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Narrative review of developing new biomarkers for decision making in advanced testis cancer

Management of testicular germ cell tumor (GCT) patients is based on clinical determinants, mainly CT scan and serum tumor markers (alpha-fetoprotein, beta subunit of HCG and LDH). Treatment decisions are usually straightforward for patients with clear evidence of metastatic disease, confirmed either...

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Autores principales: Nappi, Lucia, Nichols, Craig, Kollmannsberger, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575592/
https://www.ncbi.nlm.nih.gov/pubmed/34804849
http://dx.doi.org/10.21037/tau-20-1246
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author Nappi, Lucia
Nichols, Craig
Kollmannsberger, Christian
author_facet Nappi, Lucia
Nichols, Craig
Kollmannsberger, Christian
author_sort Nappi, Lucia
collection PubMed
description Management of testicular germ cell tumor (GCT) patients is based on clinical determinants, mainly CT scan and serum tumor markers (alpha-fetoprotein, beta subunit of HCG and LDH). Treatment decisions are usually straightforward for patients with clear evidence of metastatic disease, confirmed either by imaging tests or by unequivocal elevated tumor markers. However, there are several clinical scenarios where the assessment of metastatic disease is complicated by the limited specificity of the current imaging tests and serum tumor markers. These include patients with clinical stage IIA GCT with negative tumor markers and patients with post-chemotherapy residual disease where, in absence of clear indicators of GCT, decision making and patient treatment allocation become challenging. Therefore, more accurate biomarkers are critical to reduce the risk of under-or over-treatment and to always deliver the most optimal therapy. The objectives of this narrative review are to review the available publications about micro-RNAs in GCT s and their potential clinical applications. Two clusters of micro-RNAs, miR-371a-3p and miR-302/367, specifically expressed by both seminoma and non-seminoma GCT and easily detectable in the peripheral blood, have demonstrated to be promising in this endeavor. Large prospective trials are ongoing to define the operating characteristics of these biomarkers and their clinical utility to improve GCT patient management and reduce the error rate deriving from clinical uncertainty, therefore reducing the risk of sub-optimal treatments.
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spelling pubmed-85755922021-11-18 Narrative review of developing new biomarkers for decision making in advanced testis cancer Nappi, Lucia Nichols, Craig Kollmannsberger, Christian Transl Androl Urol Review Article on Management of Advanced Genitourinary Malignancies Management of testicular germ cell tumor (GCT) patients is based on clinical determinants, mainly CT scan and serum tumor markers (alpha-fetoprotein, beta subunit of HCG and LDH). Treatment decisions are usually straightforward for patients with clear evidence of metastatic disease, confirmed either by imaging tests or by unequivocal elevated tumor markers. However, there are several clinical scenarios where the assessment of metastatic disease is complicated by the limited specificity of the current imaging tests and serum tumor markers. These include patients with clinical stage IIA GCT with negative tumor markers and patients with post-chemotherapy residual disease where, in absence of clear indicators of GCT, decision making and patient treatment allocation become challenging. Therefore, more accurate biomarkers are critical to reduce the risk of under-or over-treatment and to always deliver the most optimal therapy. The objectives of this narrative review are to review the available publications about micro-RNAs in GCT s and their potential clinical applications. Two clusters of micro-RNAs, miR-371a-3p and miR-302/367, specifically expressed by both seminoma and non-seminoma GCT and easily detectable in the peripheral blood, have demonstrated to be promising in this endeavor. Large prospective trials are ongoing to define the operating characteristics of these biomarkers and their clinical utility to improve GCT patient management and reduce the error rate deriving from clinical uncertainty, therefore reducing the risk of sub-optimal treatments. AME Publishing Company 2021-10 /pmc/articles/PMC8575592/ /pubmed/34804849 http://dx.doi.org/10.21037/tau-20-1246 Text en 2021 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review Article on Management of Advanced Genitourinary Malignancies
Nappi, Lucia
Nichols, Craig
Kollmannsberger, Christian
Narrative review of developing new biomarkers for decision making in advanced testis cancer
title Narrative review of developing new biomarkers for decision making in advanced testis cancer
title_full Narrative review of developing new biomarkers for decision making in advanced testis cancer
title_fullStr Narrative review of developing new biomarkers for decision making in advanced testis cancer
title_full_unstemmed Narrative review of developing new biomarkers for decision making in advanced testis cancer
title_short Narrative review of developing new biomarkers for decision making in advanced testis cancer
title_sort narrative review of developing new biomarkers for decision making in advanced testis cancer
topic Review Article on Management of Advanced Genitourinary Malignancies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575592/
https://www.ncbi.nlm.nih.gov/pubmed/34804849
http://dx.doi.org/10.21037/tau-20-1246
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