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Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients

OBJECTIVE: To explore the factors affecting the prognosis of cervical cancer (CC), and to construct and evaluate predictive nomograms to guide individualized clinical treatment. METHODS: The clinicopathological and follow‐up data of CC patients from June 2013 to December 2019 in Sun Yat‐sen Memorial...

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Autores principales: Rao, Qunxian, Han, Xue, Wei, Yuan, Zhou, Hui, Gong, Yajie, Guan, Meimei, Feng, Xiaoyan, Lu, Huaiwu, Chen, Qingsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028162/
https://www.ncbi.nlm.nih.gov/pubmed/36394197
http://dx.doi.org/10.1002/cam4.5335
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author Rao, Qunxian
Han, Xue
Wei, Yuan
Zhou, Hui
Gong, Yajie
Guan, Meimei
Feng, Xiaoyan
Lu, Huaiwu
Chen, Qingsong
author_facet Rao, Qunxian
Han, Xue
Wei, Yuan
Zhou, Hui
Gong, Yajie
Guan, Meimei
Feng, Xiaoyan
Lu, Huaiwu
Chen, Qingsong
author_sort Rao, Qunxian
collection PubMed
description OBJECTIVE: To explore the factors affecting the prognosis of cervical cancer (CC), and to construct and evaluate predictive nomograms to guide individualized clinical treatment. METHODS: The clinicopathological and follow‐up data of CC patients from June 2013 to December 2019 in Sun Yat‐sen Memorial Hospital of Sun Yat‐sen University were retrospectively analyzed. Log‐rank test was used for univariate survival analysis, and Cox multivariate regression was used to identify independent prognostic factors, based on which nomogram models were established and evaluated in multiple aspects. RESULTS: Patients were randomly assigned into the training (n = 746) and validation sets (n = 329). Survival analysis of the training set identified cervical myometrial invasion, parametrial involvement, and malignant tumor history as prognosticators of postoperative DFS and pathological type, cervical myometrial invasion, and history of STD for OS. C‐index was 0.799 and 0.839 for the nomograms for DFS and OS, respectively. Calibration curves and Brier scores also indicated high performance. Importantly, decision curve analysis suggested great clinical applicability of these nomograms. CONCLUSIONS: In this study, we analyzed a cohort of 1075 CC patients and identified DFS‐ or OS‐associated clinicohistologic characteristics. Two nomograms were subsequently constructed for DFS and OS prognostication, respectively, and showed high performance in terms of discrimination, calibration, and clinical applicability. These models may facilitate individualized treatment and patient selection for clinical trials. Future investigations with larger cohorts and prospective designs are warranted for validating these prognostic models.
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spelling pubmed-100281622023-03-22 Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients Rao, Qunxian Han, Xue Wei, Yuan Zhou, Hui Gong, Yajie Guan, Meimei Feng, Xiaoyan Lu, Huaiwu Chen, Qingsong Cancer Med RESEARCH ARTICLES OBJECTIVE: To explore the factors affecting the prognosis of cervical cancer (CC), and to construct and evaluate predictive nomograms to guide individualized clinical treatment. METHODS: The clinicopathological and follow‐up data of CC patients from June 2013 to December 2019 in Sun Yat‐sen Memorial Hospital of Sun Yat‐sen University were retrospectively analyzed. Log‐rank test was used for univariate survival analysis, and Cox multivariate regression was used to identify independent prognostic factors, based on which nomogram models were established and evaluated in multiple aspects. RESULTS: Patients were randomly assigned into the training (n = 746) and validation sets (n = 329). Survival analysis of the training set identified cervical myometrial invasion, parametrial involvement, and malignant tumor history as prognosticators of postoperative DFS and pathological type, cervical myometrial invasion, and history of STD for OS. C‐index was 0.799 and 0.839 for the nomograms for DFS and OS, respectively. Calibration curves and Brier scores also indicated high performance. Importantly, decision curve analysis suggested great clinical applicability of these nomograms. CONCLUSIONS: In this study, we analyzed a cohort of 1075 CC patients and identified DFS‐ or OS‐associated clinicohistologic characteristics. Two nomograms were subsequently constructed for DFS and OS prognostication, respectively, and showed high performance in terms of discrimination, calibration, and clinical applicability. These models may facilitate individualized treatment and patient selection for clinical trials. Future investigations with larger cohorts and prospective designs are warranted for validating these prognostic models. John Wiley and Sons Inc. 2022-11-16 /pmc/articles/PMC10028162/ /pubmed/36394197 http://dx.doi.org/10.1002/cam4.5335 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Rao, Qunxian
Han, Xue
Wei, Yuan
Zhou, Hui
Gong, Yajie
Guan, Meimei
Feng, Xiaoyan
Lu, Huaiwu
Chen, Qingsong
Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title_full Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title_fullStr Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title_full_unstemmed Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title_short Novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
title_sort novel prognostic nomograms in cervical cancer based on analysis of 1075 patients
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028162/
https://www.ncbi.nlm.nih.gov/pubmed/36394197
http://dx.doi.org/10.1002/cam4.5335
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