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Feasibility and efficacy of preoperative chemoradiation and postoperative liver perfusion chemotherapy for T3 (UICC) pancreatic cancer

Feasibility and efficacy of preoperative chemoradiation and postoperative liver perfusion chemotherapy for T3 (UICC) pancreatic cancer - Pre- and post- operative adjuvant therapy for pancreatic cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001804
Enrollment
300
Registered
2009-03-27
Start date
2002-05-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic cancer

Interventions

Chemoradiation EXRT 50Gy gemcitabine 1000mg/m2 Liver perfusion chemotherapy 5FU 125mg/day via hepatic artery, 125mg/day via portal vein for 4 weeks (continuous infusion) or gemcitabine 1g via porta

Sponsors

Osaka Medical Center for cancer & Cardiovascular Diseases gastrointestinal & hepatobiliary- pancreatic surger
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Pancreatic cancer ; T3 of UICC TNM classification of malignant tumours 6th edition) Histological or cytological confirmation as pancreatic adenocarcinoma Performance status (ECOG) is 0 or 1

Exclusion criteria

Exclusion criteria: unusual running of hepatic artery, renal dysfunction, sever coronary disease, past history of malignant disease or chronic hepatitis, white blood cell count<3000/mm3, platelet count <104/mm3, Activated partial thromboplastin>50sec, ALT,AST>100U/l creatinine>1.5mg/dl

Design outcomes

Primary

MeasureTime frame
safety, survival

Secondary

MeasureTime frame
pathological response, pattern of failure

Countries

Japan

Contacts

Public ContactHiroaki Ohigashi

Osaka Medical Center for cancer & Cardiovascular Diseases gastrointestinal & hepatobiliary- pancreatic surgery

06-6972-1181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026