ArticleClinical & experimental metastasis2026
A novel multimodal combining radiomics and tumor-stroma ratio (TSR) improves diagnosis of gastric cancer peritoneal metastasis.
Article in Clinical & experimental metastasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
Peritoneal metastasis (PM) is the most common form of metastasis in gastric cancer (GC), frequently leading to severe complications and a significantly poor prognosis. Prompt and early diagnosis of PM in GC is crucial. However, diagnostic laparoscopy and CT scans, while being the primary methods for identifying PM in GC, have notable limitations, such as being invasive and having low sensitivity. Therefore, developing a diagnostic model for PM in GC based on routine examination results holds substantial importance. In this retrospective study, we enrolled 813 patients from two medical centers and developed a robust diagnostic model by integrating various routine examination results, including CT scans, endoscopy, pathology, and hematological tests. To further explore the potential significance of various examination results, we conducted radiomic analysis of CT images, analyzed histopathological results via the Tumor-Stroma Ratio (TSR), and examined hematological results through parameters such as the Prognostic Nutritional Index (PNI), Neutrophil to Lymphocyte Ratio (NLR), and Albumin to Globulin Ratio (AGR). A novel diagnostic model, incorporating CA125, CA724, Borrmann classification, radiomics features, and the TSR, was successfully constructed. This model demonstrated strong performance in diagnosing synchronous PM (AUC = 0.874) and predicting metachronous (AUC = 0.784) PM in GC. To facilitate clinical application, a nomogram was constructed. Consequently, the study presents a novel and comprehensive diagnostic model for PM in GC patients, offering significant promise for clinical applicability based on routine examination results.
Indexed as
Identifiers
41714437What Socratic holds
Registered trials
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 Socratic graph.