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Integrating Multi-Omics Data for Enhanced Prognosis Prediction in Gastric Cancer Post-Neoadjuvant Therapy

Integrating Multi-Omics Data for Enhanced Prognosis Prediction in Gastric Cancer Post-Neoadjuvant Therapy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07190040
Enrollment
179
Registered
2025-09-24
Start date
2019-01-01
Completion date
2025-09-01
Last updated
2025-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric Cancer (GC)

Brief summary

Study Protocol: Integrating Multi-Omics Data for Prognosis Prediction in Gastric Cancer Post-Neoadjuvant Therapy Objective: To develop and validate an integrative prognostic nomogram for patients with locally advanced gastric cancer (LAGC) undergoing neoadjuvant therapy, combining deep learning-derived radiomic features (DeepScore), transcriptome-based immune scores (ImmuneScore), and ypTNM staging. Study Design: A retrospective, single-center cohort study. Participants: A total of 179 LAGC patients who received neoadjuvant therapy followed by radical gastrectomy at Fujian Medical University Union Hospital between January 2019 and December 2022. Patients were divided into a training cohort (n = 125) and an independent validation cohort (n = 54). Data Collection: Baseline contrast-enhanced CT scans prior to neoadjuvant therapy were used for radiomic analysis. Postoperative tumor RNA sequencing data were used for immune profiling. Clinical and pathological data, including ypTNM stage, were collected from medical records. Methods: DeepScore: Extracted from CT images using a ResNet18-based deep learning model. Significant features were selected via univariate Cox and LASSO regression. ImmuneScore: Calculated from RNA-seq data using the ESTIMATE algorithm to assess tumor immune infiltration. Nomogram Construction: A multi-omics nomogram was developed using multivariate Cox regression incorporating DeepScore, ImmuneScore, and ypTNM stage. Validation: Model performance was evaluated using time-dependent ROC analysis (AUC) and Kaplan-Meier survival analysis with log-rank tests in both cohorts. Primary Outcomes: Disease-free survival (DFS) and overall survival (OS). Statistical Analysis: Survival analyses were performed using Kaplan-Meier and Cox regression models. AUC values were computed for 1-, 2-, and 3-year DFS predictions. All analyses were conducted in R (v4.4.3).

Interventions

None listed

Sponsors

Chang-Ming Huang, Prof.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Gastric adenocarcinoma confirmed pathologically via gastroscopy; * Clinical staging of cT3/T4N0/+M0 with a history of receiving at least two cycles of neoadjuvant therapy * No prior history of other malignant tumors * Completion of radical gastrectomy

Exclusion criteria

* Gastric cancer originating from the remnant stomach * Absence of baseline computed tomography (CT) data prior to treatment or suboptimal CT image quality that could compromise the accuracy of radiomic information extraction * Absence of postoperative transcriptome data

Design outcomes

Primary

MeasureTime frameDescription
the Area Under the Curve2023.01.31-2025.05.31The model's predictive accuracy was evaluated by computing the Area Under the Curve for predicting 1-year, 2-year, and 3-year disease-free survival.

Secondary

MeasureTime frameDescription
Disease-free survival2023.01.31-2025.05.31The log-rank test was utilized to compare disease-free survival and overall survival curves between these groups.

Other

MeasureTime frameDescription
Overall survival2023.01.31-2025.05.31The log-rank test was utilized to compare disease-free survival and overall survival curves between these groups.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026