MedPath

Neoadjuvant Treatment Based on Gastric Cancer Molecular Subtyping.

Completed
Conditions
Advanced Gastric Cancer
Multi-omics Analysis
Neoadjuvant Therapy
Interventions
Procedure: combination chemotherapy with Apatinib or Camrelizumab
Registration Number
NCT06376773
Lead Sponsor
Fujian Medical University
Brief Summary

Extensive research employing diverse omics methodologies has unveiled a varied landscape of gastric cancer (GC). Recent progress in next-generation sequencing and other genomic technologies has facilitated a more intricate exploration of GC at the molecular level. This study aimed to identify the most effective drug therapeutics for patients with the mesenchymal subtype of gastric cancer.Based on RNA-seq transcriptome, 234 patients were divided into four molecular subtypes: mesenchymal, immunogenic, metabolic, and classic.Our analysis has revealed that, for neoadjuvant therapy in advanced gastric cancer (AGC), the mesenchymal subtype stands out as the ideal patient population benefiting from Apatinib, without a concurrent increase in postoperative complications.

Detailed Description

The advent of immunotherapy and targeted therapies has recently provided new options for AGC treatment. However, not all patients benefit from immunotherapy or targeted therapy, resulting in unsatisfactory overall treatment outcomes during the perioperative period. An ineffective treatment imposes significant financial burden, causes drug-related side effects that deteriorate their quality of life, and potentially delays subsequent treatment.

Evaluate the objective response rate (ORR) of the combination of camrelizumb, apatinib, and neoadjuvant chemotherapy for the treatment of advanced gastric patient Median survival time (OS);

Disease free survival time (DFS);

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
234
Inclusion Criteria
  • diagnosed with gastric adenocarcinoma and received neoadjuvant therapy
Exclusion Criteria
  • Patients with distant metastases, gastric stump cancer, or missing neoadjuvant chemotherapy data were excluded from the study.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
mesenchymalcombination chemotherapy with Apatinib or CamrelizumabBased on RNA-seq transcriptome, patients were divided into mesenchymal, and received neoadjuvant chemotherapy with apatinib or not
immunogeniccombination chemotherapy with Apatinib or CamrelizumabBased on RNA-seq transcriptome, patients were divided into immunogenic, and received neoadjuvant chemotherapy with Camrelizumab or not
Primary Outcome Measures
NameTimeMethod
overall survival2years

overall survival

Secondary Outcome Measures
NameTimeMethod
objective response rate6months

objective response rate

Trial Locations

Locations (1)

Fujian Medical University Union Hospital

🇨🇳

Fuzhou, Fujian, China

© Copyright 2025. All Rights Reserved by MedPath