Pancreatic Cancer Clinical Trial
Official title:
Phase II Single Arm Clinical Trial of FOLFIRINOX for Unresectable Locally Advanced and Borderline Resectable Pancreatic Cancer
This single arm, multi-center phase II clinical trial will assess the safety and efficacy of FOLFIRINOX in the first-line setting in patients with unresectable locally advanced (ULA) and borderline resectable (BR) pancreatic cancer.
FOLFIRINOX regimen was recently presented at an international oncology meeting and represents
a new standard in the treatment of metastatic pancreatic cancer for selected patients. With
improved overall survival (OS) and response rates (RR) in the metastatic setting, we
hypothesize that in patients with less tumor burden, this regimen will be safe and well
tolerated, improve OS, progression free survival (PFS), and RR, and improve resectability
rates, as compared to historical data from standard single agent gemcitabine therapy for
unresectable locally advanced (ULA) patients and standard radiation with concurrent 5
fluorouracil (5FU) chemotherapy for borderline resectable (BR) patients. While both ULA and
BR patients will be eligible for the present study, our primary objective concerns ULA
patients, and we plan to enroll 45 patients in this group.
Patients meeting eligibility criteria will be consented and treated with FOLFIRINOX every 2
weeks (1 cycle = 4 weeks = 2 treatments). Patients will undergo repeat imaging (CT or MRI)
every 2 cycles and reassessed for resectability of the tumor. All patients that are not able
to undergo surgical resection, due to insufficient down-staging or patient preference, will
continue on protocol-based therapy until disease progression, unacceptable toxicity, study
withdrawal, or death.
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