Evidence map›Paper›PMID 42047496›Full record

Observational studyJournal of digestive diseases

Development and Validation of an Individualized Nomogram to Identify Undifferentiated-Predominant Mixed-Type Early Gastric Cancer.

Lin Lin Shao, Yu Miao Zheng, Qian Zhang, Chuan Guo Guo, Peng Li

Abstract readObservational StudyValidation Study
In one paragraph

Observational study in Journal of digestive diseases. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lin Lin ShaoDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0002-8794-907X
Yu Miao ZhengDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Qian ZhangDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Chuan Guo GuoDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Peng LiDepartment of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0003-2927-2758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDiagnosis of undifferentiated-type-predominant mixed-type early gastric cancer (UM-EGC) remains challenging due to its complex histological features and overlapping characteristics with other gastric cancer types. We aimed to develop a novel nomogram based on clinicopathological and endoscopic features and validate its performance in predicting UM-EGC prior to endoscopic treatment.

methodsIn this retrospective single-center study, 808 patients with early gastric cancer (EGC) who underwent curative endoscopic submucosal dissection were included. Among them, 493 were assigned to the training cohort and 84 to the external validation cohort. Clinicopathological characteristics and endoscopic features were compared between differentiated EGC and UM-EGC using logistic regression analysis. A predictive nomogram was constructed and evaluated.

resultsMultivariable regression analysis identified open-type atrophic gastritis (O1-O3) (odds ratio [OR] 0.25, 95% confidence interval [CI] 0.08-0.82), IIb (OR 9.72, 95% CI 3.01-31.35), IIc (OR 7.75, 95% CI 2.81-21.39), discolored lesion (OR 4.12, 95% CI 1.57-10.80), horizontal location at the greater curvature (OR 2.98, 95% CI 1.15-7.75) or anterior wall (OR 2.91, 95% CI 1.26-6.74), and previous H. pylori eradication (OR 0.23, 95% CI 0.09-0.55) as independently associated with UM-EGC. UM-EGC was also more susceptible to metachronous cancer (OR 5.50, 95% CI 1.30-23.21). The nomogram demonstrated good discriminative ability with an area under the receiver operating characteristic curve of 0.83 (95% CI 0.77-0.87) in the training cohort and 0.82 (95% CI 0.69-0.98) in the external validation cohort.

conclusionThis nomogram comprising clinicopathological and endoscopic features may assist in the preoperative prediction of UM-EGC risk.

trial registrationThe clinical trial registration number for patient source in this study is ChiCTR1800017117.

Indexed as

NomogramsStomach NeoplasmsAgedEarly Detection of CancerEndoscopic Mucosal ResectionFemaleGastroscopyHumansMaleMiddle AgedRetrospective Studiesclinicopathological featureendoscopic featureHelicobacter pylorinomogramundifferentiated‐type‐predominant mixed‐type early gastric cancer

Identifiers

PMID42047496
PMCPMC13281755

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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.