A machine learning clinic scoring system for hepatocellular carcinoma based on the Surveillance, Epidemiology, and End Results database.

Hepatocellular carcinoma (HCC) cancer-specific survival (CSS) machine learning (ML) risk stratification scoring system

Journal

Journal of gastrointestinal oncology
ISSN: 2078-6891
Titre abrégé: J Gastrointest Oncol
Pays: China
ID NLM: 101557751

Informations de publication

Date de publication:
30 Jun 2024
Historique:
received: 30 03 2024
accepted: 07 05 2024
medline: 11 7 2024
pubmed: 11 7 2024
entrez: 11 7 2024
Statut: ppublish

Résumé

Hepatocellular carcinoma (HCC) poses a global threat to life; however, numerical tools to predict the clinical prognosis of these patients remain scarce. The primary objective of this study is to establish a clinical scoring system for evaluating the overall survival (OS) rate and cancer-specific survival (CSS) rate in HCC patients. From the Surveillance, Epidemiology, and End Results (SEER) Program, we identified 45,827 primary HCC patients. These cases were randomly allocated to a training cohort (22,914 patients) and a validation cohort (22,913 patients). Univariate and multivariate Cox regression analyses, coupled with Kaplan-Meier methods, were employed to evaluate prognosis-related clinical and demographic features. Factors demonstrating prognostic significance were used to construct the model. The model's stability and accuracy were assessed through C-index, receiver operating characteristic (ROC) curves, calibration curves, and clinical decision curve analysis (DCA), while comparisons were made with the American Joint Committee on Cancer (AJCC) staging. Ultimately, machine learning (ML) quantified the variables in the model to establish a clinical scoring system. Univariate and multivariate Cox regression analyses identified 11 demographic and clinical-pathological features as independent prognostic indicators for both CSS and OS using. Two models, each incorporating the 11 features, were developed, both of which demonstrated significant prognostic relevance. The C-index for predicting CSS and OS surpassed that of the AJCC staging system. The area under the curve (AUC) in time-dependent ROC consistently exceeded 0.74 in both the training and validation sets. Furthermore, internal and external calibration plots indicated that the model predictions aligned closely with observed outcomes. Additionally, DCA demonstrated the superiority of the model over the AJCC staging system, yielding greater clinical net benefit. Ultimately, the quantified clinical scoring system could efficiently discriminate between high and low-risk patients. A ML clinical scoring system trained on a large-scale dataset exhibits good predictive and risk stratification performance in the cohorts. Such a clinical scoring system is readily integrable into clinical practice and will be valuable in enhancing the accuracy and efficiency of HCC management.

Sections du résumé

Background UNASSIGNED
Hepatocellular carcinoma (HCC) poses a global threat to life; however, numerical tools to predict the clinical prognosis of these patients remain scarce. The primary objective of this study is to establish a clinical scoring system for evaluating the overall survival (OS) rate and cancer-specific survival (CSS) rate in HCC patients.
Methods UNASSIGNED
From the Surveillance, Epidemiology, and End Results (SEER) Program, we identified 45,827 primary HCC patients. These cases were randomly allocated to a training cohort (22,914 patients) and a validation cohort (22,913 patients). Univariate and multivariate Cox regression analyses, coupled with Kaplan-Meier methods, were employed to evaluate prognosis-related clinical and demographic features. Factors demonstrating prognostic significance were used to construct the model. The model's stability and accuracy were assessed through C-index, receiver operating characteristic (ROC) curves, calibration curves, and clinical decision curve analysis (DCA), while comparisons were made with the American Joint Committee on Cancer (AJCC) staging. Ultimately, machine learning (ML) quantified the variables in the model to establish a clinical scoring system.
Results UNASSIGNED
Univariate and multivariate Cox regression analyses identified 11 demographic and clinical-pathological features as independent prognostic indicators for both CSS and OS using. Two models, each incorporating the 11 features, were developed, both of which demonstrated significant prognostic relevance. The C-index for predicting CSS and OS surpassed that of the AJCC staging system. The area under the curve (AUC) in time-dependent ROC consistently exceeded 0.74 in both the training and validation sets. Furthermore, internal and external calibration plots indicated that the model predictions aligned closely with observed outcomes. Additionally, DCA demonstrated the superiority of the model over the AJCC staging system, yielding greater clinical net benefit. Ultimately, the quantified clinical scoring system could efficiently discriminate between high and low-risk patients.
Conclusions UNASSIGNED
A ML clinical scoring system trained on a large-scale dataset exhibits good predictive and risk stratification performance in the cohorts. Such a clinical scoring system is readily integrable into clinical practice and will be valuable in enhancing the accuracy and efficiency of HCC management.

Identifiants

pubmed: 38989413
doi: 10.21037/jgo-24-230
pii: jgo-15-03-1082
pmc: PMC11231840
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1082-1100

Informations de copyright

2024 Journal of Gastrointestinal Oncology. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://jgo.amegroups.com/article/view/10.21037/jgo-24-230/coif). The authors have no conflicts of interest to declare.

Auteurs

Yueqing Wu (Y)

Department of General Surgery, The Fifth Affiliated Hospital of Zunyi Medical University, Zhuhai, China.

Chenyi Zhuo (C)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Yuan Lu (Y)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Zongjiang Luo (Z)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Libai Lu (L)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Jianchu Wang (J)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Qianli Tang (Q)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Meaghan M Phipps (MM)

Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.

William J Nahm (WJ)

New York University Grossman School of Medicine, New York, NY, USA.

Antonio Facciorusso (A)

Gastroenterology Unit, Department of Medical Sciences, University of Foggia, Foggia, Italy.

Bin Ge (B)

Department of Hepatobiliary and Pancreatic Surgery, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Guangxi Clinical Medical Research Center for Hepatobiliary Diseases, Baise, China.
Key Laboratory of Research on Prevention and Control of High Incidence Disease in Western Guangxi, Baise, China.

Classifications MeSH