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Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study

Purpose: Lung metastasis is an independent risk factor affecting the prognosis of ovarian cancer patients. We developed and validated a nomogram to predict the risk of synchronous lung metastases in newly diagnosed ovarian cancer patients. Methods: Data of ovarian cancer patients from the Surveillan...

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Autores principales: Yuan, Yufei, Guo, Fanfan, Wang, Ruoran, Zhang, Yidan, Bai, Guiqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687041/
https://www.ncbi.nlm.nih.gov/pubmed/33175143
http://dx.doi.org/10.1042/BSR20203089
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author Yuan, Yufei
Guo, Fanfan
Wang, Ruoran
Zhang, Yidan
Bai, Guiqin
author_facet Yuan, Yufei
Guo, Fanfan
Wang, Ruoran
Zhang, Yidan
Bai, Guiqin
author_sort Yuan, Yufei
collection PubMed
description Purpose: Lung metastasis is an independent risk factor affecting the prognosis of ovarian cancer patients. We developed and validated a nomogram to predict the risk of synchronous lung metastases in newly diagnosed ovarian cancer patients. Methods: Data of ovarian cancer patients from the Surveillance, Epidemiology, and Final Results (SEER) database between 2010 and 2015 were retrospectively collected. The model nomogram was built on the basis of logistic regression. The consistency index (C-index) was used to evaluate the discernment of the synchronous lung metastasis nomogram. Calibration plots were drawn to analyze the consistency between the observed probability and predicted probability of synchronous lung metastases. The Kaplan–Meier method was used to estimate overall survival rate, and influencing factors were included in multivariate Cox regression analysis (P<0.05) to determine the independent prognostic factors of synchronous lung metastases. Results: Overall, 16059 eligible patients were randomly divided into training (n=11242) and validation cohorts (n=4817). AJCC T, N stage, bone metastases, brain metastases, and liver metastases were evaluated as predictors of synchronous lung metastases. Finally, a nomogram was constructed. The nomogram based on independent predictors was calibrated and showed good discriminative ability. Mixed histological types, chemotherapy, and primary site surgery were factors affecting the overall survival of patients with synchronous lung metastases. Conclusion: The clinical prediction model has high accuracy and can be used to predict lung metastasis risk in newly diagnosed ovarian cancer patients, which can guide the treatment of patients with synchronous lung metastases.
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spelling pubmed-76870412020-12-04 Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study Yuan, Yufei Guo, Fanfan Wang, Ruoran Zhang, Yidan Bai, Guiqin Biosci Rep Cancer Purpose: Lung metastasis is an independent risk factor affecting the prognosis of ovarian cancer patients. We developed and validated a nomogram to predict the risk of synchronous lung metastases in newly diagnosed ovarian cancer patients. Methods: Data of ovarian cancer patients from the Surveillance, Epidemiology, and Final Results (SEER) database between 2010 and 2015 were retrospectively collected. The model nomogram was built on the basis of logistic regression. The consistency index (C-index) was used to evaluate the discernment of the synchronous lung metastasis nomogram. Calibration plots were drawn to analyze the consistency between the observed probability and predicted probability of synchronous lung metastases. The Kaplan–Meier method was used to estimate overall survival rate, and influencing factors were included in multivariate Cox regression analysis (P<0.05) to determine the independent prognostic factors of synchronous lung metastases. Results: Overall, 16059 eligible patients were randomly divided into training (n=11242) and validation cohorts (n=4817). AJCC T, N stage, bone metastases, brain metastases, and liver metastases were evaluated as predictors of synchronous lung metastases. Finally, a nomogram was constructed. The nomogram based on independent predictors was calibrated and showed good discriminative ability. Mixed histological types, chemotherapy, and primary site surgery were factors affecting the overall survival of patients with synchronous lung metastases. Conclusion: The clinical prediction model has high accuracy and can be used to predict lung metastasis risk in newly diagnosed ovarian cancer patients, which can guide the treatment of patients with synchronous lung metastases. Portland Press Ltd. 2020-11-24 /pmc/articles/PMC7687041/ /pubmed/33175143 http://dx.doi.org/10.1042/BSR20203089 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the .
spellingShingle Cancer
Yuan, Yufei
Guo, Fanfan
Wang, Ruoran
Zhang, Yidan
Bai, Guiqin
Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title_full Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title_fullStr Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title_full_unstemmed Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title_short Development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
title_sort development and validation of a nomogram to predict synchronous lung metastases in patients with ovarian cancer: a large cohort study
topic Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687041/
https://www.ncbi.nlm.nih.gov/pubmed/33175143
http://dx.doi.org/10.1042/BSR20203089
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