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Urinary biomarkers for the detection of ovarian cancer: a systematic review

Currently, the only definitive method for diagnosing ovarian cancer involves histological examination of tissue obtained at time of surgery or by invasive biopsy. Blood has traditionally been the biofluid of choice in ovarian cancer biomarker discovery; however, there has been a growing interest in...

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Autores principales: Owens, Gemma L, Barr, Chloe E, White, Holly, Njoku, Kelechi, Crosbie, Emma J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118979/
https://www.ncbi.nlm.nih.gov/pubmed/35166350
http://dx.doi.org/10.1093/carcin/bgac016
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author Owens, Gemma L
Barr, Chloe E
White, Holly
Njoku, Kelechi
Crosbie, Emma J
author_facet Owens, Gemma L
Barr, Chloe E
White, Holly
Njoku, Kelechi
Crosbie, Emma J
author_sort Owens, Gemma L
collection PubMed
description Currently, the only definitive method for diagnosing ovarian cancer involves histological examination of tissue obtained at time of surgery or by invasive biopsy. Blood has traditionally been the biofluid of choice in ovarian cancer biomarker discovery; however, there has been a growing interest in exploring urinary biomarkers, particularly as it is non-invasive. In this systematic review, we present the diagnostic accuracy of urinary biomarker candidates for the detection of ovarian cancer. A comprehensive literature search was performed using the MEDLINE/PubMed and EMBASE, up to 1 April 2021. All included studies reported the diagnostic accuracy using sensitivity and/or specificity and/or receiver operating characteristics (ROC) curve. Risk of bias and applicability of included studies were assessed using the QUADAS-2 tool. Twenty-seven studies were included in the narrative synthesis. Protein/peptide biomarkers were most commonly described (n = 18), with seven studies reporting composite scores of multiple protein-based targets. The most frequently described urinary protein biomarker was HE4 (n = 5), with three studies reporting a sensitivity and specificity > 80%. Epigenetic (n = 1) and metabolomic/organic compound biomarkers (n = 8) were less commonly described. Overall, six studies achieved a sensitivity and specificity of >90% and/or an AUC > 0.9. Evaluation of urinary biomarkers for the detection of ovarian cancer is a dynamic and growing field. Currently, the most promising biomarkers are those that interrogate metabolomic pathways and organic compounds, or quantify multiple proteins. Such biomarkers require external validation in large, prospective observational studies before they can be implemented into clinical practice.
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spelling pubmed-91189792022-05-20 Urinary biomarkers for the detection of ovarian cancer: a systematic review Owens, Gemma L Barr, Chloe E White, Holly Njoku, Kelechi Crosbie, Emma J Carcinogenesis Cancer Biomarkers and Molecular Epidemiology Currently, the only definitive method for diagnosing ovarian cancer involves histological examination of tissue obtained at time of surgery or by invasive biopsy. Blood has traditionally been the biofluid of choice in ovarian cancer biomarker discovery; however, there has been a growing interest in exploring urinary biomarkers, particularly as it is non-invasive. In this systematic review, we present the diagnostic accuracy of urinary biomarker candidates for the detection of ovarian cancer. A comprehensive literature search was performed using the MEDLINE/PubMed and EMBASE, up to 1 April 2021. All included studies reported the diagnostic accuracy using sensitivity and/or specificity and/or receiver operating characteristics (ROC) curve. Risk of bias and applicability of included studies were assessed using the QUADAS-2 tool. Twenty-seven studies were included in the narrative synthesis. Protein/peptide biomarkers were most commonly described (n = 18), with seven studies reporting composite scores of multiple protein-based targets. The most frequently described urinary protein biomarker was HE4 (n = 5), with three studies reporting a sensitivity and specificity > 80%. Epigenetic (n = 1) and metabolomic/organic compound biomarkers (n = 8) were less commonly described. Overall, six studies achieved a sensitivity and specificity of >90% and/or an AUC > 0.9. Evaluation of urinary biomarkers for the detection of ovarian cancer is a dynamic and growing field. Currently, the most promising biomarkers are those that interrogate metabolomic pathways and organic compounds, or quantify multiple proteins. Such biomarkers require external validation in large, prospective observational studies before they can be implemented into clinical practice. Oxford University Press 2022-02-15 /pmc/articles/PMC9118979/ /pubmed/35166350 http://dx.doi.org/10.1093/carcin/bgac016 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Biomarkers and Molecular Epidemiology
Owens, Gemma L
Barr, Chloe E
White, Holly
Njoku, Kelechi
Crosbie, Emma J
Urinary biomarkers for the detection of ovarian cancer: a systematic review
title Urinary biomarkers for the detection of ovarian cancer: a systematic review
title_full Urinary biomarkers for the detection of ovarian cancer: a systematic review
title_fullStr Urinary biomarkers for the detection of ovarian cancer: a systematic review
title_full_unstemmed Urinary biomarkers for the detection of ovarian cancer: a systematic review
title_short Urinary biomarkers for the detection of ovarian cancer: a systematic review
title_sort urinary biomarkers for the detection of ovarian cancer: a systematic review
topic Cancer Biomarkers and Molecular Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9118979/
https://www.ncbi.nlm.nih.gov/pubmed/35166350
http://dx.doi.org/10.1093/carcin/bgac016
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