Evidence map›Paper›PMID 39974390›Full record

ArticleTranslational cancer research2025

A predictive nomogram for predicting liver metastasis in early-onset colon cancer: a population-based study.

Weichao Zeng, Yafeng Sun, Zhengrong Liao, Jianhua Xu

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Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 authors.

Weichao ZengDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.ORCID https://orcid.org/0000-0002-0263-0976
Yafeng SunDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Zhengrong LiaoDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Jianhua XuDepartment of Gastrointestinal Surgery, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The risk of liver metastasis (LM) may be estimated using predictive nomograms. While the nomogram has recently been applied in oncology, there are relatively few studies concentrating on predicting LM in patients with early-onset colon cancer. We aimed to identify independent risk factors for LM in patients with early-onset colon cancer and develop a nomogram for predicting the probability of LM in these patients. Methods: Our study encompassed 4,890 early-onset colon cancer patients with LM who were registered in the Surveillance, Epidemiology, and End Results (SEER) database from 2010 to 2015. These patients were randomly allocated into training and validation cohorts at a ratio of 7:3. Univariate and multivariate logistic regression analyses were conducted to identify the independent risk factors for LM, and a nomogram was developed using these factors. The model's discriminatory power, accuracy, and clinical utility were evaluated using receiver operating characteristics (ROC), calibration, and decision curve analyses. Results: Overall, 4,890 patients with early-onset colon cancer and LM were selected from the SEER database. LM incidence in these patients was 18.4%. Univariate and multivariate analyses revealed histological type, T stage, N stage, and carcinoembryonic antigen (CEA) level as independent risk factors. ROC curve analysis revealed that the predictive nomogram for LM risk had an area under the curve of 0.812 [95% confidence interval (CI): 0.795-0.829] and 0.809 (95% CI: 0.784-0.834) in the training and validation sets, respectively, demonstrating good discriminatory ability of the model. Calibration curve analysis showed good agreement between predicted values from the nomogram and actual observations, and the decision curve analysis (DCA) demonstrated the high clinical utility of the nomogram. Conclusions: LM incidence was higher in patients with early-onset colon cancer. Our nomogram demonstrates a high level of efficacy in predicting the risk of LM in patients with early-onset colon cancer, thereby assisting clinicians in making well-informed treatment decisions prior to further intervention.

Indexed as

Early-onset colon cancerliver metastasis (LM)nomogramrisk factorsSurveillance, Epidemiology, and End Results database (SEER database)

Identifiers

PMID39974390
PMCPMC11833359

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