Evidence map›Paper›PMID 40998994›Full record

ArticleScientific reports2025

A nomogram and random forest model for predicting liver metastasis in patients with early-onset colorectal cancer.

Xingzhi Han, Xueying Bai, Qun Zhang, Xiaoping Qian

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Xingzhi HanDepartment of Comprehensive Cancer Centre, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, 321 Zhong Shan Rd, Nanjing, 210008, People's Republic of China.
Xueying BaiNanjing Drum Tower Hospital Clinical College of Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Qun ZhangComprehensive Cancer Centre of Nanjing Drum Tower Hospital, Medical School of Nanjing University, Clinical Cancer Institute of Nanjing University, 321 Zhong Shan Rd, Nanjing, 210008, People's Republic of China. qunzhangnora@outlook.com.ORCID http://orcid.org/0000-0001-6013-317X
Xiaoping QianDepartment of Comprehensive Cancer Centre, Affiliated Hospital of Medical School, Nanjing Drum Tower Hospital, Nanjing University, 321 Zhong Shan Rd, Nanjing, 210008, People's Republic of China. xiaopingqian@nju.edu.cn.ORCID http://orcid.org/0000-0002-5025-5269

Funding

Jiangsu Scientific and Technological Development of Traditional Chinese Medicine Key projects ZD202227Nanjing Health Science and Technology Development Key Program ZKX21028National Natural Science Foundation of China 82303970Provincial Natural Science Foundation of Jiangsu BK20211007
6 · The paper itself

Abstract

The incidence of colorectal cancer (CRC) in individuals under the age of 50 has increased. Liver metastasis (LM) is the most common metastasis in CRC patients and is associated with a poor prognosis. This study aimed to use public databases to identify the risk factors for LM in early-onset colorectal cancer (EOCRC) patients and develop a nomogram to quantify the risk of LM. We retrospectively collected data of EOCRC patients diagnosed from 2010 to 2015 in the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate logistic analysis were used to screen and validate the risk factors for LM in EOCRC patients, and a nomogram was established based on these factors. Calibration curve, area under the receiver operating curve (AUC), and decision curve analysis (DCA) were developed to evaluate the accuracy of the model. A total of 2567 EOCRC patients were included and randomly divided into a training set (n = 1797) and a validation set (n = 770) at a ratio of 7:3. Univariate and multivariate analyses showed that N stage, pretreatment CEA, bone metastasis, and lung metastasis were independent risk factors. The AUCs of the training set and validation set were 0.7958 and 0.7653, respectively, and the calibration curve also demonstrated good accuracy and predictive ability. DCA indicated that it was more clinically relevant than the traditional TN staging. We constructed a Random Forest model, and calculated the SHapley Additive exPlanations (SHAP) values to determine variables importance and visualize the results. We developed a nomogram to predict the risk of LM in EOCRC patients, and the model was internally validated with good accuracy and reliability. It can assist doctors in risk assessment and clinical decision-making.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsNomogramsAdultAgedAge of OnsetFemaleHumansMaleMiddle AgedPrognosisRandom ForestRetrospective StudiesRisk FactorsROC CurveSEER ProgramColorectal cancerLiver metastasisNomogramSEER

Identifiers

PMID40998994
PMCPMC12464121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.