About this trial
The purpose of the study is to evaluate the efficacy and safety of NALIRINOX combined with PD-1 synchronous sequential SBRT or AG combined with PD-1 synchronous sequential SBRT as first line systematical therapy in patients with ocally advanced pancreatic cancer.
Eligibility criteria
Qualifiers
Histologically or cytologically confirmed pancreatic cancer;
ECOG performance no more than 2;
Radiographically assessed as locally advanced pancreatic cancer according to NCCN guidelines;
No previous anti-tumor therapy;
Disqualifiers
1. Prior anti-tumor therapy of any kind; 2. Severe infection (>NCI CTC grade 2); 3.Patients with autoimmune disease or immune deficiency who are treated with immunosuppressive drugs; 4.Patients with bleeding tendency; 5. Pregnant or lactating women.
Trial design
Treatments tested in this trial
- nal-IRI+Oxaliplatin+5-FU/LV+PD-1
- Gemcitabine + albumin-paclitaxel+PD-1
Treatment groups
Sponsors and collaborators
Du Juan
Lead sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
Sponsor institution