Proximal Gastrectomy vs Total Gastrectomy in Locally Advanced Upper Gastric Cancer After Neoadjuvant Therapy

NCT06597227 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 404

Last updated 2026-04-27

No results posted yet for this study

Summary

We plan to evaluate the efficacy and safety of proximal gastric vs. total gastric radical resection after SOX combined with anti-PD-1 neoadjuvant therapy in locally advanced upper gastric cancer

Conditions

  • Locally Advanced Gastric Cancer

Interventions

PROCEDURE

Total radical gastrectomy

total radical gastrectomy : Dissection of lymph nodes No.1-7, 8a, 9, 11p, 11d, 12a are recommended. The tumor involved more than 3cm of esophagus and additional dissection No.19, 20, 110. Gastrointestinal reconstruction method: Roux⁃en⁃Y anastomosis is recommended

PROCEDURE

Proximal radical gastrectomy

Proximal radical gastrectomy : Dissection of lymph nodes No.1,2,3a,4sa,4sb,7,8a, 9, 11p, 11dare recommended. The tumor involved more than 3cm of esophagus and additional dissection No.19, 20, 110. Gastrointestinal reconstruction method: double channel anastomosis is recommended, and other anastomosis methods can be carried out according to the surgeon\'s habit.

Sponsors & Collaborators

  • Fudan University

    collaborator OTHER
  • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

    collaborator OTHER
  • Xiangya Hospital of Central South University

    collaborator OTHER
  • Shandong First Medical University

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • The First Medical Center of Chinese PLA General Hospital

    collaborator OTHER
  • Affiliated Hospital of Qinghai University

    collaborator OTHER
  • Qilu Hospital of Shandong University

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • First Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Southern Medical University, China

    collaborator OTHER
  • Shanxi Bethune Hospital

    collaborator OTHER
  • The First Affiliated Hospital of Zhengzhou University

    collaborator OTHER
  • The Third Xiangya Hospital of Central South University

    collaborator OTHER
  • Jingzhou Central Hospital

    collaborator OTHER
  • Xiangyang Central Hospital

    collaborator OTHER
  • Yichang Central People's Hospital

    collaborator OTHER
  • The First Affiliated Hospital of University of South China

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • People's Hospital of Macheng City

    collaborator UNKNOWN
  • Southwest Hospital, China

    collaborator OTHER
  • Liaoning Cancer Hospital & Institute

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Changhai Hospital

    collaborator OTHER
  • The First Affilated Hospital of the Medical College, Shihezi University

    collaborator OTHER
  • First Affiliated Hospital Xi'an Jiaotong University

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • First Hospital of China Medical University

    collaborator OTHER
  • Shanghai East Hospital

    collaborator OTHER
  • General Hospital of Ningxia Medical University

    collaborator OTHER
  • Shanghai Changzheng Hospital

    collaborator OTHER
  • Guihua Wang

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2026-12-30
Completion
2028-12-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06597227 on ClinicalTrials.gov