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Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score

AIM: To evaluate active surveillance (AS) selection, safety and durability among men with low-risk prostate cancer assessed using the clinical cell cycle risk (CCR) score, a combined clinical and molecular score. PATIENTS & METHODS: Initial treatment selection (AS vs treatment) and duration of A...

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Autores principales: Kaul, Sanjeev, Wojno, Kirk J, Stone, Steven, Evans, Brent, Bernhisel, Ryan, Meek, Stephanie, D’Anna, Richard E, Ferguson, Jeffrey, Glaser, Jeffrey, Morgan, Todd M, Lieb, Jeremy, Yan, Robert, Cohen, Todd, Ehdaie, Behfar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447833/
https://www.ncbi.nlm.nih.gov/pubmed/31483217
http://dx.doi.org/10.2217/pme-2019-0084
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author Kaul, Sanjeev
Wojno, Kirk J
Stone, Steven
Evans, Brent
Bernhisel, Ryan
Meek, Stephanie
D’Anna, Richard E
Ferguson, Jeffrey
Glaser, Jeffrey
Morgan, Todd M
Lieb, Jeremy
Yan, Robert
Cohen, Todd
Ehdaie, Behfar
author_facet Kaul, Sanjeev
Wojno, Kirk J
Stone, Steven
Evans, Brent
Bernhisel, Ryan
Meek, Stephanie
D’Anna, Richard E
Ferguson, Jeffrey
Glaser, Jeffrey
Morgan, Todd M
Lieb, Jeremy
Yan, Robert
Cohen, Todd
Ehdaie, Behfar
author_sort Kaul, Sanjeev
collection PubMed
description AIM: To evaluate active surveillance (AS) selection, safety and durability among men with low-risk prostate cancer assessed using the clinical cell cycle risk (CCR) score, a combined clinical and molecular score. PATIENTS & METHODS: Initial treatment selection (AS vs treatment) and duration of AS were evaluated for men with low-risk prostate cancer according to the CCR score and National Comprehensive Cancer Network guidelines. Adverse events included biochemical recurrence and metastasis. RESULTS: 82.4% (547/664) of men initially selected AS (median follow-up: 2.2 years), 0.4% (2/547) of whom experienced an adverse event. Two-thirds of patients remained on AS for more than 3 years; patient choice was the most common reason for leaving AS. CONCLUSION: The CCR score may aid in the identification of men who can safely defer prostate cancer treatment.
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spelling pubmed-74478332020-08-31 Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score Kaul, Sanjeev Wojno, Kirk J Stone, Steven Evans, Brent Bernhisel, Ryan Meek, Stephanie D’Anna, Richard E Ferguson, Jeffrey Glaser, Jeffrey Morgan, Todd M Lieb, Jeremy Yan, Robert Cohen, Todd Ehdaie, Behfar Per Med Research Article AIM: To evaluate active surveillance (AS) selection, safety and durability among men with low-risk prostate cancer assessed using the clinical cell cycle risk (CCR) score, a combined clinical and molecular score. PATIENTS & METHODS: Initial treatment selection (AS vs treatment) and duration of AS were evaluated for men with low-risk prostate cancer according to the CCR score and National Comprehensive Cancer Network guidelines. Adverse events included biochemical recurrence and metastasis. RESULTS: 82.4% (547/664) of men initially selected AS (median follow-up: 2.2 years), 0.4% (2/547) of whom experienced an adverse event. Two-thirds of patients remained on AS for more than 3 years; patient choice was the most common reason for leaving AS. CONCLUSION: The CCR score may aid in the identification of men who can safely defer prostate cancer treatment. Future Medicine Ltd 2019-09-04 2019-11 /pmc/articles/PMC7447833/ /pubmed/31483217 http://dx.doi.org/10.2217/pme-2019-0084 Text en © 2019 Sanjeev Kaul et al. This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Research Article
Kaul, Sanjeev
Wojno, Kirk J
Stone, Steven
Evans, Brent
Bernhisel, Ryan
Meek, Stephanie
D’Anna, Richard E
Ferguson, Jeffrey
Glaser, Jeffrey
Morgan, Todd M
Lieb, Jeremy
Yan, Robert
Cohen, Todd
Ehdaie, Behfar
Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title_full Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title_fullStr Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title_full_unstemmed Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title_short Clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
title_sort clinical outcomes in men with prostate cancer who selected active surveillance using a clinical cell cycle risk score
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447833/
https://www.ncbi.nlm.nih.gov/pubmed/31483217
http://dx.doi.org/10.2217/pme-2019-0084
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