Evidence map›Paper›PMID 40074824›Full record

ArticleScientific reports2025

Study on the predictive value of preoperative CT features for the mitotic index of GIST based on the nomogram.

Ren Yingzheng, Jiang Linlin, Yang Yang, An Junjie, Dong Yonghong

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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 3 papers.

0numbers the graph read from it
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3citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ren YingzhengDepartment of Gastroenteropancreatic & Hernia Surgery, Shanxi Provincial People's Hospital, Shanxi Medical University, Shanxi, 030012, China.
Jiang LinlinDepartment of Gastroenteropancreatic & Hernia Surgery, Shanxi Provincial People's Hospital, Shanxi Medical University, Shanxi, 030012, China.
Yang YangDepartment of Gastroenteropancreatic & Hernia Surgery, Shanxi Provincial People's Hospital, Shanxi Medical University, Shanxi, 030012, China.
An JunjieDepartment of Gastroenteropancreatic & Hernia Surgery, Shanxi Provincial People's Hospital, Shanxi Medical University, Shanxi, 030012, China.
Dong YonghongDepartment of Gastroenteropancreatic & Hernia Surgery, Shanxi Provincial People's Hospital, Shanxi Medical University, Shanxi, 030012, China. youthdong007@163.com.

Funding

Wu Jieping Medical Foundation 320.6750.2022-3-41
6 · The paper itself

Abstract

This study aimed to construct a Nomogram based on preoperative CT features to predict the mitotic index in gastrointestinal stromal tumors and to establish preoperative risk stratification. The constructed nomogram prediction model is targeted towards guiding preoperative risk stratification, facilitating the provision of rational drug administration regimens, and tailoring appropriate surgical plans for personalized treatment. The imaging and pathological data of 250 patients with gastrointestinal stromal tumors in Shanxi Provincial hospital from January 2019 to January 2024 were retrospectively analyzed. According to the pathological data, the patients were divided into high mitotic index and low mitotic index, and were divided into a training group (n = 176) and a validation group (n = 74) according to a stratified sampling ratio of 7:3. In the training group, statistically significant variables were screened out by univariate analysis for multivariate logistic regression analysis, and independent risk factors were screened out and a Nomogram prediction model was constructed. The receiver operating characteristic (ROC) was used to evaluate the model discrimination, and the predicted probability risk was stratified by the optimal cutoff value. The Hosmer-Lemeshow test (HL test) was performed, and the calibration curve was drawn by Bootstrap repeated sampling 1000 times to evaluate the model consistency. Finally, the clinical application value of the prediction model was evaluated by the decision curve analysis (DCA). There were no significant differences in the distribution of clinical characteristics and CT features between the training group and the validation group ( P>0.05). Univariate analysis showed that the differences in tumor size, tumor site, boundary, calcification, liquefaction/necrosis, morphological characteristics, growth pattern, and ulceration were statistically significant (P<0.05). Multivariate logistic regression analysis screened out tumor size (GIST ≤ 2 cm, P = 0.018; GIST 2-5 cm, p = 0.009; GIST 5-10 cm, P = 0.017), liquefaction/necrosis (P = 0.002), and morphological characteristics (P = 0.002) as independent risk factors for high mitotic index. The Nomogram was established based on these three factors. The area under the curve (AUC) of the training group and the validation group of the model were 0.851 (95%CI: 0.793-0.91) and 0.836 (95%CI: 0.735-0.937), the specificity was 0.696 and 0.735, and the sensitivity was 0.869 and 0.760, respectively. The HL test had good calibration (training group P = 0.461, validation group P = 0.822), indicating that the predicted risk was consistent with the actual risk. The DCA also showed good clinical practicality. The Nomogram prediction model that incorporates preoperative CT features of tumor size, liquefaction/necrosis, and morphological characteristics can effectively predict the number of mitotic figures in gastrointestinal stromal tumors, and can perform effective preoperative risk stratification to guide clinical decision-making and personalized treatment.

Indexed as

Gastrointestinal NeoplasmsGastrointestinal Stromal TumorsMitotic IndexNomogramsTomography, X-Ray ComputedAdultAgedFemaleHumansMaleMiddle AgedPredictive Value of TestsRetrospective StudiesRisk AssessmentRisk FactorsROC CurveCT featuresGastrointestinal stromal tumorMitotic indexPrediction model

Identifiers

PMID40074824
PMCPMC11904199

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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.