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Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance

BACKGROUND: We aimed to validate Decipher to predict adverse pathology (AP) at radical prostatectomy (RP) in men with National Comprehensive Cancer Network (NCCN) favorable-intermediate risk (F-IR) prostate cancer (PCa), and to better select F-IR candidates for active surveillance (AS). METHODS: In...

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Autores principales: Herlemann, Annika, Huang, Huei-Chung, Alam, Ridwan, Tosoian, Jeffery J., Kim, Hyung L., Klein, Eric A., Simko, Jeffry P., Chan, June M., Lane, Brian R., Davis, John W., Davicioni, Elai, Feng, Felix Y., McCue, Peter, Kim, Hyun, Den, Robert B., Bismar, Tarek A., Carroll, Peter R., Cooperberg, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076042/
https://www.ncbi.nlm.nih.gov/pubmed/31455846
http://dx.doi.org/10.1038/s41391-019-0167-9
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author Herlemann, Annika
Huang, Huei-Chung
Alam, Ridwan
Tosoian, Jeffery J.
Kim, Hyung L.
Klein, Eric A.
Simko, Jeffry P.
Chan, June M.
Lane, Brian R.
Davis, John W.
Davicioni, Elai
Feng, Felix Y.
McCue, Peter
Kim, Hyun
Den, Robert B.
Bismar, Tarek A.
Carroll, Peter R.
Cooperberg, Matthew R.
author_facet Herlemann, Annika
Huang, Huei-Chung
Alam, Ridwan
Tosoian, Jeffery J.
Kim, Hyung L.
Klein, Eric A.
Simko, Jeffry P.
Chan, June M.
Lane, Brian R.
Davis, John W.
Davicioni, Elai
Feng, Felix Y.
McCue, Peter
Kim, Hyun
Den, Robert B.
Bismar, Tarek A.
Carroll, Peter R.
Cooperberg, Matthew R.
author_sort Herlemann, Annika
collection PubMed
description BACKGROUND: We aimed to validate Decipher to predict adverse pathology (AP) at radical prostatectomy (RP) in men with National Comprehensive Cancer Network (NCCN) favorable-intermediate risk (F-IR) prostate cancer (PCa), and to better select F-IR candidates for active surveillance (AS). METHODS: In all, 647 patients diagnosed with NCCN very low/low risk (VL/LR) or F-IR prostate cancer were identified from a multi-institutional PCa biopsy database; all underwent RP with complete postoperative clinicopathological information and Decipher genomic risk scores. The performance of all risk assessment tools was evaluated using logistic regression model for the endpoint of AP, defined as grade group 3−5, pT3b or higher, or lymph node invasion. RESULTS: The median age was 61 years (interquartile range 56–66) for 220 patients with NCCN F-IR disease, 53% classified as low-risk by Cancer of the Prostate Risk Assessment (CAPRA 0−2) and 47% as intermediate-risk (CAPRA 3−5). Decipher classified 79%, 13% and 8% of men as low-, intermediate- and high-risk with 13%, 10%, and 41% rate of AP, respectively. Decipher was an independent predictor of AP with an odds ratio of 1.34 per 0.1 unit increased (p value = 0.002) and remained significant when adjusting by CAPRA. Notably, F-IR with Decipher low or intermediate score did not associate with significantly higher odds of AP compared to VL/LR. CONCLUSIONS: NCCN risk groups, including F-IR, are highly heterogeneous and should be replaced with multivariable risk-stratification. In particular, incorporating Decipher may be useful for safely expanding the use of AS in this patient population.
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spelling pubmed-80760422021-05-06 Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance Herlemann, Annika Huang, Huei-Chung Alam, Ridwan Tosoian, Jeffery J. Kim, Hyung L. Klein, Eric A. Simko, Jeffry P. Chan, June M. Lane, Brian R. Davis, John W. Davicioni, Elai Feng, Felix Y. McCue, Peter Kim, Hyun Den, Robert B. Bismar, Tarek A. Carroll, Peter R. Cooperberg, Matthew R. Prostate Cancer Prostatic Dis Article BACKGROUND: We aimed to validate Decipher to predict adverse pathology (AP) at radical prostatectomy (RP) in men with National Comprehensive Cancer Network (NCCN) favorable-intermediate risk (F-IR) prostate cancer (PCa), and to better select F-IR candidates for active surveillance (AS). METHODS: In all, 647 patients diagnosed with NCCN very low/low risk (VL/LR) or F-IR prostate cancer were identified from a multi-institutional PCa biopsy database; all underwent RP with complete postoperative clinicopathological information and Decipher genomic risk scores. The performance of all risk assessment tools was evaluated using logistic regression model for the endpoint of AP, defined as grade group 3−5, pT3b or higher, or lymph node invasion. RESULTS: The median age was 61 years (interquartile range 56–66) for 220 patients with NCCN F-IR disease, 53% classified as low-risk by Cancer of the Prostate Risk Assessment (CAPRA 0−2) and 47% as intermediate-risk (CAPRA 3−5). Decipher classified 79%, 13% and 8% of men as low-, intermediate- and high-risk with 13%, 10%, and 41% rate of AP, respectively. Decipher was an independent predictor of AP with an odds ratio of 1.34 per 0.1 unit increased (p value = 0.002) and remained significant when adjusting by CAPRA. Notably, F-IR with Decipher low or intermediate score did not associate with significantly higher odds of AP compared to VL/LR. CONCLUSIONS: NCCN risk groups, including F-IR, are highly heterogeneous and should be replaced with multivariable risk-stratification. In particular, incorporating Decipher may be useful for safely expanding the use of AS in this patient population. Nature Publishing Group UK 2019-08-27 2020 /pmc/articles/PMC8076042/ /pubmed/31455846 http://dx.doi.org/10.1038/s41391-019-0167-9 Text en © The Author(s) 2019 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 Article
Herlemann, Annika
Huang, Huei-Chung
Alam, Ridwan
Tosoian, Jeffery J.
Kim, Hyung L.
Klein, Eric A.
Simko, Jeffry P.
Chan, June M.
Lane, Brian R.
Davis, John W.
Davicioni, Elai
Feng, Felix Y.
McCue, Peter
Kim, Hyun
Den, Robert B.
Bismar, Tarek A.
Carroll, Peter R.
Cooperberg, Matthew R.
Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title_full Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title_fullStr Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title_full_unstemmed Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title_short Decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
title_sort decipher identifies men with otherwise clinically favorable-intermediate risk disease who may not be good candidates for active surveillance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076042/
https://www.ncbi.nlm.nih.gov/pubmed/31455846
http://dx.doi.org/10.1038/s41391-019-0167-9
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