Evidence map›Paper›PMID 41122653›Full record

ArticleFrontiers in oncology2025

Prognostic value of LODDS in late-onset gastric adenocarcinoma: analysis of SEER, TCGA, and external multicenter cohorts.

Hengbo Xia, Yong Qian, Qingqing Pang, Aman Xu, Jie Hu

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Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 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.

Hengbo Xia *Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yong Qian *Department of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Qingqing Pang *Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Aman XuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Jie HuDepartment of Gastrointestinal Surgery, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Accurate survival prediction is crucial for optimizing individualized treatment and follow-up in patients with late-onset gastric adenocarcinoma (LOGA). Traditional lymph node staging systems such as N-stage, positive lymph node (PLN), and lymph node ratio (LNR) have limitations in predictive accuracy, especially in cases with inadequate lymph node dissection. The log odds of positive lymph nodes (LODDS), a novel nodal staging metric that incorporates both positive and negative lymph nodes through a log-transformed ratio, has shown potential advantages by providing a more stable and refined assessment of nodal involvement. Materials and methods: This study included 10,361 LOGA patients from the SEER database, 135 from TCGA, and 252 from two medical centers. A novel prognostic model was constructed based on a training cohort from SEER and validated using internal (SEER testing set) and external (TCGA and hospital datasets) cohorts. The model incorporated age, gender, grade, size, chemotherapy, and LODDS. Four staging systems (TNM-stage, PLN-stage, LNR-stage, LODDS-stage) were compared using the Akaike Information Criterion (AIC), Concordance Index (C-index) and time-dependent Area Under the Curve (AUC). LODDS-stage model, the most effective model, was used to build nomograms for overall survival (OS) and cause-specific survival (CSS). Model performance was evaluated using calibration curves, Decision Curve Analysis (DCA), and Kaplan-Meier analysis. Results: Univariate and multivariate Cox regression identified age, gender, grade, tumor size, chemotherapy, and LODDS-stage as independent prognostic factors. Among the four models, the LODDS-based model showed the highest discrimination and best calibration for predicting OS and CSS at 1, 3, 5, and 10 years. Nomograms incorporating these variables exhibited excellent predictive accuracy in both internal and external cohorts. Survival risk classification based on model scores effectively stratified patients into high- and low-risk groups, with significantly different survival outcomes across all datasets (p < 0.05). Conclusions: The LODDS-based prognostic model outperformed traditional nodal staging systems in survival prediction for LOGA patients. This model showed high accuracy and consistent performance across different datasets, indicating its potential to support personalized treatment and long-term follow-up strategies for elderly patients with gastric cancer.

Indexed as

cause-specific survivallate-onset gastric adenocarcinomaLODDSoverall survivalprognostic model

Identifiers

PMID41122653
PMCPMC12535910

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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.