Evidence map›Paper›PMID 41174585›Full record

ArticleBMC surgery2025

Prognostic model for early gastric cardia cancer after endoscopic submucosal dissection.

Peng Zhang, Xiaoying Ma, Zibin Tian, Zheng Cui, Zhen Zhang, Tao Mao

Abstract read
In one paragraph

Article in BMC surgery, 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 · The record

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5 · Who and what money

Authors and funding

6 authors.

Peng ZhangDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao City, Shandong Province, 266000, China.
Xiaoying MaDepartment of Gastroenterology, Qingdao Municipal Hospital, Qingdao City, Shandong Province, China.
Zibin TianDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao City, Shandong Province, 266000, China.
Zheng CuiDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao City, Shandong Province, 266000, China.
Zhen ZhangDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao City, Shandong Province, 266000, China.
Tao MaoDepartment of Gastroenterology, The Affiliated Hospital of Qingdao University, No. 16 Jiangsu Road, Qingdao City, Shandong Province, 266000, China. sdf15674334@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo develop and validate a prognostic model incorporating microRNA-1246 (miR-1246), high-mobility group box 1 (HMGB-1), α1-antitrypsin (A1AT), and inflammatory markers for predicting outcomes in early gastric cardia cancer after endoscopic submucosal dissection (ESD).

methodsWe retrospectively enrolled 280 patients with early gastric cardia cancer who underwent ESD between January 2021 and December 2023. Patients were divided into a training set (n = 196) and a validation set (n = 84) at a ratio of 7:3. Influencing factors were screened using univariate, Least Absolute Shrinkage and Selection Operator (LASSO), and multivariate logistic regression analyses in the training set. A nomogram was constructed, and the predictive performance was assessed using receiver operating characteristic (ROC) curves and calibration curves. Decision curve analysis (DCA) was used to evaluate the clinical value.

resultsThe incidence of poor prognosis was comparable between training (43.88%) and validation set (34.52%). Multivariate logistic regression analysis identified miR-1246, HMGB-1, A1AT, tumor necrosis factor-α (TNF-α), and Helicobacter pylori infection as independent risk factors for poor prognosis (All P < 0.05). The nomogram demonstrated acceptable discriminative ability, with AUC of 0.789 (95% CI: 0.701-0.877) in the training set and 0.735 (95% CI: 0.638-0.835) in the validation set. The sensitivity and specificity were 0.625 and 0.841 for the training set, and 0.481 and 0.786 for the validation set, respectively. Calibration curves indicated good agreement between predicted and observed probabilities.

conclusionThe proposed prognostic model offers a practical tool for individualized risk assessment post-ESD. However, the clinical application warrants further validation in large-scale, multi-center prospective studies with long-term follow-up.

Indexed as

CardiaEndoscopic Mucosal ResectionStomach NeoplasmsAgedBiomarkers, TumorFemaleHMGB1 ProteinHumansMaleMicroRNAsMiddle AgedNomogramsPrognosisRetrospective StudiesRisk FactorsTumor Necrosis Factor-alphaBiomarkers, TumorHMGB1 ProteinHMGB1 protein, humanMicroRNAsTumor Necrosis Factor-alphaEarly gastric cardia cancerEndoscopic submucosal dissectionHigh mobility group box 1MicroRNA-1246Prognostic modelΑ1-antitrypsin

Identifiers

PMID41174585
PMCPMC12577123

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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.