Evidence map›Paper›PMID 40713513›Full record

ArticleBMC cancer2025

Identification of gastroenteropancreatic neuroendocrine tumor patients with high liver tumor burden based on clinicopathological features.

Nuerailaguli Jumai, Luohai Chen, Xiaoxuan Lin, Qiao He, Man Liu, Yuan Lin, Yanji Luo, Yu Wang, Min-Hu Chen, Xiangsong Zhang and 2 more

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Nuerailaguli JumaiDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Luohai ChenDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiaoxuan LinDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Qiao HeDepartment of Nuclear Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Man LiuDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yuan LinDepartment of Pathology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yanji LuoDepartment of Radiology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yu WangDepartment of Interventional Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Min-Hu ChenDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiangsong ZhangDepartment of Nuclear Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Zhirong ZengDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Ning ZhangDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China. zhangn5@mail.sysu.edu.cn.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2021A1515110241China Postdoctoral Science Foundation 2022M723602
6 · The paper itself

Abstract

backgroundMetastatic liver tumor burden (LTB) is a prognostic factor affecting the survival of gastroenteropancreatic neuroendocrine tumors (GEP-NETs), but evaluation of the LTB usually depends on radiologic and functional imaging. This study aimed to develop a clinical model based on easily accessible clinicopathological markers to predict LTB level in GEP-NET patients.

methodsLTB was quantified based on 68Ga-DOTANOC PET/CT scan. The optimal cut-off value for high and low-LTB was determined based on our previous study. Serum levels of liver enzymes and tumor biomarkers were obtained within one week before PET/CT scan. The whole dataset was divided into training set and validation set. LASSO regression method was used to select predictors, and multivariate logistic regression was used to develop a clinical model which was further visualized by constructing a nomogram. Area under the curve (AUC) was applied to assess the accuracy of the constructed model.

resultsWe retrospectively enrolled 200 patients with well-differentiated GEP-NETs. Ki-67 index, GGT (gamma-glutamyltransferase), LDH (lactate dehydrogenase), and NSE (neuron-specific enolase) were selected through the LASSO regression method, and a nomogram was built based on these variables. The predictive model yielded an AUC of 0.785 (95% CI, [0.708–0.862]) in the training set, and 0.783 (95% CI, [0.644–0.923]) in the validation set. Additionally, with the optimal cut-off values based on the nomogram total points, patients were categorized as LTBhigh (total points ≥ 26.2) and LTBlow (total points < 26.2) groups presenting significantly different OS.

conclusionA clinically applicable nomogram incorporating four clinicopathological characteristics was constructed to predict GEP-NET patients with high-LTB. The nomogram may help clinicians identify patients with high-LTB and take optimal treatment measures to improve prognosis.

Indexed as

Intestinal NeoplasmsLiver NeoplasmsNeuroendocrine TumorsPancreatic NeoplasmsStomach NeoplasmsAdultAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedNomogramsPositron Emission Tomography Computed TomographyPrognosisRetrospective StudiesBiomarkers, TumorLiver metastasisNeuroendocrine tumorsPrognosisTumor burden

Identifiers

PMID40713513
PMCPMC12297730

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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.