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Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer

Purpose: Nomogram is a widely used tool that precisely predicts individualized cancer prognoses. We aimed to develop and validate a reliable nomogram including serum tumor biomarkers to predict individual overall survival (OS) for patients with resected rectal cancer (RC) and compare the predictive...

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Autores principales: Fan, Shaonan, Li, Ting, Zhou, Ping, Peng, Qiliang, Zhu, Yaqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851506/
https://www.ncbi.nlm.nih.gov/pubmed/31693739
http://dx.doi.org/10.1042/BSR20192636
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author Fan, Shaonan
Li, Ting
Zhou, Ping
Peng, Qiliang
Zhu, Yaqun
author_facet Fan, Shaonan
Li, Ting
Zhou, Ping
Peng, Qiliang
Zhu, Yaqun
author_sort Fan, Shaonan
collection PubMed
description Purpose: Nomogram is a widely used tool that precisely predicts individualized cancer prognoses. We aimed to develop and validate a reliable nomogram including serum tumor biomarkers to predict individual overall survival (OS) for patients with resected rectal cancer (RC) and compare the predictive value with the American Joint Committee on Cancer (AJCC) stages. Patients and methods: We analyzed 520 patients who were diagnosed with non-metastatic rectal cancer as training cohort. External validation was performed in a cohort of 11851 patients from the Surveillance, Epidemiology, and End Results (SEER) database. Independent prognostic factors were identified and integrated to build a nomogram using the Cox proportional hazard regression model. The nomogram was evaluated by Harrell’s concordance index (C-index) and calibration plots in both training and validation cohort. Results: The calibration curves for probability of 1-, 3-, and 5-year OS in both cohorts showed favorable accordance between the nomogram prediction and the actual observation. The C-indices of the nomograms to predict OS were 0.71 in training cohort and 0.69 in the SEER cohort, which were higher than that of the seventh edition American Joint Committee on Cancer TNM staging system for predicting OS (training cohort, 0.71 vs. 0.58, respectively; P-value < 0.001; validation cohort, 0.69 vs. 0.57, respectively; P-value < 0.001). Conclusion: We developed and validated a novel nomogram based on CEA and other factors for predicting OS in patients with resected RC, which could assist clinical decision making and improvement of prognosis prediction for individual RC patients after surgery.
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spelling pubmed-68515062019-11-19 Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer Fan, Shaonan Li, Ting Zhou, Ping Peng, Qiliang Zhu, Yaqun Biosci Rep Diagnostics & Biomarkers Purpose: Nomogram is a widely used tool that precisely predicts individualized cancer prognoses. We aimed to develop and validate a reliable nomogram including serum tumor biomarkers to predict individual overall survival (OS) for patients with resected rectal cancer (RC) and compare the predictive value with the American Joint Committee on Cancer (AJCC) stages. Patients and methods: We analyzed 520 patients who were diagnosed with non-metastatic rectal cancer as training cohort. External validation was performed in a cohort of 11851 patients from the Surveillance, Epidemiology, and End Results (SEER) database. Independent prognostic factors were identified and integrated to build a nomogram using the Cox proportional hazard regression model. The nomogram was evaluated by Harrell’s concordance index (C-index) and calibration plots in both training and validation cohort. Results: The calibration curves for probability of 1-, 3-, and 5-year OS in both cohorts showed favorable accordance between the nomogram prediction and the actual observation. The C-indices of the nomograms to predict OS were 0.71 in training cohort and 0.69 in the SEER cohort, which were higher than that of the seventh edition American Joint Committee on Cancer TNM staging system for predicting OS (training cohort, 0.71 vs. 0.58, respectively; P-value < 0.001; validation cohort, 0.69 vs. 0.57, respectively; P-value < 0.001). Conclusion: We developed and validated a novel nomogram based on CEA and other factors for predicting OS in patients with resected RC, which could assist clinical decision making and improvement of prognosis prediction for individual RC patients after surgery. Portland Press Ltd. 2019-11-13 /pmc/articles/PMC6851506/ /pubmed/31693739 http://dx.doi.org/10.1042/BSR20192636 Text en © 2019 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 Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Diagnostics & Biomarkers
Fan, Shaonan
Li, Ting
Zhou, Ping
Peng, Qiliang
Zhu, Yaqun
Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title_full Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title_fullStr Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title_full_unstemmed Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title_short Development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
title_sort development and validation of nomogram combining serum biomarker for predicting survival in patients with resected rectal cancer
topic Diagnostics & Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851506/
https://www.ncbi.nlm.nih.gov/pubmed/31693739
http://dx.doi.org/10.1042/BSR20192636
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