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

120 Participants
are divided into 2 treatment groups

Locations

1
Bakirkoy Dr. Sadi Konuk Training and Research Hospital34147, IstanbulIstanbul, Turkey (Türkiye)

Sponsors 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