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Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study
BACKGROUND: The aim was to evaluate the prognosis of men with all possible high-risk prostate cancers (PCa) stratified by risk factors. METHODS: Within the Surveillance, Epidemiology and End Results (SEER) database from 2004 to 2015, men with non-metastasis high-risk PCa were identified. Kaplan-Meie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797365/ https://www.ncbi.nlm.nih.gov/pubmed/35117213 http://dx.doi.org/10.21037/tcr-20-1578 |
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author | Song, Pan Wang, Jiaxiang Shu, Mengxuan Di, Xiaoyu Li, Yaxin Qing, Yuxin Dong, Qiang |
author_facet | Song, Pan Wang, Jiaxiang Shu, Mengxuan Di, Xiaoyu Li, Yaxin Qing, Yuxin Dong, Qiang |
author_sort | Song, Pan |
collection | PubMed |
description | BACKGROUND: The aim was to evaluate the prognosis of men with all possible high-risk prostate cancers (PCa) stratified by risk factors. METHODS: Within the Surveillance, Epidemiology and End Results (SEER) database from 2004 to 2015, men with non-metastasis high-risk PCa were identified. Kaplan-Meier analysis and Cox regressions were adopted to evaluate the overall survival (OS) and prostate cancer-specific survival (PCSS). Nomograms were conducted to build a predictive model. Concordance index (C-index) and calibration curves were used to validate the model. RESULTS: A total of 151,799 patients were included. Seven risk groups were divided including one high-risk factor of T3–4 (A1), prostate-specific antigen (PSA) >20 ng/mL (A2), and Gleason score (GS) 8–10, two high-risk factors of T3–4 PSA >20 ng/mL (B1), T3–4 GS 8–10 (B2), PSA >20 ng/mL GS 8–10 (B3), and three high-risk factors of T3–4 PSA >20 ng/mL GS 8–10 (C). The survival curves of PCSS showed that A1 was the best among all groups. A2, A3 and B1 had similar results and were all better than B2 [with A2 as reference, A3 hazard ratio (HR): 1.09 (1.02–1.17), P=0.046; B1 HR: 0.93 (0.82–1.05), P=0.103; B2 HR: 1.42 (1.32–1.53), P<0.001]. There is no significant difference between B3 and C [HR: 0.94 (0.86–1.03), P=0.029] and these two present the worst survival in prognosis. The 10-year PCSS of A1, A2, A3, B1, B2, B3, and C groups were 95.8%, 86.9%, 86.1%, 86.9%, 80.8%, 64.7% and 65.6%, respectively. Three simplified groups were divided including a good prognosis group (A1), an intermediate prognosis group (A2, A3, B1 and B2), and a poor prognosis group (B3 and C). Compared to the good prognosis group, the HR of the intermediate and the poor prognosis group were 4.21 (3.96–4.48), P<0.001 and 11.36 (10.59–12.19), P<0.001. A nomogram was built based on these factors. The C-index of the nomogram was 0.772, indicating a good accuracy of the model. CONCLUSIONS: Men with the combination of PSA >20 ng/mL and GS 8–10 had the worst PCSS among all patients. PCa with three high-risk factors was not more aggressive than that with two high-risk factors of GS 8–10 and PSA >20 ng/mL. |
format | Online Article Text |
id | pubmed-8797365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87973652022-02-02 Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study Song, Pan Wang, Jiaxiang Shu, Mengxuan Di, Xiaoyu Li, Yaxin Qing, Yuxin Dong, Qiang Transl Cancer Res Original Article BACKGROUND: The aim was to evaluate the prognosis of men with all possible high-risk prostate cancers (PCa) stratified by risk factors. METHODS: Within the Surveillance, Epidemiology and End Results (SEER) database from 2004 to 2015, men with non-metastasis high-risk PCa were identified. Kaplan-Meier analysis and Cox regressions were adopted to evaluate the overall survival (OS) and prostate cancer-specific survival (PCSS). Nomograms were conducted to build a predictive model. Concordance index (C-index) and calibration curves were used to validate the model. RESULTS: A total of 151,799 patients were included. Seven risk groups were divided including one high-risk factor of T3–4 (A1), prostate-specific antigen (PSA) >20 ng/mL (A2), and Gleason score (GS) 8–10, two high-risk factors of T3–4 PSA >20 ng/mL (B1), T3–4 GS 8–10 (B2), PSA >20 ng/mL GS 8–10 (B3), and three high-risk factors of T3–4 PSA >20 ng/mL GS 8–10 (C). The survival curves of PCSS showed that A1 was the best among all groups. A2, A3 and B1 had similar results and were all better than B2 [with A2 as reference, A3 hazard ratio (HR): 1.09 (1.02–1.17), P=0.046; B1 HR: 0.93 (0.82–1.05), P=0.103; B2 HR: 1.42 (1.32–1.53), P<0.001]. There is no significant difference between B3 and C [HR: 0.94 (0.86–1.03), P=0.029] and these two present the worst survival in prognosis. The 10-year PCSS of A1, A2, A3, B1, B2, B3, and C groups were 95.8%, 86.9%, 86.1%, 86.9%, 80.8%, 64.7% and 65.6%, respectively. Three simplified groups were divided including a good prognosis group (A1), an intermediate prognosis group (A2, A3, B1 and B2), and a poor prognosis group (B3 and C). Compared to the good prognosis group, the HR of the intermediate and the poor prognosis group were 4.21 (3.96–4.48), P<0.001 and 11.36 (10.59–12.19), P<0.001. A nomogram was built based on these factors. The C-index of the nomogram was 0.772, indicating a good accuracy of the model. CONCLUSIONS: Men with the combination of PSA >20 ng/mL and GS 8–10 had the worst PCSS among all patients. PCa with three high-risk factors was not more aggressive than that with two high-risk factors of GS 8–10 and PSA >20 ng/mL. AME Publishing Company 2020-10 /pmc/articles/PMC8797365/ /pubmed/35117213 http://dx.doi.org/10.21037/tcr-20-1578 Text en 2020 Translational Cancer Research. 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/. |
spellingShingle | Original Article Song, Pan Wang, Jiaxiang Shu, Mengxuan Di, Xiaoyu Li, Yaxin Qing, Yuxin Dong, Qiang Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title | Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title_full | Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title_fullStr | Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title_full_unstemmed | Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title_short | Prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
title_sort | prognosis of men with high-risk prostate cancer stratified by risk factors: a population-based retrospective cohort study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797365/ https://www.ncbi.nlm.nih.gov/pubmed/35117213 http://dx.doi.org/10.21037/tcr-20-1578 |
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