The Clinical Efficacy of Drug Sensitive Neoadjuvant Chemotherapy Based on Organoid Versus Traditional Neoadjuvant Chemotherapy in Advanced Gastric Cancer
NCT05351398 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 54
Last updated 2022-04-28
Summary
Neoadjuvant chemotherapy has become the mainstream recommended treatment for advanced gastric cancer. However, due to the heterogeneity of gastric cancer, part of some patients fail to benefit from the treatment. This project aims to compare the clinical efficacy of individualized neoadjuvant therapy based on patient-derived organoid drug sensitivity assay and traditional regimen, exploring the advantages and disadvantages of these two treatments. And access the safety and clinical value of the personalized neoadjuvant therapy based on patient-derived organoid drug sensitivity assay in advanced gastric cancer.
Conditions
- Advanced Gastric Carcinoma
Interventions
- DRUG
-
PDO group
Patients with stage III gastric cancer who need neoadjuvant chemotherapy before radical surgery are recruited. And they are treated with individualized neoadjuvant therapy under the guidance of a patient-derived organoid (PDO)-based drug sensitivity assay.
- DRUG
-
Traditional group
Patients with stage III gastric cancer who need neoadjuvant chemotherapy before radical surgery are recruited. In this group, patients are treated with the SOX regimen.
Sponsors & Collaborators
-
Ruijin Hospital
collaborator OTHER -
Shanghai OneTar Biomedicine Co., Ltd.
collaborator UNKNOWN -
Shanghai Minimally Invasive Surgery Center
lead OTHER
Principal Investigators
-
Jing Sun, PhD · Shanghai Jiao Tong University School of Medicine
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-04-30
- Primary Completion
- 2023-06-30
- Completion
- 2023-12-31
Countries
- China
Study Locations
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