About this trial
This multicenter prospective randomized clinical trial aims to compare the safety and oncological effectiveness of proximal gastrectomy and total gastrectomy in patients with locally advanced Siewert type II-III gastroesophageal junction cancer. Eligible patients will be randomly assigned to undergo either proximal gastrectomy or total gastrectomy using open, laparoscopic, or robotic surgical approaches according to clinical suitability. The primary outcome of the study is 3-year disease-free survival. Secondary outcomes include postoperative mortality, postoperative complications, and the number of metastatic lymph nodes retrieved. Patients will be followed for up to five years after surgery to evaluate long-term oncological outcomes.
Eligibility criteria
Qualifiers
Age between 18 and 90 years
Histologically confirmed locally advanced Siewert type II-III gastroesophageal junction cancer
Considered operable after multidisciplinary tumor board evaluation
Candidate for curative surgical resection with D2 lymphadenectomy
Disqualifiers
Early-stage gastroesophageal junction cancer
Gastric cancers located in the antrum or corpus
Severe anesthetic risk (American Society of Anesthesiologists [ASA] class IV or higher)
Pregnancy
Trial design
Treatments tested in this trial
- Proximal Gastrectomy
- Total Gastrectomy
Treatment groups
Locations
1Sponsors and collaborators
Nurettin Şahin
Lead sponsor
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Sponsor institution
Ankara City Hospital Bilkent
Collaborator
Bakirkoy Dr. Sadi Konuk Research and Training Hospital
Collaborator
Istanbul University - Cerrahpasa
Collaborator