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Feasibility study of S-1 for adjuvant chemotherapy in Biliary-Pancreatic cancer

Feasibility study of S-1 for adjuvant chemotherapy in Biliary-Pancreatic cancer - Feasibility study of S-1 for adjuvant chemotherapy in Biliary-Pancreatic cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004922
Enrollment
25
Registered
2013-03-01
Start date
2010-03-05
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

Biliary-Pancreatic cancer

Interventions

S-1 was administered orally after meals. The dosage of S-1 was 80mg/m2/day. S-1 is administred for 4 weeks followed by a 2-week rest. The administration of S-1 is continued for 1 year.

Sponsors

Osaka City University Graduate School of Medicine,Department of Hepato-Biliary-Pancreatic Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)pathologically diagnosed biliary or pancreatic cancer 2)pathologically curative resection 3)stage2,3,4 in Japanese Classification of Biliary or Pancreatic Carcinoma 4)no cancerous ascites and diatal metastasis 5)good oral intake 6)PS 0 or 1 (ECOG) 7)no previous chemotherapy or radiation in 3 years 8)administration of S-1 within 10 weeks after surgery 9)preserved organ function (bone marrow, liver,and kidney)

Exclusion criteria

Exclusion criteria: 1)previous treatment of S-1 2)recurrent case 3)fibroid lung or interstitial lung disease 4)active infectiou disease (excluding viral hepatitis) 5)sever complication 6)moderate ascites or pleural effusion 7)double cancer

Design outcomes

Primary

MeasureTime frame
Feasibility

Countries

Japan

Contacts

Public ContactHiroji Shinkawa

Osaka City University Department of Hepato-Biliary-Pancreatic Surgery

m1297198@msic.med.osaka-cu.ac.jp+81666453841

Outcome results

None listed

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