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Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges
Liquid biopsy has been established as a powerful, minimally invasive, tool to detect clinically actionable aberrations across numerous cancer types in real-time. With the development of new therapeutic agents in prostate cancer (PC) including DNA repair targeted therapies, this is especially attract...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553885/ https://www.ncbi.nlm.nih.gov/pubmed/35715640 http://dx.doi.org/10.1038/s41416-022-01881-9 |
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author | Trujillo, Blanca Wu, Anjui Wetterskog, Daniel Attard, Gerhardt |
author_facet | Trujillo, Blanca Wu, Anjui Wetterskog, Daniel Attard, Gerhardt |
author_sort | Trujillo, Blanca |
collection | PubMed |
description | Liquid biopsy has been established as a powerful, minimally invasive, tool to detect clinically actionable aberrations across numerous cancer types in real-time. With the development of new therapeutic agents in prostate cancer (PC) including DNA repair targeted therapies, this is especially attractive. However, there is unclarity on how best to screen for PC, improve risk stratification and ultimately how to treat advanced disease. Therefore, there is an urgent need to develop better biomarkers to help guide oncologists’ decisions in these settings. Circulating tumour cells (CTCs), exosomes and cell-free DNA/RNA (cfDNA/cfRNA) analysis, including epigenetic features such as methylation, have all shown potential in prognostication, treatment response assessment and detection of emerging mechanisms of resistance. However, there are still challenges to overcome prior to implementing liquid biopsies in routine clinical practice such as preanalytical considerations including blood collection and storage, the cost of CTC isolation and enrichment, low-circulating tumour content as a limitation for genomic analysis and how to better interpret the sequencing data generated. In this review, we describe an overview of the up-to-date clinical opportunities in the management of PC through blood-based liquid biopsies and the next steps for its implementation in personalised treatment guidance. |
format | Online Article Text |
id | pubmed-9553885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95538852022-10-13 Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges Trujillo, Blanca Wu, Anjui Wetterskog, Daniel Attard, Gerhardt Br J Cancer Review Article Liquid biopsy has been established as a powerful, minimally invasive, tool to detect clinically actionable aberrations across numerous cancer types in real-time. With the development of new therapeutic agents in prostate cancer (PC) including DNA repair targeted therapies, this is especially attractive. However, there is unclarity on how best to screen for PC, improve risk stratification and ultimately how to treat advanced disease. Therefore, there is an urgent need to develop better biomarkers to help guide oncologists’ decisions in these settings. Circulating tumour cells (CTCs), exosomes and cell-free DNA/RNA (cfDNA/cfRNA) analysis, including epigenetic features such as methylation, have all shown potential in prognostication, treatment response assessment and detection of emerging mechanisms of resistance. However, there are still challenges to overcome prior to implementing liquid biopsies in routine clinical practice such as preanalytical considerations including blood collection and storage, the cost of CTC isolation and enrichment, low-circulating tumour content as a limitation for genomic analysis and how to better interpret the sequencing data generated. In this review, we describe an overview of the up-to-date clinical opportunities in the management of PC through blood-based liquid biopsies and the next steps for its implementation in personalised treatment guidance. Nature Publishing Group UK 2022-06-17 2022-11-01 /pmc/articles/PMC9553885/ /pubmed/35715640 http://dx.doi.org/10.1038/s41416-022-01881-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Trujillo, Blanca Wu, Anjui Wetterskog, Daniel Attard, Gerhardt Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title | Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title_full | Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title_fullStr | Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title_full_unstemmed | Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title_short | Blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
title_sort | blood-based liquid biopsies for prostate cancer: clinical opportunities and challenges |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9553885/ https://www.ncbi.nlm.nih.gov/pubmed/35715640 http://dx.doi.org/10.1038/s41416-022-01881-9 |
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