Eligibility included histologically proven resectable (R) or borderline resectable (BR) pancreatic ductal adenocarcinoma with contact of SMV/PV. Exclusion criteria was liver/lung metastasis, para-aortic lymph node metastasis positive or peritoneal metastasis.
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Eligibility included histologically proven resectable (R) or borderline resectable (BR) pancreatic ductal adenocarcinoma with contact of SMV/PV.
Exclusion criteria
Exclusion criteria: Exclusion criteria was lung and liver metastasis, para-aortic lymph node metastasis positive, lavage cytology positive or peritoneal metastasis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint was feasibility rate of preoperative planned portal vein resection. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint was safety including operative outcomes (duration of surgery, blood loss and transfusion) and postoperative outcomes (in-hospital mortality and morbidity, pathological findings, patency rate of portal vein). | — |
Countries
Japan
Contacts
Juntendo University School of Medicine Department of Hepatobiliary-Pancreatic Surgery