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Phase II study of surgical resection following neoadjuvant chemoradiation using Gemcitibine and TS-1 in patients with potentially and borderline resectable pancreatic cancer

Phase II study of surgical resection following neoadjuvant chemoradiation using Gemcitibine and TS-1 in patients with potentially and borderline resectable pancreatic cancer - Phase II study of surgical resection following neoadjuvant chemoradiation in pancreatic cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003629
Enrollment
30
Registered
2010-06-01
Start date
2010-06-01
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

potentially and borderline resectable pancreatic cancer

Interventions

To investigate the frequency of histological curative resection following chemoradiation using Gemcitabine and TS-1in patients with potentially resectable pancreatic cancer

Sponsors

Kansai Medical University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with Histo-cytologically confirmed pancreatic cancer 2.Patients who have not undergone chemo and/or radiotherapy 3.Patients with radiologically defined patentially resectable pancreatic cancer 4.Patients with no metastatic disease confirmed by staging laparoscopy 5.Patients with Performance status of 0/1 6.Patients with sustained organ function 7.Patients with potentially resectable pancreatic cancer by CT following neoadjuvant chemoradiation 8.Patients who received informed consent

Exclusion criteria

Exclusion criteria: 1) Patients with other active cancers 2) Patients with watery diarrhea 3) Intractable pleural and pericardical effusion, or ascites 4) Severe co-morbid diseases 5) Pregnancy or insufficient contraception 6) Past history of severe drug-allergy 7) Active bacterial or viral infection 8) younger than 20 years old or older than 90 years old. 9) No written informed consent of the patients 10) Pregnancy or insufficient contraception 11) HIV infection 12) Doubtful understanding or contractual capacity of the patient 13) Patients seems inadequate for this study by investigator(s)

Design outcomes

Primary

MeasureTime frame
frequency of radical resection (R0)

Countries

Japan

Contacts

Public ContactSohei SATOI MD

Kansai Medical University Hospita Department of Surgery

satoi@hirakata.kmu.ac.jp

Outcome results

None listed

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