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Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers
BACKGROUND: Early hepatocellular carcinoma (HCC) detection with non-invasive biomarkers remains an unmet clinical need. We aimed to construct a predictive model based on the pre-diagnostic levels of serum markers to predict the early-stage onset of HCC. METHODS: A total of 339 HCC patients (includin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472335/ https://www.ncbi.nlm.nih.gov/pubmed/36100887 http://dx.doi.org/10.1186/s12876-022-02489-2 |
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author | Zheng, Liming Huang, Zeyu Li, Xiaoping He, Meifang Liu, Xiaoqin Zheng, Guojun Zhou, Xike Liu, Longgen |
author_facet | Zheng, Liming Huang, Zeyu Li, Xiaoping He, Meifang Liu, Xiaoqin Zheng, Guojun Zhou, Xike Liu, Longgen |
author_sort | Zheng, Liming |
collection | PubMed |
description | BACKGROUND: Early hepatocellular carcinoma (HCC) detection with non-invasive biomarkers remains an unmet clinical need. We aimed to construct a predictive model based on the pre-diagnostic levels of serum markers to predict the early-stage onset of HCC. METHODS: A total of 339 HCC patients (including 157 patients from Changzhou cohort and 182 patients from Wuxi cohort) were enrolled in our retrospective study. Levels of 25 baseline serum markers were collected. Propensity score matching (PSM) analysis was conducted to balance the distributions of patients’ gender, age, and the surveillance time between HCC group and control group. Then, Receiver operating characteristic (ROC) and Logistic regression analysis were performed to screen the independent predictive variables and construct a non-invasive predictive model. Subsequently, ROC curve and Kaplan–Meier (K–M) curve were used to evaluate the predictive values of the model. Clinical net benefit of the model was demonstrated by decision curve analysis (DCA) and clinical impact curve. RESULTS: Five independent predictive variables for HCC onset and two general characteristics of patients (age and gender) were incorporated into the score model. ROC and DCA curves showed that the score model had better predictive performance in discrimination and clinical net benefit compared with single variable or other score systems, with the area under the curve (AUC) of 0.890 (95% CI 0.856–0.925) in Changzhou cohort and 0.799 (95% CI 0.751–0.849) in Wuxi cohort. Meanwhile, stratification analysis indicated that the score model had good predictive values for patients with early tumor stage (AJCC stage I) or small tumors (< 2 cm). Moreover, the score of HCC patient began to increase at 30 months before clinical diagnosis and reach a peak at 6 months. CONCLUSION: Based on this model, we could optimize the current risk stratification at an early stage and consider further intensive surveillance programs for high-risk patients. It could also help clinicians to evaluate the progression and predict the prognosis of HCC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02489-2. |
format | Online Article Text |
id | pubmed-9472335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94723352022-09-15 Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers Zheng, Liming Huang, Zeyu Li, Xiaoping He, Meifang Liu, Xiaoqin Zheng, Guojun Zhou, Xike Liu, Longgen BMC Gastroenterol Research BACKGROUND: Early hepatocellular carcinoma (HCC) detection with non-invasive biomarkers remains an unmet clinical need. We aimed to construct a predictive model based on the pre-diagnostic levels of serum markers to predict the early-stage onset of HCC. METHODS: A total of 339 HCC patients (including 157 patients from Changzhou cohort and 182 patients from Wuxi cohort) were enrolled in our retrospective study. Levels of 25 baseline serum markers were collected. Propensity score matching (PSM) analysis was conducted to balance the distributions of patients’ gender, age, and the surveillance time between HCC group and control group. Then, Receiver operating characteristic (ROC) and Logistic regression analysis were performed to screen the independent predictive variables and construct a non-invasive predictive model. Subsequently, ROC curve and Kaplan–Meier (K–M) curve were used to evaluate the predictive values of the model. Clinical net benefit of the model was demonstrated by decision curve analysis (DCA) and clinical impact curve. RESULTS: Five independent predictive variables for HCC onset and two general characteristics of patients (age and gender) were incorporated into the score model. ROC and DCA curves showed that the score model had better predictive performance in discrimination and clinical net benefit compared with single variable or other score systems, with the area under the curve (AUC) of 0.890 (95% CI 0.856–0.925) in Changzhou cohort and 0.799 (95% CI 0.751–0.849) in Wuxi cohort. Meanwhile, stratification analysis indicated that the score model had good predictive values for patients with early tumor stage (AJCC stage I) or small tumors (< 2 cm). Moreover, the score of HCC patient began to increase at 30 months before clinical diagnosis and reach a peak at 6 months. CONCLUSION: Based on this model, we could optimize the current risk stratification at an early stage and consider further intensive surveillance programs for high-risk patients. It could also help clinicians to evaluate the progression and predict the prognosis of HCC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02489-2. BioMed Central 2022-09-13 /pmc/articles/PMC9472335/ /pubmed/36100887 http://dx.doi.org/10.1186/s12876-022-02489-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zheng, Liming Huang, Zeyu Li, Xiaoping He, Meifang Liu, Xiaoqin Zheng, Guojun Zhou, Xike Liu, Longgen Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title | Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title_full | Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title_fullStr | Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title_full_unstemmed | Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title_short | Construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
title_sort | construction and validation of a predictive model for hepatocellular carcinoma based on serum markers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472335/ https://www.ncbi.nlm.nih.gov/pubmed/36100887 http://dx.doi.org/10.1186/s12876-022-02489-2 |
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