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Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database

OBJECTIVES: This study performed a competing‐risks analysis using data from the SEER database on penile cancer patients with the aim of identifying more accurate prognostic factors. METHODS: Data on patients with penile cancer were extracted from the SEER database. A univariate analysis used the cum...

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Autores principales: Yang, Jin, Pan, Zhenyu, He, Yujing, Zhao, Fanfan, Feng, Xiaojie, Liu, Qingqing, Lyu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912058/
https://www.ncbi.nlm.nih.gov/pubmed/31657120
http://dx.doi.org/10.1002/cam4.2649
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author Yang, Jin
Pan, Zhenyu
He, Yujing
Zhao, Fanfan
Feng, Xiaojie
Liu, Qingqing
Lyu, Jun
author_facet Yang, Jin
Pan, Zhenyu
He, Yujing
Zhao, Fanfan
Feng, Xiaojie
Liu, Qingqing
Lyu, Jun
author_sort Yang, Jin
collection PubMed
description OBJECTIVES: This study performed a competing‐risks analysis using data from the SEER database on penile cancer patients with the aim of identifying more accurate prognostic factors. METHODS: Data on patients with penile cancer were extracted from the SEER database. A univariate analysis used the cumulative incidence function and Gray's test, while multivariate analysis was performed using the Fine‐Gray model. Cumulative hazards were compared with a competing‐risks model constructed using Kaplan‐Meier estimation. RESULTS: The multivariate Fine‐Gray analysis indicated that being black (HR = 1.51, 95%CI: 1.10‐2.07, P = .01), AJCC stage II (HR = 1.94, 95%CI: 1.36‐2.77, P < .001), AJCC stage III (HR = 1.98, 95%CI: 1.34‐2.91, P < .001), tumor size > 5 cm (HR = 2.23, 95%CI: 1.33‐3.72, P < .05), and TNM stages N1 (HR = 2.49, 95%CI: 1.71‐3.61, P < .001), N2 (HR = 3.25, 95%CI: 2.18‐4.84, P < .001), N3 (HR = 5.05, 95%CI: 2.69‐9.50, P < .001), and M1 (HR = 2.21, 95%CI: 1.28‐3.84, P < .05) were statistically significant. The results obtained using multivariate Cox regression were different, while Kaplan‐Meier curve analysis led to an overestimation of the cumulative risk of the patient. CONCLUSIONS: This study established a competing‐risks analysis model for the first time based on the SEER database for the risk assessment of penile cancer patients. The results may help clinicians to better understand penile cancer and provide these patients with more appropriate support.
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spelling pubmed-69120582019-12-23 Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database Yang, Jin Pan, Zhenyu He, Yujing Zhao, Fanfan Feng, Xiaojie Liu, Qingqing Lyu, Jun Cancer Med Cancer Prevention OBJECTIVES: This study performed a competing‐risks analysis using data from the SEER database on penile cancer patients with the aim of identifying more accurate prognostic factors. METHODS: Data on patients with penile cancer were extracted from the SEER database. A univariate analysis used the cumulative incidence function and Gray's test, while multivariate analysis was performed using the Fine‐Gray model. Cumulative hazards were compared with a competing‐risks model constructed using Kaplan‐Meier estimation. RESULTS: The multivariate Fine‐Gray analysis indicated that being black (HR = 1.51, 95%CI: 1.10‐2.07, P = .01), AJCC stage II (HR = 1.94, 95%CI: 1.36‐2.77, P < .001), AJCC stage III (HR = 1.98, 95%CI: 1.34‐2.91, P < .001), tumor size > 5 cm (HR = 2.23, 95%CI: 1.33‐3.72, P < .05), and TNM stages N1 (HR = 2.49, 95%CI: 1.71‐3.61, P < .001), N2 (HR = 3.25, 95%CI: 2.18‐4.84, P < .001), N3 (HR = 5.05, 95%CI: 2.69‐9.50, P < .001), and M1 (HR = 2.21, 95%CI: 1.28‐3.84, P < .05) were statistically significant. The results obtained using multivariate Cox regression were different, while Kaplan‐Meier curve analysis led to an overestimation of the cumulative risk of the patient. CONCLUSIONS: This study established a competing‐risks analysis model for the first time based on the SEER database for the risk assessment of penile cancer patients. The results may help clinicians to better understand penile cancer and provide these patients with more appropriate support. John Wiley and Sons Inc. 2019-10-27 /pmc/articles/PMC6912058/ /pubmed/31657120 http://dx.doi.org/10.1002/cam4.2649 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Prevention
Yang, Jin
Pan, Zhenyu
He, Yujing
Zhao, Fanfan
Feng, Xiaojie
Liu, Qingqing
Lyu, Jun
Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title_full Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title_fullStr Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title_full_unstemmed Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title_short Competing‐risks model for predicting the prognosis of penile cancer based on the SEER database
title_sort competing‐risks model for predicting the prognosis of penile cancer based on the seer database
topic Cancer Prevention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912058/
https://www.ncbi.nlm.nih.gov/pubmed/31657120
http://dx.doi.org/10.1002/cam4.2649
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