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
| Type | Name | Description |
|---|---|---|
| DRUG | SOX plus PD-1 inhibitor | SOX or XELOX plus PD-1 inhibitor |
| DRUG | PD-1 / PD-L1 monoclonal antibody | PD-1/PD-L1 monoclonal antibody |
| DRUG | SOX Chemotherapy | SOX or XELOX |
| DRUG | Tegafur-Ugotex or Capecitabine | Tegafur-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.