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S-1/irinotecan/oxaliplatin regimen in patients with with locally advanced or metastatic pancreatic adenocarcinoma

S-1/irinotecan/oxaliplatin regimen in patients with with locally advanced or metastatic pancreatic adenocarcinoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-17012827
Enrollment
Unknown
Registered
2017-09-28
Start date
2017-10-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

Pancreatic Adenocarcinoma

Interventions

Study group:SOXIRI chemotherapy

Sponsors

Fudan University Affiliated Huadong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75, men or women; 2. A histologically or cytologically proven diagnosis of pancreatic adenocarcinoma; 3. An eastern Cooperative Oncology Group (ECOG) performance status of 1 or less; 4. Without the history of chemotherapy or radiotherapy in six months; 5. Without severe hematological, cardiopulmonary, and immune disorders; 6. Absolute neutrophil count =1.5*10^9 /L, platelet count =100*10^9/L, hemoglobin =8g/L 7. Serum transaminases = 2.5*the upper normal limit (ULN), total bilirubin =1.5*ULN (in cases of biliary stent, total bilirubin =3.0*ULN) , alkaline phosphatase =2.5*ULN, serum creatinine =1.5*ULN; 8. Prothrombin time and International Normalized Ratio=1.5*ULN.

Exclusion criteria

Exclusion criteria: 1. The patient has been allergic to the medicines; 2. The patient has took part in other clinical trial at the same time; 3. The patient has received blood infusions or blood products within 15 days; 4. The patient has undergone major operation within 4 weeks; 5. The patient has gut dysfunction.

Design outcomes

Primary

MeasureTime frame
Objective response rate;

Secondary

MeasureTime frame
Overall survival;Progression-free survival;One year survival;

Countries

China

Contacts

Public ContactChongyi Jiang

Fudan University Affiliated Huadong Hospital

jiangzhongyi9@126.com+86 18101802916

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026