Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07161453

Comparing the Efficacy and Safety of Different Postoperative Adjuvant Regimens in Patients With Resectable Adenocarcinoma of the Esophagogastric Junction Who Underwent Radical Surgery After Neoadjuvant Chemotherapy Combined With Immunotherapy and Achieved pCR in Postoperative Pathology

A Multicenter, Prospective, Real-world Study Comparing the Efficacy and Safety of Different Postoperative Adjuvant Regimens in Patients With Resectable Adenocarcinoma of the Esophagogastric Junction Who Underwent Radical Surgery After Neoadjuvant Chemotherapy Combined With Immunotherapy and Achieved pCR in Postoperative Pathology

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
500 (estimated)
Sponsor
Liaoning Cancer Hospital & Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is to evaluate the efficacy and safety of different postoperative adjuvant regimens in patients with resectable adenocarcinoma of the esophagogastric junction who underwent radical surgery after neoadjuvant chemotherapy combined with immunotherapy and achieved pCR in postoperative pathology

Conditions

Interventions

TypeNameDescription
DRUGSOX plus PD-1 inhibitorSOX or XELOX plus PD-1 inhibitor
DRUGPD-1 / PD-L1 monoclonal antibodyPD-1/PD-L1 monoclonal antibody
DRUGSOX ChemotherapySOX or XELOX
DRUGTegafur-Ugotex or CapecitabineTegafur-Ugotex or Capecitabine

Timeline

Start date
2025-09-30
Primary completion
2027-09-30
Completion
2027-12-31
First posted
2025-09-08
Last updated
2025-09-08

Source: ClinicalTrials.gov record NCT07161453. Inclusion in this directory is not an endorsement.