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Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study

BACKGROUND: Ovarian cancer remains the most lethal gynecologic malignancy. In this study, we aimed to identify the specific risk factors affecting overall survival (OS) and develop a nomogram for prognostic prediction of ovarian cancer patients based on data from the Surveillance, Epidemiology, and...

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Autores principales: Sun, Huizhen, Yan, Li, Chen, Hainan, Zheng, Tao, Zhang, Yi, Wang, Husheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799304/
https://www.ncbi.nlm.nih.gov/pubmed/35117197
http://dx.doi.org/10.21037/tcr-20-1238
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author Sun, Huizhen
Yan, Li
Chen, Hainan
Zheng, Tao
Zhang, Yi
Wang, Husheng
author_facet Sun, Huizhen
Yan, Li
Chen, Hainan
Zheng, Tao
Zhang, Yi
Wang, Husheng
author_sort Sun, Huizhen
collection PubMed
description BACKGROUND: Ovarian cancer remains the most lethal gynecologic malignancy. In this study, we aimed to identify the specific risk factors affecting overall survival (OS) and develop a nomogram for prognostic prediction of ovarian cancer patients based on data from the Surveillance, Epidemiology, and End Results (SEER) database. METHODS: Information from the SEER database on ovarian cancer between 2004 and 2016 was screened and retrieved. Cases were randomly divided into the training cohort hand the validation cohort at a 7:3 ratio. The prognostic effects of individual variables on survival were evaluated via Kaplan-Meier method and Cox proportional hazards regression model using data from the training cohort. A nomogram was formulated to predict the 3- and 5-year OS rates of patients with ovarian cancer, and then validated both in the training cohort and the validation cohort. RESULTS: A total of 28,375 patients were selected from 75,921 samples (19,862 in training cohort and 8,513 in validation cohort). Cox regression analysis identified race, age laterality, histology, stage, grade, surgery, chemotherapy, radiotherapy, and marital status as independent risk factors for ovarian cancer prognosis. A nomogram was developed based on the results of multivariate analysis and validated using an internal bootstrap resampling approach, which demonstrated a sufficient level of discrimination according to the C-index (0.752, 95% CI: 0.746–0.758 in the training cohort, 0.755, 95% CI: 0.746–0.764). CONCLUSIONS: We developed a nomogram valuable for accurate prediction of 3- and 5-year OS rates of ovarian cancer patients based on individual characteristics.
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spelling pubmed-87993042022-02-02 Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study Sun, Huizhen Yan, Li Chen, Hainan Zheng, Tao Zhang, Yi Wang, Husheng Transl Cancer Res Original Article BACKGROUND: Ovarian cancer remains the most lethal gynecologic malignancy. In this study, we aimed to identify the specific risk factors affecting overall survival (OS) and develop a nomogram for prognostic prediction of ovarian cancer patients based on data from the Surveillance, Epidemiology, and End Results (SEER) database. METHODS: Information from the SEER database on ovarian cancer between 2004 and 2016 was screened and retrieved. Cases were randomly divided into the training cohort hand the validation cohort at a 7:3 ratio. The prognostic effects of individual variables on survival were evaluated via Kaplan-Meier method and Cox proportional hazards regression model using data from the training cohort. A nomogram was formulated to predict the 3- and 5-year OS rates of patients with ovarian cancer, and then validated both in the training cohort and the validation cohort. RESULTS: A total of 28,375 patients were selected from 75,921 samples (19,862 in training cohort and 8,513 in validation cohort). Cox regression analysis identified race, age laterality, histology, stage, grade, surgery, chemotherapy, radiotherapy, and marital status as independent risk factors for ovarian cancer prognosis. A nomogram was developed based on the results of multivariate analysis and validated using an internal bootstrap resampling approach, which demonstrated a sufficient level of discrimination according to the C-index (0.752, 95% CI: 0.746–0.758 in the training cohort, 0.755, 95% CI: 0.746–0.764). CONCLUSIONS: We developed a nomogram valuable for accurate prediction of 3- and 5-year OS rates of ovarian cancer patients based on individual characteristics. AME Publishing Company 2020-10 /pmc/articles/PMC8799304/ /pubmed/35117197 http://dx.doi.org/10.21037/tcr-20-1238 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
Sun, Huizhen
Yan, Li
Chen, Hainan
Zheng, Tao
Zhang, Yi
Wang, Husheng
Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title_full Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title_fullStr Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title_full_unstemmed Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title_short Development of a nomogram to predict prognosis in ovarian cancer: a SEER-based study
title_sort development of a nomogram to predict prognosis in ovarian cancer: a seer-based study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8799304/
https://www.ncbi.nlm.nih.gov/pubmed/35117197
http://dx.doi.org/10.21037/tcr-20-1238
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