatic castrate-resistant prostate cancer with homologous recombination repair-deficient tumors, pembrolizumab in patients with high levels of microsatellite instability or high tumor mutational burden, and prostate-specific membrane antigen (PSMA) directed radioligand theragnostic treatment for PSMA expressing tumors. Additionally, we discussed evolving treatments, such as cancer vaccines, chimeric antigen receptor T-cells (CAR-T), Bispecific T-cell engagers (BiTEs), other targeted agents such as AKT inhibitors, and various combination treatments. In summary, advances in molecular genetics have begun to propel personalized medicine forward in the management of advanced prostate cancer, allowing for a more precise, biomarker-driven treatment selection with the goal of improving overall efficacy.
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spelling pubmed-93198252022-07-27 Emerging Biomarker-Guided Therapies in Prostate Cancer Deluce, Jasna E. Cardenas, Luisa Lalani, Aly-Khan Maleki Vareki, Saman Fernandes, Ricardo Curr Oncol Review Prostate cancer remains one of the leading causes of cancer death in men worldwide. In the past decade, several new treatments for advanced prostate cancer have been approved. With a wide variety of available drugs, including cytotoxic agents, androgen receptor axis-targeted therapies, and alpha-emitting radiation therapy, identifying their optimal sequencing remains a challenge. Progress in the understanding of the biology of prostate cancer has provided an opportunity for a more refined and personalized treatment selection process. With the advancement of molecular sequencing techniques, genomic precision through the identification of potential treatment targets and predictive biomarkers has been rapidly evolving. In this review, we discussed biomarker-driven treatments for advanced prostate cancer. First, we presented predictive biomarkers for established, global standard treatments for advanced diseases, such as chemotherapy and androgen receptor axis-targeted agents. We also discussed targeted agents with recent approval for special populations, such as poly ADP ribose polymerase (PARP) inhibitors in patients with metastatic castrate-resistant prostate cancer with homologous recombination repair-deficient tumors, pembrolizumab in patients with high levels of microsatellite instability or high tumor mutational burden, and prostate-specific membrane antigen (PSMA) directed radioligand theragnostic treatment for PSMA expressing tumors. Additionally, we discussed evolving treatments, such as cancer vaccines, chimeric antigen receptor T-cells (CAR-T), Bispecific T-cell engagers (BiTEs), other targeted agents such as AKT inhibitors, and various combination treatments. In summary, advances in molecular genetics have begun to propel personalized medicine forward in the management of advanced prostate cancer, allowing for a more precise, biomarker-driven treatment selection with the goal of improving overall efficacy. MDPI 2022-07-18 /pmc/articles/PMC9319825/ /pubmed/35877260 http://dx.doi.org/10.3390/curroncol29070400 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Deluce, Jasna E.
Cardenas, Luisa
Lalani, Aly-Khan
Maleki Vareki, Saman
Fernandes, Ricardo
Emerging Biomarker-Guided Therapies in Prostate Cancer
title Emerging Biomarker-Guided Therapies in Prostate Cancer
title_full Emerging Biomarker-Guided Therapies in Prostate Cancer
title_fullStr Emerging Biomarker-Guided Therapies in Prostate Cancer
title_full_unstemmed Emerging Biomarker-Guided Therapies in Prostate Cancer
title_short Emerging Biomarker-Guided Therapies in Prostate Cancer
title_sort emerging biomarker-guided therapies in prostate cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319825/
https://www.ncbi.nlm.nih.gov/pubmed/35877260
http://dx.doi.org/10.3390/curroncol29070400
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