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Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics

PURPOSE: Prostate cancer (PCa) is the second most common cancer in men. The urge to guide treatment tactics based on personal clinical risk factors has evolved in the era of human genome sequencing. To date, personalized approaches to managing PCa patients have not yet been developed. Radiogenomics...

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Autores principales: Mytsyk, Yulian, Borzhiyevs’kyy, Andriy, Kobilnyk, Yuriy, Shulyak, A.V., Dutka, Ihor, Borzhiyevs’kyy, Oleksandr, Górecki, Andrzej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8814894/
https://www.ncbi.nlm.nih.gov/pubmed/35140829
http://dx.doi.org/10.5114/pjr.2022.113204
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author Mytsyk, Yulian
Borzhiyevs’kyy, Andriy
Kobilnyk, Yuriy
Shulyak, A.V.
Dutka, Ihor
Borzhiyevs’kyy, Oleksandr
Górecki, Andrzej
author_facet Mytsyk, Yulian
Borzhiyevs’kyy, Andriy
Kobilnyk, Yuriy
Shulyak, A.V.
Dutka, Ihor
Borzhiyevs’kyy, Oleksandr
Górecki, Andrzej
author_sort Mytsyk, Yulian
collection PubMed
description PURPOSE: Prostate cancer (PCa) is the second most common cancer in men. The urge to guide treatment tactics based on personal clinical risk factors has evolved in the era of human genome sequencing. To date, personalized approaches to managing PCa patients have not yet been developed. Radiogenomics is a relatively new term, used to refer to the study of genetic variation associated with imaging features of the tumour in order to improve the prognostication of the disease course. MATERIAL AND METHODS: The study is a review of recent knowledge regarding potential clinical applications of radiogenomics in personalized treatment of PCa. RESULTS: Recent investigations have proven that by combining data on individual genetic tumour features, and radiomic profiling (radiologic-molecular correlation), with traditional staging procedures in order to personalize treatment of PCa, an improved prognostication of PCa course can be performed, and overtreatment of indolent cancer can be avoided. It was found that a combination of multiparametric MRI and gene expression data allowed the detection of radiomic features of PCa, which correlated with a number of gene signatures associated with adverse outcomes. It was revealed that several molecular markers may drive tumour upstaging, allowed the distinction between the PCa stages, and correlated with aggressiveness-related radiomic features. CONCLUSIONS: The radiogenomics of PCa is not a comprehensively investigated area of oncourology. The combination of genomics and radiomics as integrative parts of precision medicine in the future has the potential to become the foundation for a personalized approach to the management of PCa.
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spelling pubmed-88148942022-02-08 Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics Mytsyk, Yulian Borzhiyevs’kyy, Andriy Kobilnyk, Yuriy Shulyak, A.V. Dutka, Ihor Borzhiyevs’kyy, Oleksandr Górecki, Andrzej Pol J Radiol Review Paper PURPOSE: Prostate cancer (PCa) is the second most common cancer in men. The urge to guide treatment tactics based on personal clinical risk factors has evolved in the era of human genome sequencing. To date, personalized approaches to managing PCa patients have not yet been developed. Radiogenomics is a relatively new term, used to refer to the study of genetic variation associated with imaging features of the tumour in order to improve the prognostication of the disease course. MATERIAL AND METHODS: The study is a review of recent knowledge regarding potential clinical applications of radiogenomics in personalized treatment of PCa. RESULTS: Recent investigations have proven that by combining data on individual genetic tumour features, and radiomic profiling (radiologic-molecular correlation), with traditional staging procedures in order to personalize treatment of PCa, an improved prognostication of PCa course can be performed, and overtreatment of indolent cancer can be avoided. It was found that a combination of multiparametric MRI and gene expression data allowed the detection of radiomic features of PCa, which correlated with a number of gene signatures associated with adverse outcomes. It was revealed that several molecular markers may drive tumour upstaging, allowed the distinction between the PCa stages, and correlated with aggressiveness-related radiomic features. CONCLUSIONS: The radiogenomics of PCa is not a comprehensively investigated area of oncourology. The combination of genomics and radiomics as integrative parts of precision medicine in the future has the potential to become the foundation for a personalized approach to the management of PCa. Termedia Publishing House 2022-01-26 /pmc/articles/PMC8814894/ /pubmed/35140829 http://dx.doi.org/10.5114/pjr.2022.113204 Text en © Pol J Radiol 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0). License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review Paper
Mytsyk, Yulian
Borzhiyevs’kyy, Andriy
Kobilnyk, Yuriy
Shulyak, A.V.
Dutka, Ihor
Borzhiyevs’kyy, Oleksandr
Górecki, Andrzej
Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title_full Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title_fullStr Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title_full_unstemmed Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title_short Personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
title_sort personalized management of prostate cancer: from molecular and imaging markers to radiogenomics
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8814894/
https://www.ncbi.nlm.nih.gov/pubmed/35140829
http://dx.doi.org/10.5114/pjr.2022.113204
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