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Phase II study of neo-adjuvant chemotherapy with combination therapy of gemcitabine and S-1 in patients with resectable pancreatic cancer

Phase II study of neo-adjuvant chemotherapy with combination therapy of gemcitabine and S-1 in patients with resectable pancreatic cancer - PK-NACGS PhaseII

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005912
Enrollment
50
Registered
2011-07-03
Start date
2011-07-01
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

resectable pancreatic cancer

Interventions

Gemcitabine(1000mg/m2) is given by intravenous infusion over 30 min on day1, 8. S-1(65mg/m2) is given oral for 14 days followed by a 1-week rest. This cycle was repeated twice.

Sponsors

Tokai university, school of medicine
Lead Sponsor
Tokai University Hachioji Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)resectable or borderline resectable pancreatic cancer 2)sytologically or histrogically proven pancreatic invasive ductal cancer 3)all adult who anticipate to undergo pancreatectomy 4)Eastern Cooperative Oncology Group performance status of 0-1 5)adequate oral intake 6)adequate organ function 7)written informed consent

Exclusion criteria

Exclusion criteria: 1)pulmonary fibrosis or interstitional pneumonaitis 2)prior anti-cancer therapy(chemotherapy,radiation therapy ,chemoradiation therapy) 3)active infection 4)syncronous cancers 5)severe complication 6)severe mental disorder 7)watery diarrhea 8)pregnancy 9)iodine allergy

Design outcomes

Primary

MeasureTime frame
R0 resection rate

Secondary

MeasureTime frame
resection rate, adverse effect, completion rate, recurrence free survival, two-year survival rate, pathological effect

Countries

Japan

Outcome results

None listed

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