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Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study

BACKGROUND: The purpose of this present research was to construct a nomograph model to predict prognosis in gallbladder cancer liver metastasis (GCLM) patients so as to provide a basis for clinical decision-making. METHODS: We surveyed patients diagnosed with GCLM in the Surveillance Epidemiology an...

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Autores principales: Zhang, Woods, Chen, Zhitian, Sa, Benzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695336/
https://www.ncbi.nlm.nih.gov/pubmed/37994618
http://dx.doi.org/10.1097/MEG.0000000000002678
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author Zhang, Woods
Chen, Zhitian
Sa, Benzhong
author_facet Zhang, Woods
Chen, Zhitian
Sa, Benzhong
author_sort Zhang, Woods
collection PubMed
description BACKGROUND: The purpose of this present research was to construct a nomograph model to predict prognosis in gallbladder cancer liver metastasis (GCLM) patients so as to provide a basis for clinical decision-making. METHODS: We surveyed patients diagnosed with GCLM in the Surveillance Epidemiology and the End Results database between 2010 and 2019. They were randomized 7 : 3 into a training set and a validation set. In the training set, meaningful prognostic factors were determined using univariate and multivariate Cox regression analyses, and an individualized nomogram prediction model was generated. The prediction model was evaluated by C-index, calibration curve, ROC curve and DCA curve from the training set and the validation set. RESULTS: A total of 727 confirmed cases were enrolled in the research, 510 in the training set and 217 in the validation set. Factors including bone metastasis, surgery, chemotherapy and radiotherapy were independent prognostic factors for cancer-specific survival (CSS) rates and were employed in the construction of the nomogram model. The C-index for the training set and validation set were 0.688 and 0.708, respectively. The calibration curve exhibited good consistency between predicted and actual CSS rates. ROC curve and DCA of the nomogram showed superior performance at 6 months CSS, 1-year CSS and 2 years CSS in both the training set and validation set. CONCLUSION: We have successfully constructed a nomogram model that can predict CSS rates in patients with GCLM. This prediction model can help patients in counseling and guide clinicians in treatment decisions.
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spelling pubmed-106953362023-12-05 Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study Zhang, Woods Chen, Zhitian Sa, Benzhong Eur J Gastroenterol Hepatol Original Articles: Hepatology BACKGROUND: The purpose of this present research was to construct a nomograph model to predict prognosis in gallbladder cancer liver metastasis (GCLM) patients so as to provide a basis for clinical decision-making. METHODS: We surveyed patients diagnosed with GCLM in the Surveillance Epidemiology and the End Results database between 2010 and 2019. They were randomized 7 : 3 into a training set and a validation set. In the training set, meaningful prognostic factors were determined using univariate and multivariate Cox regression analyses, and an individualized nomogram prediction model was generated. The prediction model was evaluated by C-index, calibration curve, ROC curve and DCA curve from the training set and the validation set. RESULTS: A total of 727 confirmed cases were enrolled in the research, 510 in the training set and 217 in the validation set. Factors including bone metastasis, surgery, chemotherapy and radiotherapy were independent prognostic factors for cancer-specific survival (CSS) rates and were employed in the construction of the nomogram model. The C-index for the training set and validation set were 0.688 and 0.708, respectively. The calibration curve exhibited good consistency between predicted and actual CSS rates. ROC curve and DCA of the nomogram showed superior performance at 6 months CSS, 1-year CSS and 2 years CSS in both the training set and validation set. CONCLUSION: We have successfully constructed a nomogram model that can predict CSS rates in patients with GCLM. This prediction model can help patients in counseling and guide clinicians in treatment decisions. Lippincott Williams And Wilkins 2023-11-23 2024-01 /pmc/articles/PMC10695336/ /pubmed/37994618 http://dx.doi.org/10.1097/MEG.0000000000002678 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Articles: Hepatology
Zhang, Woods
Chen, Zhitian
Sa, Benzhong
Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title_full Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title_fullStr Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title_full_unstemmed Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title_short Construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a SEER-based study
title_sort construction and validation of the predictive model for gallbladder cancer liver metastasis patients: a seer-based study
topic Original Articles: Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10695336/
https://www.ncbi.nlm.nih.gov/pubmed/37994618
http://dx.doi.org/10.1097/MEG.0000000000002678
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