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Neoadjuvant Triple Treatment with mFOLFIRINOX, pembrolizumab and SABR in patients with (borderline) resectable pancreatic cancer (PREOPANC-5): a multicenter single arm phase Ib/II trial of the Dutch Pancreatic Cancer Group

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-508707-20-00
Acronym
2023-508707-20-00
Enrollment
66
Registered
2024-04-29
Start date
2024-09-19
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

Borderline resectable pancreatic cancer (BRPC), Pancreatic cancer, Resectable pancreatic cancer (RPC)

Brief summary

Progression free survival, defined as the time from inclusion to the clinical trial to disease recurrence/progression or death from any cause

Detailed description

Overall survival, Resection rate, pR0 resection rate, Postoperative complications, Toxicity, Quality of life (QoL), Completion of neoadjuvant chemotherapy, Completion of neoadjuvant immunotherapy, Radiological response rate, Serum CA 19-9 response, Serum CEA response, Pathologic response, Immune responses, sR0 resection rate, Completion of adjuvant chemotherapy, Completion of neoadjuvant SABR, Completion of adjuvant immunotherapy, lymph node tumor-negative resection rate

Interventions

Sponsors

Amsterdam UMC
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Progression free survival, defined as the time from inclusion to the clinical trial to disease recurrence/progression or death from any cause

Secondary

MeasureTime frame
Overall survival, Resection rate, pR0 resection rate, Postoperative complications, Toxicity, Quality of life (QoL), Completion of neoadjuvant chemotherapy, Completion of neoadjuvant immunotherapy, Radiological response rate, Serum CA 19-9 response, Serum CEA response, Pathologic response, Immune responses, sR0 resection rate, Completion of adjuvant chemotherapy, Completion of neoadjuvant SABR, Completion of adjuvant immunotherapy, lymph node tumor-negative resection rate

Countries

Netherlands

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026